geneid | 57835 |
---|---|
ensemblid | ENSG00000188687.18 |
hgncid | 18168 |
symbol | SLC4A5 |
name | solute carrier family 4 member 5 |
refseq_nuc | NM_133478.3 |
refseq_prot | NP_597812.1 |
ensembl_nuc | ENST00000394019.7 |
ensembl_prot | ENSP00000377587.2 |
mane_status | MANE Select |
chr | chr2 |
start | 74216242 |
end | 74343416 |
strand | - |
ver | v1.2 |
region | chr2:74216242-74343416 |
region5000 | chr2:74211242-74348416 |
regionname0 | SLC4A5_chr2_74216242_74343416 |
regionname5000 | SLC4A5_chr2_74211242_74348416 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1121 | 244 | 65 | 46 | 115 | 4 | 12 | 83 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002 | 0/0 | 1121 | 20 | 17 | 0 | 1 | 0 | 2 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0003 | 0/0 | 1121 | 14 | 0 | 2 | 10 | 0 | 2 | 9 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0004 | 0/0 | 1121 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0005 | 0/0 | 1121 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0006 | 0/0 | 1121 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0007 | 0/0 | 1121 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 3366 | 166 | 42 | 25 | 83 | 3 | 11 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0002 | 0/0 | 3366 | 41 | 8 | 17 | 15 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0003 | 0/0 | 3366 | 33 | 11 | 4 | 17 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0004 | 0/0 | 3366 | 18 | 15 | 0 | 1 | 0 | 2 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0005 | 0/0 | 3366 | 10 | 0 | 1 | 7 | 0 | 2 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0006 | 0/0 | 3366 | 3 | 0 | 1 | 2 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0007 | 0/0 | 3366 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0008 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0009 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0010 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0011 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0012 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0013 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0014 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0015 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
c0016 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2992 | 115 | 23 | 29 | 51 | 2 | 9 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0002 | 0/1 | 2992 | 60 | 5 | 9 | 39 | 0 | 6 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0003 | 0/0 | 2989 | 37 | 14 | 7 | 13 | 2 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0004 | 0/0 | 2989 | 9 | 9 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0005 | 0/0 | 2989 | 9 | 0 | 0 | 9 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0006 | 0/0 | 2992 | 7 | 0 | 0 | 7 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0007 | 0/0 | 2989 | 7 | 7 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0008 | 0/0 | 2992 | 7 | 6 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0009 | 0/0 | 2989 | 4 | 4 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0010 | 0/0 | 2992 | 3 | 3 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0011 | 0/0 | 2992 | 3 | 3 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0012 | 0/0 | 2992 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0013 | 0/0 | 2992 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0014 | 0/0 | 2989 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0015 | 0/0 | 2992 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0016 | 0/0 | 2992 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0017 | 0/0 | 2989 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0018 | 0/0 | 2989 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0019 | 0/0 | 2992 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0020 | 0/0 | 2989 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0021 | 0/0 | 2989 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0022 | 0/0 | 2992 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0023 | 0/0 | 2992 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0024 | 0/0 | 2992 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0025 | 0/0 | 2992 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0026 | 0/0 | 2992 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
t0027 | 0/0 | 2989 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0253 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3366 | 166 | 42 | 25 | 83 | 3 | 11 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0002 | 0/0 | 3366 | 41 | 8 | 17 | 15 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0003 | 0/0 | 3366 | 33 | 11 | 4 | 17 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0007 | 0/0 | 3366 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0013 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0014 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0004 | 0/0 | 3366 | 18 | 15 | 0 | 1 | 0 | 2 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0008 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0010 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0003c0005 | 0/0 | 3366 | 10 | 0 | 1 | 7 | 0 | 2 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0003c0006 | 0/0 | 3366 | 3 | 0 | 1 | 2 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0003c0016 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0004c0009 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0005c0012 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0006c0011 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0007c0015 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6357 | 57 | 8 | 14 | 27 | 2 | 5 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0002 | 0/1 | 6357 | 51 | 4 | 5 | 36 | 0 | 5 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0003 | 0/0 | 6354 | 13 | 1 | 3 | 7 | 1 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0004 | 0/0 | 6354 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0005 | 0/0 | 6354 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0006 | 0/0 | 6357 | 5 | 0 | 0 | 5 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0007 | 0/0 | 6354 | 5 | 5 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0008 | 0/0 | 6357 | 7 | 6 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0009 | 0/0 | 6354 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0010 | 0/0 | 6357 | 3 | 3 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0011 | 0/0 | 6357 | 3 | 3 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0012 | 0/0 | 6357 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0013 | 0/0 | 6357 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0015 | 0/0 | 6357 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0016 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0018 | 0/0 | 6354 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0019 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0020 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0021 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0022 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0023 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0024 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0025 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0026 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0001t0027 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0002t0001 | 0/0 | 6357 | 36 | 8 | 13 | 14 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0002t0002 | 0/0 | 6357 | 5 | 0 | 4 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0003t0001 | 0/0 | 6357 | 4 | 1 | 0 | 3 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0003t0003 | 0/0 | 6354 | 21 | 10 | 4 | 6 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0003t0005 | 0/0 | 6354 | 7 | 0 | 0 | 7 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0003t0017 | 0/0 | 6354 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0007t0004 | 0/0 | 6354 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0013t0003 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0001c0014t0001 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0004t0001 | 0/0 | 6357 | 6 | 4 | 0 | 0 | 0 | 2 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0004t0002 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0004t0003 | 0/0 | 6354 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0004t0004 | 0/0 | 6354 | 4 | 4 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0004t0007 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0004t0009 | 0/0 | 6354 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0004t0014 | 0/0 | 6354 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0008t0002 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0002c0010t0004 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0003c0005t0001 | 0/0 | 6357 | 6 | 0 | 1 | 4 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0003c0005t0002 | 0/0 | 6357 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0003c0005t0006 | 0/0 | 6357 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0003c0005t0012 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0003c0006t0001 | 0/0 | 6357 | 3 | 0 | 1 | 2 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0003c0016t0005 | 0/0 | 6354 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0004c0009t0007 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0005c0012t0002 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0006c0011t0001 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
a0007c0015t0001 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | copy fasta | chr2 | 74211242 | 74348416 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0253 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0006g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0006g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0010g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0012g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0013g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0013g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0015g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0016g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0018g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0019g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0020g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0021g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0022g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0023g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0024g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0025g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0026g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0001t0027g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0003t0017g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0007t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0007t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0013t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0001c0014t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0009g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0014g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0004t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0008t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0002c0010t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0005t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0005t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0005t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0005t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0005t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0005t0012g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0006t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0006t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0006t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0003c0016t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0004c0009t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0005c0012t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0006c0011t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
a0007c0015t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | FIN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00280 | hp2 | a0001 | c0003 | t0003 | g0208 | EUR | FIN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00438 | hp1 | a0001 | c0003 | t0003 | g0280 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0074 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00544 | hp2 | a0005 | c0012 | t0002 | g0041 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00597 | hp2 | a0001 | c0001 | t0013 | g0019 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00609 | hp2 | a0001 | c0001 | t0012 | g0212 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00621 | hp2 | a0003 | c0005 | t0006 | g0281 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00673 | hp1 | a0001 | c0003 | t0003 | g0071 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00735 | hp1 | a0001 | c0001 | t0018 | g0004 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01106 | hp1 | a0001 | c0003 | t0003 | g0012 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01109 | hp1 | a0001 | c0001 | t0008 | g0263 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0149 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0257 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0259 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01169 | hp2 | a0001 | c0003 | t0003 | g0206 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01257 | hp1 | a0001 | c0003 | t0003 | g0242 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0046 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0083 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0132 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01433 | hp2 | a0001 | c0001 | t0022 | g0197 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01884 | hp1 | a0001 | c0001 | t0011 | g0103 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01884 | hp2 | a0001 | c0013 | t0003 | g0153 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01891 | hp1 | a0007 | c0015 | t0001 | g0164 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0151 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0134 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01981 | hp1 | a0003 | c0005 | t0001 | g0227 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01981 | hp2 | a0003 | c0006 | t0001 | g0241 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02040 | hp2 | a0001 | c0003 | t0003 | g0078 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02055 | hp1 | a0002 | c0004 | t0009 | g0262 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02071 | hp1 | a0001 | c0001 | t0012 | g0051 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0127 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02135 | hp1 | a0001 | c0003 | t0003 | g0037 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0159 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0233 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02155 | hp2 | a0001 | c0001 | t0025 | g0031 | EAS | CDX | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CDX | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | CDX | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02257 | hp1 | a0001 | c0001 | t0011 | g0162 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02257 | hp2 | a0004 | c0009 | t0007 | g0106 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0238 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0188 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0183 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02451 | hp2 | a0001 | c0001 | t0015 | g0101 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02523 | hp2 | a0001 | c0001 | t0024 | g0141 | EAS | KHV | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02572 | hp1 | a0001 | c0003 | t0003 | g0276 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0122 | SAS | PJL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0193 | SAS | PJL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02615 | hp1 | a0002 | c0004 | t0004 | g0170 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02622 | hp1 | a0001 | c0003 | t0003 | g0274 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02622 | hp2 | a0002 | c0004 | t0014 | g0254 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02630 | hp1 | a0001 | c0003 | t0003 | g0156 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02647 | hp1 | a0002 | c0004 | t0001 | g0104 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02717 | hp1 | a0001 | c0001 | t0019 | g0161 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02735 | hp2 | a0002 | c0004 | t0001 | g0271 | SAS | PJL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02809 | hp1 | a0001 | c0003 | t0003 | g0215 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02809 | hp2 | a0002 | c0004 | t0014 | g0256 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02895 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02922 | hp1 | a0001 | c0003 | t0003 | g0245 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02965 | hp1 | a0002 | c0004 | t0004 | g0171 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02965 | hp2 | a0001 | c0001 | t0026 | g0107 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02970 | hp1 | a0002 | c0004 | t0001 | g0173 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0100 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02976 | hp1 | a0001 | c0003 | t0003 | g0234 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0189 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03041 | hp1 | a0001 | c0001 | t0027 | g0010 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03041 | hp2 | a0001 | c0001 | t0021 | g0261 | AFR | GWD | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03098 | hp1 | a0002 | c0008 | t0002 | g0167 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03098 | hp2 | a0001 | c0001 | t0010 | g0278 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03130 | hp1 | a0002 | c0010 | t0004 | g0105 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0191 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0186 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03195 | hp2 | a0002 | c0004 | t0004 | g0166 | AFR | ESN | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03209 | hp1 | a0001 | c0003 | t0003 | g0007 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03209 | hp2 | a0001 | c0001 | t0011 | g0190 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03453 | hp1 | a0001 | c0001 | t0016 | g0003 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03453 | hp2 | a0001 | c0001 | t0020 | g0029 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03486 | hp1 | a0002 | c0004 | t0007 | g0255 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03486 | hp2 | a0001 | c0001 | t0010 | g0279 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0187 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03654 | hp1 | a0003 | c0005 | t0001 | g0085 | SAS | PJL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03654 | hp2 | a0002 | c0004 | t0001 | g0277 | SAS | PJL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18522 | hp2 | a0001 | c0001 | t0015 | g0102 | AFR | YRI | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | CHB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18747 | hp2 | a0001 | c0003 | t0017 | g0020 | EAS | CHB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | YRI | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18906 | hp2 | a0002 | c0004 | t0004 | g0172 | AFR | YRI | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18939 | hp1 | a0003 | c0006 | t0001 | g0079 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18941 | hp2 | a0001 | c0003 | t0005 | g0179 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18942 | hp1 | a0003 | c0016 | t0005 | g0060 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18943 | hp1 | a0001 | c0003 | t0005 | g0177 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18951 | hp2 | a0003 | c0005 | t0012 | g0089 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18952 | hp1 | a0003 | c0005 | t0001 | g0072 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18952 | hp2 | a0001 | c0003 | t0005 | g0181 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18957 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18974 | hp2 | a0001 | c0003 | t0005 | g0178 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18977 | hp2 | a0001 | c0001 | t0023 | g0055 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18981 | hp1 | a0001 | c0003 | t0005 | g0182 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18987 | hp2 | a0001 | c0001 | t0006 | g0236 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0272 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19002 | hp1 | a0003 | c0005 | t0001 | g0088 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19002 | hp2 | a0001 | c0001 | t0006 | g0247 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19009 | hp2 | a0001 | c0003 | t0003 | g0094 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19012 | hp2 | a0003 | c0006 | t0001 | g0076 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19030 | hp1 | a0002 | c0004 | t0001 | g0219 | AFR | LWK | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19030 | hp2 | a0001 | c0007 | t0004 | g0008 | AFR | LWK | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | LWK | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | LWK | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19057 | hp1 | a0003 | c0005 | t0001 | g0070 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19058 | hp1 | a0001 | c0003 | t0003 | g0224 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19062 | hp2 | a0001 | c0003 | t0001 | g0028 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19066 | hp1 | a0006 | c0011 | t0001 | g0035 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19070 | hp1 | a0003 | c0005 | t0001 | g0077 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19079 | hp1 | a0001 | c0003 | t0005 | g0180 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19082 | hp1 | a0001 | c0001 | t0013 | g0018 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19082 | hp2 | a0001 | c0003 | t0005 | g0175 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19085 | hp1 | a0002 | c0004 | t0002 | g0210 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19087 | hp1 | a0003 | c0005 | t0006 | g0087 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0258 | AFR | YRI | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA19240 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | YRI | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ASW | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA20129 | hp2 | a0001 | c0007 | t0004 | g0006 | AFR | ASW | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0267 | EUR | TSI | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | TSI | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA20905 | hp1 | a0003 | c0005 | t0002 | g0252 | SAS | GIH | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | GIH | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG01123 | hp2 | a0001 | c0003 | t0003 | g0081 | AMR | CLM | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02486 | hp1 | a0002 | c0004 | t0003 | g0169 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02486 | hp2 | a0002 | c0004 | t0001 | g0202 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0110 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG02559 | hp2 | a0001 | c0003 | t0003 | g0144 | AFR | ACB | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG03471 | hp2 | a0001 | c0001 | t0007 | g0163 | AFR | MSL | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG06807 | hp1 | a0001 | c0003 | t0003 | g0246 | AFR | USA | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
HG06807 | hp2 | a0002 | c0004 | t0003 | g0168 | AFR | USA | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0158 | AFR | USA | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA20300 | hp2 | a0002 | c0004 | t0009 | g0270 | AFR | USA | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
NA21309 | hp2 | a0001 | c0014 | t0001 | g0265 | AFR | LWK | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0009 | REF | REF | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0253 | REF | REF | SLC4A5_chr2_74211242_74348416 | SLC4A5 | chr2 | 74211242 | 74348416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74231302
|
C | A | 1 | a0006 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.2781G>T | p.Gln927His | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/31 | 3188/6357 | 2781/3366 | 927/1121 | chr2 | 74231302 | ||
chr2:74233529
|
G | A | 1 | a0004 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.2468C>T | p.Pro823Leu | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 23/31 | 2875/6357 | 2468/3366 | 823/1121 | chr2 | 74233529 | ||
chr2:74239348
|
T | C | 1 | a0005 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.2306A>G | p.Tyr769Cys | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/31 | 2713/6357 | 2306/3366 | 769/1121 | chr2 | 74239348 | ||
chr2:74250504
|
G | C | 1 | a0007 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1492C>G | p.Leu498Val | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/31 | 1899/6357 | 1492/3366 | 498/1121 | chr2 | 74250504 | ||
chr2:74262191
|
G | A | 1 | a0003 | 14 | HG00621.hp2 HG01981.hp1 HG01981.hp2 others(11): Show |
missense_variant | MODERATE | c.757C>T | p.His253Tyr | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/31 | 1164/6357 | 757/3366 | 253/1121 | chr2 | 74262191 | ||
chr2:74262196
|
C | T | 2 | a0002a0004 | 21 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(18): Show |
missense_variant | MODERATE | c.752G>A | p.Ser251Asn | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/31 | 1159/6357 | 752/3366 | 251/1121 | chr2 | 74262196 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74222932
|
C | T | 1 | a0001c0013 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.3267G>A | p.Ser1089Ser | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/31 | 3674/6357 | 3267/3366 | 1089/1121 | chr2 | 74222932 | ||
chr2:74224846
|
A | G | 1 | a0001c0014 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.3240T>C | p.Asp1080Asp | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/31 | 3647/6357 | 3240/3366 | 1080/1121 | chr2 | 74224846 | ||
chr2:74231239
|
T | C | 1 | a0002c0008 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.2844A>G | p.Leu948Leu | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/31 | 3251/6357 | 2844/3366 | 948/1121 | chr2 | 74231239 | ||
chr2:74231293
|
G | A | 2 | a0001c0007a0002c0010 | 3 | HG03130.hp1 NA19030.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.2790C>T | p.Thr930Thr | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/31 | 3197/6357 | 2790/3366 | 930/1121 | chr2 | 74231293 | ||
chr2:74233558
|
C | T | 2 | a0001c0002a0003c0006 | 44 | HG00558.hp2 HG00597.hp1 HG00741.hp1 others(41): Show |
synonymous_variant | LOW | c.2439G>A | p.Thr813Thr | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 23/31 | 2846/6357 | 2439/3366 | 813/1121 | chr2 | 74233558 | ||
chr2:74239467
|
G | A | 5 | a0001c0003a0001c0007a0001c0013others(2): Show | 38 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(35): Show |
synonymous_variant | LOW | c.2187C>T | p.Gly729Gly | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/31 | 2594/6357 | 2187/3366 | 729/1121 | chr2 | 74239467 | ||
chr2:74247049
|
G | A | 1 | a0001c0014 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2046C>T | p.Val682Val | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/31 | 2453/6357 | 2046/3366 | 682/1121 | chr2 | 74247049 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74216307
|
A | G | 7 | a0001c0001t0007a0001c0001t0009a0001c0001t0027others(4): Show | 14 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2519T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 5160 | chr2 | 74216307 | |||||
chr2:74216341
|
T | C | 1 | a0001c0001t0023 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2485A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 5126 | chr2 | 74216341 | |||||
chr2:74216342
|
G | A | 2 | a0001c0001t0018a0001c0001t0020 | 2 | HG00735.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2484C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 5125 | chr2 | 74216342 | |||||
chr2:74216483
|
A | G | 4 | a0001c0001t0011a0001c0001t0018a0001c0001t0020others(1): Show | 6 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2343T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 4984 | chr2 | 74216483 | |||||
chr2:74216508
|
G | A | 2 | a0001c0001t0012a0003c0005t0012 | 3 | HG00609.hp2 HG02071.hp1 NA18951.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2318C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 4959 | chr2 | 74216508 | |||||
chr2:74216603
|
T | A | 1 | a0001c0001t0025 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2223A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 4864 | chr2 | 74216603 | |||||
chr2:74216634
|
G | A | 1 | a0001c0001t0015 | 2 | HG02451.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2192C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 4833 | chr2 | 74216634 | |||||
chr2:74216856
|
C | T | 1 | a0001c0001t0008 | 7 | HG01109.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1970G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 4611 | chr2 | 74216856 | |||||
chr2:74217102
|
C | T | 2 | a0001c0001t0010a0001c0001t0019 | 4 | HG02717.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1724G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 4365 | chr2 | 74217102 | |||||
chr2:74217174
|
T | G | 7 | a0001c0001t0007a0001c0001t0009a0001c0001t0027others(4): Show | 14 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1652A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 4293 | chr2 | 74217174 | |||||
chr2:74217304
|
A | T | 9 | a0001c0001t0003a0001c0001t0005a0001c0001t0024others(6): Show | 48 | HG00280.hp2 HG00438.hp1 HG00673.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1522T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 4163 | chr2 | 74217304 | |||||
chr2:74217796
|
G | A | 1 | a0002c0004t0014 | 2 | HG02622.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1030C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 3671 | chr2 | 74217796 | |||||
chr2:74217881
|
G | A | 3 | a0001c0001t0005a0001c0003t0005a0003c0016t0005 | 9 | NA18941.hp2 NA18942.hp1 NA18943.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*945C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 3586 | chr2 | 74217881 | |||||
chr2:74217908
|
A | G | 8 | a0001c0001t0002a0001c0001t0013a0001c0001t0023others(5): Show | 63 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*918T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 3559 | chr2 | 74217908 | |||||
chr2:74217919
|
T | A | 1 | a0001c0001t0021 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*907A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 3548 | chr2 | 74217919 | |||||
chr2:74217951
|
A | G | 2 | a0001c0001t0009a0002c0004t0009 | 4 | HG02055.hp1 HG02976.hp2 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*875T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 3516 | chr2 | 74217951 | |||||
chr2:74217965
|
G | A | 1 | a0001c0001t0026 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*861C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 3502 | chr2 | 74217965 | |||||
chr2:74218224
|
A | G | 1 | a0001c0001t0022 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*602T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 3243 | chr2 | 74218224 | |||||
chr2:74218234
|
T | G | 1 | a0001c0001t0021 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*592A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 3233 | chr2 | 74218234 | |||||
chr2:74218289
|
TTGA | T | 22 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(19): Show | 73 | HG00280.hp2 HG00438.hp1 HG00673.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*534_*536delTCA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 3175 | chr2 | 74218289 | |||||
chr2:74218508
|
A | G | 2 | a0001c0001t0006a0003c0005t0006 | 7 | HG00621.hp2 HG02083.hp2 NA18957.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*318T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 2959 | chr2 | 74218508 | |||||
chr2:74218685
|
T | C | 1 | a0001c0001t0027 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*141A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 31/31 | 2782 | chr2 | 74218685 | |||||
chr2:74221437
|
C | T | 1 | a0001c0001t0019 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/31 | 30 | chr2 | 74221437 | |||||
chr2:74334126
|
C | T | 1 | a0001c0001t0018 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-169G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/31 | 19103 | chr2 | 74334126 | |||||
chr2:74334133
|
A | G | 2 | a0001c0001t0013a0001c0003t0017 | 3 | HG00597.hp2 NA18747.hp2 NA19082.hp1 |
5_prime_UTR_variant | MODIFIER | c.-176T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/31 | 19110 | chr2 | 74334133 | |||||
chr2:74342507
|
C | G | 1 | a0001c0001t0016 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-319G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/31 | 27484 | chr2 | 74342507 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74218885
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(273): Show | 277 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.*34-93A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74218885 | ||||||
chr2:74219161
|
T | A | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.*34-369A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219161 | ||||||
chr2:74219176
|
G | GGT | 14 | a0001c0001t0001g0200a0001c0001t0001g0209a0001c0001t0001g0230others(11): Show | 14 | HG00597.hp2 HG00741.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.*34-386_*34-385dup others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219176 | ||||||
chr2:74219176
|
G | GGTGT | 6 | a0001c0001t0001g0091a0001c0001t0002g0014a0001c0001t0002g0015others(3): Show | 6 | HG00609.hp1 HG03130.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.*34-388_*34-385dup others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219176 | ||||||
chr2:74219176
|
G | GGTGTGTG others(3): Show |
1 | a0001c0001t0002g0062 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.*34-394_*34-385dup others(10): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219176 | ||||||
chr2:74219176
|
GGT | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(86): Show | 90 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.*34-386_*34-385del others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219176 | ||||||
chr2:74219176
|
GGTGT | G | 12 | a0001c0001t0001g0034a0001c0001t0001g0109a0001c0001t0001g0160others(9): Show | 12 | HG02257.hp1 HG02486.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.*34-388_*34-385del others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219176 | ||||||
chr2:74219176
|
GGTGTGT | G | 4 | a0001c0001t0008g0183a0001c0001t0008g0258a0001c0001t0008g0263others(1): Show | 4 | HG01109.hp1 HG02145.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.*34-390_*34-385del others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219176 | ||||||
chr2:74219176
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0080a0002c0004t0001g0219 | 2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.*34-394_*34-385del others(10): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219176 | ||||||
chr2:74219176
|
GGTGTGTG others(5): Show |
G | 2 | a0001c0003t0001g0028a0001c0003t0001g0042 | 2 | NA19000.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.*34-396_*34-385del others(12): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219176 | ||||||
chr2:74219176
|
GGTGTGTG others(7): Show |
G | 1 | a0001c0001t0002g0059 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.*34-398_*34-385del others(14): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219176 | ||||||
chr2:74219201
|
GTGTGTGT others(13): Show |
G | 9 | a0001c0001t0003g0260a0001c0001t0007g0016a0001c0001t0007g0158others(6): Show | 9 | HG01884.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.*34-429_*34-410del others(20): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219201 | ||||||
chr2:74219203
|
GTGTGTGT others(11): Show |
G | 12 | a0001c0001t0004g0157a0001c0001t0007g0155a0001c0001t0007g0163others(9): Show | 12 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.*34-429_*34-412del others(18): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219203 | ||||||
chr2:74219207
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0004g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*34-429_*34-416del others(14): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219207 | ||||||
chr2:74219209
|
GTGTGTGT others(5): Show |
G | 3 | a0001c0001t0005g0272a0001c0002t0001g0143a0001c0003t0005g0182 | 3 | NA18747.hp1 NA18981.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.*34-429_*34-418del others(12): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219209 | ||||||
chr2:74219211
|
GTGTGTGT others(3): Show |
G | 29 | a0001c0001t0001g0220a0001c0001t0001g0248a0001c0001t0003g0193others(26): Show | 29 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.*34-429_*34-420del others(10): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219211 | ||||||
chr2:74219213
|
G | T | 2 | a0001c0001t0001g0196a0001c0001t0022g0197 | 2 | HG01070.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.*34-421C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219213 | ||||||
chr2:74219213
|
GTGTGTGT others(1): Show |
G | 27 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0001t0003g0184others(24): Show | 27 | HG00438.hp1 HG01081.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.*34-429_*34-422del others(8): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219213 | ||||||
chr2:74219215
|
GTGTGTT | G | 23 | a0001c0001t0003g0032a0001c0001t0003g0045a0001c0001t0003g0203others(20): Show | 23 | HG00673.hp1 HG00735.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.*34-429_*34-424del others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219215 | ||||||
chr2:74219217
|
GTGTT | G | 10 | a0001c0001t0002g0050a0001c0001t0003g0061a0001c0001t0003g0194others(7): Show | 10 | HG00280.hp2 HG01123.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.*34-429_*34-426del others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219217 | ||||||
chr2:74219219
|
GTT | G | 3 | a0001c0002t0001g0111a0001c0003t0003g0206a0001c0003t0003g0274 | 3 | HG00741.hp1 HG01169.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.*34-429_*34-428del others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219219 | ||||||
chr2:74219221
|
T | G | 2 | a0001c0007t0004g0008a0002c0010t0004g0105 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.*34-429A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219221 | ||||||
chr2:74219246
|
C | T | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.*34-454G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219246 | ||||||
chr2:74219282
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.*34-490A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219282 | ||||||
chr2:74219361
|
A | G | 119 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0001t0001g0220others(116): Show | 119 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.*34-569T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219361 | ||||||
chr2:74219442
|
TG | T | 41 | a0001c0001t0001g0220a0001c0001t0001g0248a0001c0002t0001g0005others(38): Show | 41 | HG00558.hp2 HG00597.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.*34-651delC | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219442 | ||||||
chr2:74219452
|
T | C | 1 | a0001c0002t0001g0142 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.*34-660A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219452 | ||||||
chr2:74219832
|
G | C | 1 | a0001c0001t0001g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*34-1040C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219832 | ||||||
chr2:74219880
|
G | A | 1 | a0001c0003t0001g0233 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.*34-1088C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219880 | ||||||
chr2:74219914
|
G | C | 1 | a0001c0001t0003g0193 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.*34-1122C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219914 | ||||||
chr2:74219989
|
C | G | 1 | a0002c0008t0002g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*34-1197G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219989 | ||||||
chr2:74219997
|
G | A | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.*34-1205C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74219997 | ||||||
chr2:74220042
|
T | C | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*34-1250A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220042 | ||||||
chr2:74220126
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.*33+1308C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220126 | ||||||
chr2:74220201
|
C | T | 3 | a0001c0002t0001g0151a0001c0002t0001g0238a0003c0006t0001g0241 | 3 | HG01952.hp2 HG01981.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.*33+1233G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220201 | ||||||
chr2:74220237
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.*33+1197G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220237 | ||||||
chr2:74220238
|
G | A | 1 | a0001c0003t0003g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*33+1196C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220238 | ||||||
chr2:74220327
|
A | AGTTGATC others(18): Show |
3 | a0001c0001t0008g0258a0001c0001t0008g0263a0001c0001t0011g0162 | 3 | HG01109.hp1 HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.*33+1082_*33+1106d others(27): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220327 | ||||||
chr2:74220327
|
A | AGTTGATC others(43): Show |
1 | a0001c0001t0011g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.*33+1106_*33+1107i others(52): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220327 | ||||||
chr2:74220440
|
G | C | 6 | a0001c0001t0008g0183a0001c0001t0015g0101a0001c0001t0015g0102others(3): Show | 6 | HG00735.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.*33+994C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220440 | ||||||
chr2:74220472
|
C | A | 1 | a0001c0001t0004g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*33+962G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220472 | ||||||
chr2:74220527
|
C | T | 1 | a0001c0002t0001g0207 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.*33+907G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220527 | ||||||
chr2:74220547
|
T | C | 1 | a0002c0008t0002g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*33+887A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220547 | ||||||
chr2:74220555
|
T | C | 4 | a0001c0007t0004g0006a0001c0007t0004g0008a0002c0008t0002g0167others(1): Show | 4 | HG03098.hp1 HG03130.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.*33+879A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220555 | ||||||
chr2:74220577
|
C | T | 39 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0002t0001g0005others(36): Show | 39 | HG00558.hp2 HG00597.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.*33+857G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220577 | ||||||
chr2:74220579
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.*33+855A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220579 | ||||||
chr2:74220579
|
T | G | 1 | a0002c0004t0007g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*33+855A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220579 | ||||||
chr2:74220610
|
A | G | 1 | a0002c0008t0002g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.*33+824T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220610 | ||||||
chr2:74220618
|
G | A | 1 | a0003c0005t0001g0077 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.*33+816C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220618 | ||||||
chr2:74220625
|
TCCTGCCT others(317): Show |
T | 3 | a0001c0001t0011g0103a0001c0001t0011g0162a0001c0001t0011g0190 | 3 | HG01884.hp1 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.*33+485_*33+808del | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220625 | ||||||
chr2:74220655
|
T | C | 175 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(172): Show | 175 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.*33+779A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220655 | ||||||
chr2:74220758
|
T | C | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.*33+676A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220758 | ||||||
chr2:74220762
|
C | T | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.*33+672G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220762 | ||||||
chr2:74220768
|
A | G | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.*33+666T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220768 | ||||||
chr2:74220795
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.*33+639G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220795 | ||||||
chr2:74220806
|
G | A | 2 | a0001c0002t0001g0046a0001c0002t0001g0185 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.*33+628C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220806 | ||||||
chr2:74220841
|
C | CT | 10 | a0001c0001t0001g0192a0001c0001t0007g0016a0001c0001t0007g0158others(7): Show | 10 | HG02145.hp1 HG02258.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.*33+592dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220841 | ||||||
chr2:74220841
|
CT | C | 119 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(116): Show | 119 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.*33+592delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220841 | ||||||
chr2:74220879
|
T | C | 4 | a0001c0001t0010g0002a0001c0001t0010g0278a0001c0001t0010g0279others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*33+555A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220879 | ||||||
chr2:74220902
|
G | A | 1 | a0001c0001t0002g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.*33+532C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220902 | ||||||
chr2:74220904
|
G | T | 4 | a0001c0001t0010g0002a0001c0001t0010g0278a0001c0001t0010g0279others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.*33+530C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220904 | ||||||
chr2:74220966
|
T | G | 1 | a0001c0001t0004g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*33+468A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220966 | ||||||
chr2:74220986
|
C | G | 26 | a0001c0002t0001g0046a0001c0002t0001g0065a0001c0002t0001g0066others(23): Show | 26 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.*33+448G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74220986 | ||||||
chr2:74221169
|
T | C | 1 | a0001c0002t0001g0122 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.*33+265A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74221169 | ||||||
chr2:74221179
|
T | C | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*33+255A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74221179 | ||||||
chr2:74221290
|
G | C | 5 | a0001c0003t0003g0007a0001c0003t0003g0156a0001c0013t0003g0153others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.*33+144C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74221290 | ||||||
chr2:74221300
|
G | C | 2 | a0001c0002t0001g0046a0001c0002t0001g0185 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.*33+134C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74221300 | ||||||
chr2:74221357
|
A | G | 5 | a0001c0003t0003g0007a0001c0003t0003g0156a0001c0013t0003g0153others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.*33+77T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74221357 | ||||||
chr2:74221379
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.*33+55C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 30/30 | chr2 | 74221379 | ||||||
chr2:74221528
|
T | C | 37 | a0001c0001t0002g0043a0001c0001t0003g0032a0001c0001t0003g0203others(34): Show | 37 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.3332-27A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74221528 | ||||||
chr2:74221545
|
C | A | 76 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0002g0009others(73): Show | 76 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3332-44G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74221545 | ||||||
chr2:74221699
|
G | C | 3 | a0001c0001t0008g0017a0001c0001t0008g0096a0001c0001t0008g0100 | 3 | HG02895.hp1 HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3332-198C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74221699 | ||||||
chr2:74221786
|
G | T | 62 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0002g0009others(59): Show | 62 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.3332-285C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74221786 | ||||||
chr2:74221953
|
C | G | 38 | a0001c0002t0001g0005a0001c0002t0001g0021a0001c0002t0001g0046others(35): Show | 38 | HG00558.hp2 HG00597.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.3332-452G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74221953 | ||||||
chr2:74222024
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3332-523A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74222024 | ||||||
chr2:74222175
|
G | A | 76 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0002g0009others(73): Show | 76 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.3332-674C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74222175 | ||||||
chr2:74222457
|
C | A | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3331+411G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74222457 | ||||||
chr2:74222514
|
A | G | 2 | a0002c0004t0014g0254a0002c0004t0014g0256 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3331+354T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74222514 | ||||||
chr2:74222543
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3331+325G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74222543 | ||||||
chr2:74222630
|
C | T | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3331+238G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74222630 | ||||||
chr2:74222750
|
G | T | 1 | a0001c0001t0006g0236 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3331+118C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74222750 | ||||||
chr2:74222775
|
A | T | 1 | a0001c0002t0001g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3331+93T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 29/30 | chr2 | 74222775 | ||||||
chr2:74222998
|
T | C | 137 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(134): Show | 137 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.3247-46A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74222998 | ||||||
chr2:74223007
|
C | CT | 9 | a0001c0001t0001g0011a0001c0001t0004g0157a0001c0001t0008g0017others(6): Show | 9 | HG00438.hp2 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3247-56dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74223007 | ||||||
chr2:74223299
|
G | A | 53 | a0001c0001t0001g0034a0001c0001t0002g0009a0001c0001t0002g0014others(50): Show | 53 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.3247-347C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74223299 | ||||||
chr2:74223486
|
T | G | 5 | a0001c0001t0011g0103a0001c0001t0011g0162a0001c0001t0011g0190others(2): Show | 5 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.3247-534A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74223486 | ||||||
chr2:74223611
|
T | C | 1 | a0001c0002t0001g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3247-659A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74223611 | ||||||
chr2:74223927
|
C | G | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3246+913G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74223927 | ||||||
chr2:74223927
|
C | T | 1 | a0001c0003t0003g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3246+913G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74223927 | ||||||
chr2:74223963
|
T | G | 5 | a0001c0001t0007g0016a0001c0001t0007g0158a0001c0001t0007g0159others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3246+877A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74223963 | ||||||
chr2:74224351
|
C | T | 9 | a0001c0001t0004g0264a0001c0001t0021g0261a0001c0007t0004g0006others(6): Show | 9 | HG02615.hp1 HG02965.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.3246+489G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74224351 | ||||||
chr2:74224460
|
C | G | 1 | a0001c0002t0002g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3246+380G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74224460 | ||||||
chr2:74224560
|
C | T | 1 | a0001c0001t0006g0211 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.3246+280G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74224560 | ||||||
chr2:74224603
|
T | G | 1 | a0001c0002t0001g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3246+237A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74224603 | ||||||
chr2:74224635
|
C | T | 34 | a0001c0001t0002g0043a0001c0001t0003g0032a0001c0001t0003g0203others(31): Show | 34 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.3246+205G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74224635 | ||||||
chr2:74224820
|
C | T | 4 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0068others(1): Show | 5 | NA18943.hp2 NA18970.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.3246+20G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 28/30 | chr2 | 74224820 | ||||||
chr2:74225132
|
C | T | 6 | a0001c0001t0001g0200a0001c0001t0001g0250a0001c0001t0001g0266others(3): Show | 6 | HG01167.hp1 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3091-137G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74225132 | ||||||
chr2:74225200
|
G | A | 69 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0002g0009others(66): Show | 69 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.3091-205C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74225200 | ||||||
chr2:74225244
|
G | T | 2 | a0002c0004t0001g0202a0002c0004t0001g0277 | 2 | HG02486.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.3091-249C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74225244 | ||||||
chr2:74225410
|
A | G | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3091-415T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74225410 | ||||||
chr2:74225416
|
T | C | 1 | a0001c0001t0004g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3091-421A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74225416 | ||||||
chr2:74225568
|
C | T | 1 | a0001c0001t0012g0051 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3091-573G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74225568 | ||||||
chr2:74225594
|
T | G | 4 | a0001c0001t0010g0002a0001c0001t0010g0278a0001c0001t0010g0279others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3091-599A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74225594 | ||||||
chr2:74225595
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3091-600G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74225595 | ||||||
chr2:74225887
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3091-892G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74225887 | ||||||
chr2:74225919
|
G | A | 1 | a0001c0001t0003g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3091-924C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74225919 | ||||||
chr2:74226021
|
C | T | 9 | a0001c0001t0004g0264a0001c0001t0021g0261a0001c0007t0004g0006others(6): Show | 9 | HG02615.hp1 HG02965.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.3090+936G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74226021 | ||||||
chr2:74226034
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0230 | 2 | HG00741.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.3090+923C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74226034 | ||||||
chr2:74226076
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3090+881T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74226076 | ||||||
chr2:74226180
|
CAGCCCGG others(17): Show |
C | 1 | a0001c0002t0001g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3090+753_3090+776d others(26): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74226180 | ||||||
chr2:74226309
|
A | C | 7 | a0001c0002t0001g0083a0001c0002t0001g0111a0001c0002t0001g0112others(4): Show | 7 | HG00741.hp1 HG01261.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.3090+648T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74226309 | ||||||
chr2:74226519
|
G | A | 1 | a0001c0003t0003g0234 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3090+438C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74226519 | ||||||
chr2:74226641
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.3090+316T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74226641 | ||||||
chr2:74226836
|
G | A | 2 | a0001c0001t0018g0004a0001c0001t0020g0029 | 2 | HG00735.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3090+121C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74226836 | ||||||
chr2:74226859
|
A | G | 55 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0001t0004g0157others(52): Show | 55 | HG00558.hp2 HG00597.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.3090+98T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 27/30 | chr2 | 74226859 | ||||||
chr2:74227164
|
A | G | 57 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0001t0004g0157others(54): Show | 57 | HG00558.hp2 HG00597.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.2917-34T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 26/30 | chr2 | 74227164 | ||||||
chr2:74227321
|
G | C | 74 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0002g0009others(71): Show | 74 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.2917-191C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 26/30 | chr2 | 74227321 | ||||||
chr2:74227498
|
G | A | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2916+312C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 26/30 | chr2 | 74227498 | ||||||
chr2:74227556
|
G | A | 1 | a0001c0001t0002g0120 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2916+254C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 26/30 | chr2 | 74227556 | ||||||
chr2:74227614
|
G | C | 1 | a0001c0001t0001g0228 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2916+196C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 26/30 | chr2 | 74227614 | ||||||
chr2:74227703
|
G | A | 1 | a0001c0001t0002g0131 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2916+107C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 26/30 | chr2 | 74227703 | ||||||
chr2:74227720
|
G | T | 1 | a0001c0003t0005g0175 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2916+90C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 26/30 | chr2 | 74227720 | ||||||
chr2:74227759
|
A | T | 1 | a0001c0002t0002g0126 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2916+51T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 26/30 | chr2 | 74227759 | ||||||
chr2:74227789
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2916+21C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 26/30 | chr2 | 74227789 | ||||||
chr2:74227915
|
T | C | 4 | a0001c0001t0010g0002a0001c0001t0010g0278a0001c0001t0010g0279others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2848-37A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74227915 | ||||||
chr2:74227954
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0007t0004g0006others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2848-76G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74227954 | ||||||
chr2:74227995
|
G | A | 39 | a0001c0002t0001g0005a0001c0002t0001g0021a0001c0002t0001g0046others(36): Show | 39 | HG00558.hp2 HG00597.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2848-117C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74227995 | ||||||
chr2:74228162
|
C | T | 38 | a0001c0001t0003g0203a0001c0001t0024g0141a0001c0003t0001g0028others(35): Show | 38 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2848-284G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228162 | ||||||
chr2:74228345
|
C | T | 37 | a0001c0001t0003g0203a0001c0001t0024g0141a0001c0003t0001g0028others(34): Show | 37 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.2848-467G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228345 | ||||||
chr2:74228499
|
A | G | 140 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(137): Show | 140 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.2848-621T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228499 | ||||||
chr2:74228559
|
G | T | 1 | a0003c0005t0002g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2848-681C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228559 | ||||||
chr2:74228571
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2848-693C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228571 | ||||||
chr2:74228643
|
C | A | 5 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0007t0004g0006others(2): Show | 5 | HG01192.hp1 HG02572.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2848-765G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228643 | ||||||
chr2:74228653
|
A | G | 4 | a0001c0001t0008g0017a0001c0001t0008g0096a0001c0001t0008g0100others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2848-775T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228653 | ||||||
chr2:74228655
|
C | A | 2 | a0001c0002t0001g0021a0001c0002t0001g0092 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2848-777G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228655 | ||||||
chr2:74228668
|
C | A | 139 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(136): Show | 139 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.2848-790G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228668 | ||||||
chr2:74228676
|
C | A | 1 | a0001c0003t0005g0175 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2848-798G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228676 | ||||||
chr2:74228677
|
C | CA | 5 | a0001c0001t0011g0103a0001c0001t0011g0162a0001c0001t0011g0190others(2): Show | 5 | HG00735.hp1 HG01884.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.2848-800dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228677 | ||||||
chr2:74228686
|
A | C | 13 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0001t0004g0264others(10): Show | 13 | HG01192.hp1 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2848-808T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228686 | ||||||
chr2:74228911
|
G | A | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2848-1033C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74228911 | ||||||
chr2:74229021
|
G | A | 1 | a0001c0003t0001g0074 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2848-1143C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229021 | ||||||
chr2:74229104
|
C | CTTTTTTT others(3): Show |
2 | a0001c0002t0001g0108a0003c0006t0001g0076 | 2 | HG02258.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2848-1236_2848-122 others(14): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229104 | ||||||
chr2:74229104
|
C | CTTTTTTT others(4): Show |
41 | a0001c0001t0001g0160a0001c0001t0003g0205a0001c0001t0008g0017others(38): Show | 41 | HG00558.hp2 HG00597.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.2848-1237_2848-122 others(15): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229104 | ||||||
chr2:74229104
|
C | CTTTTTTT others(5): Show |
138 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(135): Show | 139 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2848-1238_2848-122 others(16): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229104 | ||||||
chr2:74229104
|
C | CTTTTTTT others(6): Show |
15 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0200others(12): Show | 15 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2848-1227_2848-122 others(17): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229104 | ||||||
chr2:74229116
|
T | TTTTTTTT others(5): Show |
58 | a0001c0001t0001g0034a0001c0001t0002g0009a0001c0001t0002g0014others(55): Show | 58 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.2848-1239_2848-123 others(16): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229116 | ||||||
chr2:74229116
|
T | TTTTTTTT others(6): Show |
23 | a0001c0001t0001g0080a0001c0001t0002g0022a0001c0001t0002g0052others(20): Show | 23 | HG00597.hp2 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2848-1239_2848-123 others(17): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229116 | ||||||
chr2:74229116
|
T | TTTTTTTT others(7): Show |
2 | a0001c0001t0007g0159a0001c0001t0010g0278 | 2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2848-1239_2848-123 others(18): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229116 | ||||||
chr2:74229247
|
G | GT | 9 | a0001c0001t0001g0026a0001c0001t0001g0090a0001c0001t0001g0091others(6): Show | 9 | HG02055.hp1 HG03831.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.2848-1370dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229247 | ||||||
chr2:74229247
|
GT | G | 48 | a0001c0001t0001g0084a0001c0001t0004g0264a0001c0001t0018g0004others(45): Show | 48 | HG00558.hp2 HG00597.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.2848-1370delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229247 | ||||||
chr2:74229258
|
T | C | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2848-1380A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229258 | ||||||
chr2:74229258
|
T | TG | 3 | a0001c0001t0001g0093a0001c0003t0003g0274a0001c0003t0003g0276 | 3 | HG02572.hp1 HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2848-1381_2848-138 others(5): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229258 | ||||||
chr2:74229259
|
T | G | 64 | a0001c0001t0001g0084a0001c0001t0001g0093a0001c0001t0001g0095others(61): Show | 64 | HG00558.hp2 HG00597.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.2848-1381A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229259 | ||||||
chr2:74229259
|
T | TG | 35 | a0001c0001t0003g0203a0001c0001t0024g0141a0001c0003t0001g0028others(32): Show | 35 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.2848-1382dupC | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229259 | ||||||
chr2:74229263
|
G | C | 4 | a0002c0004t0004g0166a0002c0004t0004g0170a0002c0004t0004g0171others(1): Show | 4 | HG02615.hp1 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2848-1385C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229263 | ||||||
chr2:74229342
|
C | T | 1 | a0001c0001t0004g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2848-1464G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229342 | ||||||
chr2:74229550
|
C | G | 1 | a0001c0003t0003g0094 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2848-1672G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229550 | ||||||
chr2:74229777
|
G | A | 2 | a0001c0002t0001g0021a0001c0002t0001g0092 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2847+1459C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229777 | ||||||
chr2:74229849
|
G | A | 4 | a0001c0001t0010g0002a0001c0001t0010g0278a0001c0001t0010g0279others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2847+1387C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229849 | ||||||
chr2:74229881
|
G | GT | 91 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0034others(88): Show | 91 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.2847+1354dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229881 | ||||||
chr2:74229881
|
GT | G | 14 | a0001c0001t0001g0266a0001c0001t0004g0157a0001c0002t0001g0005others(11): Show | 14 | HG00741.hp1 HG01167.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.2847+1354delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229881 | ||||||
chr2:74229881
|
GTT | G | 27 | a0001c0002t0001g0046a0001c0002t0001g0065a0001c0002t0001g0066others(24): Show | 27 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.2847+1353_2847+135 others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229881 | ||||||
chr2:74229887
|
T | G | 38 | a0001c0001t0003g0203a0001c0001t0024g0141a0001c0003t0001g0028others(35): Show | 38 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.2847+1349A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229887 | ||||||
chr2:74229923
|
C | G | 1 | a0001c0002t0001g0207 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2847+1313G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74229923 | ||||||
chr2:74230180
|
G | C | 2 | a0001c0001t0018g0004a0001c0001t0020g0029 | 2 | HG00735.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2847+1056C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74230180 | ||||||
chr2:74230251
|
G | A | 4 | a0001c0001t0011g0103a0001c0001t0011g0162a0001c0001t0011g0190others(1): Show | 4 | HG01884.hp1 HG02257.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2847+985C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74230251 | ||||||
chr2:74230433
|
T | C | 8 | a0001c0001t0004g0264a0001c0001t0021g0261a0001c0002t0001g0021others(5): Show | 8 | HG02615.hp1 HG02630.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2847+803A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74230433 | ||||||
chr2:74230591
|
A | C | 129 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0093others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.2847+645T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74230591 | ||||||
chr2:74230661
|
T | A | 1 | a0001c0001t0020g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2847+575A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74230661 | ||||||
chr2:74230706
|
G | T | 3 | a0001c0001t0011g0103a0001c0001t0011g0162a0001c0001t0011g0190 | 3 | HG01884.hp1 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2847+530C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74230706 | ||||||
chr2:74230748
|
G | A | 4 | a0001c0001t0002g0056a0001c0001t0002g0057a0001c0001t0002g0058others(1): Show | 4 | HG02717.hp1 NA18949.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.2847+488C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74230748 | ||||||
chr2:74231003
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2847+233G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74231003 | ||||||
chr2:74231103
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0002g0251 | 2 | NA18942.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.2847+133C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74231103 | ||||||
chr2:74231106
|
C | T | 3 | a0001c0001t0003g0045a0001c0001t0003g0205a0001c0001t0003g0267 | 3 | HG01256.hp1 HG01258.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2847+130G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 25/30 | chr2 | 74231106 | ||||||
chr2:74231490
|
C | T | 1 | a0002c0004t0004g0170 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2775-182G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 24/30 | chr2 | 74231490 | ||||||
chr2:74231510
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2775-202A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 24/30 | chr2 | 74231510 | ||||||
chr2:74231516
|
A | C | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2775-208T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 24/30 | chr2 | 74231516 | ||||||
chr2:74231904
|
C | T | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2774+565G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 24/30 | chr2 | 74231904 | ||||||
chr2:74232104
|
G | A | 1 | a0001c0001t0004g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2774+365C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 24/30 | chr2 | 74232104 | ||||||
chr2:74232208
|
G | A | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2774+261C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 24/30 | chr2 | 74232208 | ||||||
chr2:74232335
|
T | C | 10 | a0001c0001t0007g0155a0001c0001t0007g0163a0001c0001t0009g0187others(7): Show | 10 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2774+134A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 24/30 | chr2 | 74232335 | ||||||
chr2:74232734
|
A | C | 1 | a0001c0001t0004g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2596-87T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 23/30 | chr2 | 74232734 | ||||||
chr2:74233072
|
G | A | 1 | a0001c0003t0005g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2595+330C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 23/30 | chr2 | 74233072 | ||||||
chr2:74233391
|
A | AC | 3 | a0001c0001t0006g0013a0003c0006t0001g0079a0004c0009t0007g0106 | 3 | HG02257.hp2 NA18939.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.2595+10dupG | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 23/30 | chr2 | 74233391 | ||||||
chr2:74233670
|
C | T | 1 | a0001c0001t0008g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2434-107G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74233670 | ||||||
chr2:74233777
|
A | G | 171 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0002g0009others(168): Show | 171 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.2434-214T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74233777 | ||||||
chr2:74233811
|
A | G | 1 | a0003c0005t0006g0281 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2434-248T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74233811 | ||||||
chr2:74233848
|
G | A | 1 | a0001c0003t0003g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2434-285C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74233848 | ||||||
chr2:74233902
|
G | C | 1 | a0001c0001t0002g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2434-339C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74233902 | ||||||
chr2:74234060
|
AAAAC | A | 54 | a0001c0001t0001g0034a0001c0001t0002g0009a0001c0001t0002g0014others(51): Show | 54 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.2434-501_2434-498d others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234060 | ||||||
chr2:74234082
|
C | CA | 44 | a0001c0002t0001g0005a0001c0002t0001g0021a0001c0002t0001g0046others(41): Show | 44 | HG00558.hp2 HG00597.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.2434-520dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234082 | ||||||
chr2:74234179
|
C | A | 1 | a0001c0003t0005g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2434-616G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234179 | ||||||
chr2:74234213
|
A | C | 172 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0002g0009others(169): Show | 172 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.2434-650T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234213 | ||||||
chr2:74234280
|
G | A | 1 | a0001c0001t0011g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2434-717C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234280 | ||||||
chr2:74234291
|
G | A | 9 | a0001c0002t0001g0122a0001c0002t0001g0123a0001c0002t0001g0151others(6): Show | 9 | HG01081.hp2 HG01109.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.2434-728C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234291 | ||||||
chr2:74234327
|
C | T | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2434-764G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234327 | ||||||
chr2:74234352
|
A | T | 1 | a0001c0001t0004g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2433+749T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234352 | ||||||
chr2:74234419
|
C | T | 4 | a0001c0001t0010g0002a0001c0001t0010g0278a0001c0001t0010g0279others(1): Show | 4 | HG02717.hp1 HG02896.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+682G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234419 | ||||||
chr2:74234428
|
C | T | 1 | a0002c0004t0003g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2433+673G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234428 | ||||||
chr2:74234507
|
G | A | 166 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0002g0009others(163): Show | 166 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.2433+594C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234507 | ||||||
chr2:74234810
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2433+291C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74234810 | ||||||
chr2:74235064
|
G | A | 1 | a0001c0001t0004g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2433+37C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 22/30 | chr2 | 74235064 | ||||||
chr2:74235364
|
T | C | 3 | a0001c0003t0003g0007a0001c0003t0003g0156a0001c0013t0003g0153 | 3 | HG01884.hp2 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2320-150A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74235364 | ||||||
chr2:74235514
|
T | G | 195 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(192): Show | 195 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.2320-300A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74235514 | ||||||
chr2:74235589
|
C | T | 1 | a0001c0001t0002g0145 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2320-375G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74235589 | ||||||
chr2:74235687
|
G | T | 1 | a0001c0001t0004g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2320-473C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74235687 | ||||||
chr2:74236439
|
C | T | 35 | a0001c0001t0024g0141a0001c0003t0001g0028a0001c0003t0001g0042others(32): Show | 35 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.2320-1225G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74236439 | ||||||
chr2:74236630
|
T | C | 2 | a0001c0002t0001g0257a0001c0002t0001g0259 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2320-1416A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74236630 | ||||||
chr2:74236977
|
A | AT | 123 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0002g0009others(120): Show | 123 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.2320-1764dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74236977 | ||||||
chr2:74236977
|
A | ATT | 42 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0001t0002g0014others(39): Show | 42 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.2320-1765_2320-176 others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74236977 | ||||||
chr2:74237038
|
G | A | 1 | a0002c0004t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2320-1824C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74237038 | ||||||
chr2:74237100
|
C | T | 2 | a0001c0002t0001g0046a0001c0002t0001g0185 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2320-1886G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74237100 | ||||||
chr2:74237447
|
G | T | 1 | a0001c0001t0004g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2319+1888C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74237447 | ||||||
chr2:74237622
|
A | G | 5 | a0001c0001t0007g0016a0001c0001t0007g0158a0001c0001t0007g0159others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319+1713T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74237622 | ||||||
chr2:74237632
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2319+1703C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74237632 | ||||||
chr2:74237678
|
C | T | 1 | a0001c0001t0027g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2319+1657G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74237678 | ||||||
chr2:74237715
|
C | T | 1 | a0001c0003t0003g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2319+1620G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74237715 | ||||||
chr2:74237757
|
T | C | 7 | a0001c0001t0007g0016a0001c0001t0007g0158a0001c0001t0007g0159others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2319+1578A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74237757 | ||||||
chr2:74237958
|
CG | C | 4 | a0001c0001t0007g0155a0002c0004t0007g0255a0002c0004t0014g0254others(1): Show | 4 | HG02451.hp1 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2319+1376delC | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74237958 | ||||||
chr2:74238027
|
G | A | 4 | a0001c0001t0007g0016a0001c0001t0007g0158a0001c0001t0007g0159others(1): Show | 4 | HG02145.hp1 HG02647.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319+1308C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74238027 | ||||||
chr2:74238638
|
G | A | 1 | a0001c0003t0017g0020 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2319+697C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74238638 | ||||||
chr2:74238778
|
C | T | 1 | a0003c0005t0001g0085 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2319+557G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74238778 | ||||||
chr2:74238989
|
A | C | 5 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0002g0024others(2): Show | 5 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(2): Show |
intron_variant | MODIFIER | c.2319+346T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74238989 | ||||||
chr2:74239025
|
T | C | 185 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(182): Show | 185 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.2319+310A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74239025 | ||||||
chr2:74239132
|
A | G | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2319+203T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74239132 | ||||||
chr2:74239172
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2319+163C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 21/30 | chr2 | 74239172 | ||||||
chr2:74239657
|
C | A | 1 | a0001c0003t0005g0181 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2119-122G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74239657 | ||||||
chr2:74239658
|
C | G | 2 | a0001c0001t0020g0029a0001c0014t0001g0265 | 2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2119-123G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74239658 | ||||||
chr2:74239678
|
C | T | 55 | a0001c0001t0001g0034a0001c0001t0002g0009a0001c0001t0002g0014others(52): Show | 55 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.2119-143G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74239678 | ||||||
chr2:74239767
|
A | G | 1 | a0001c0002t0001g0119 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2119-232T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74239767 | ||||||
chr2:74239795
|
T | TGCCTTTT others(10): Show |
183 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(180): Show | 183 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.2119-261_2119-260i others(19): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74239795 | ||||||
chr2:74239808
|
T | A | 5 | a0001c0001t0007g0016a0001c0001t0007g0158a0001c0001t0007g0159others(2): Show | 5 | HG02145.hp1 HG02647.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119-273A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74239808 | ||||||
chr2:74239814
|
A | C | 4 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(1): Show | 4 | NA18970.hp1 NA18981.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2119-279T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74239814 | ||||||
chr2:74239939
|
T | C | 4 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0068others(1): Show | 5 | NA18943.hp2 NA18970.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.2119-404A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74239939 | ||||||
chr2:74239958
|
T | TG | 34 | a0001c0001t0001g0165a0001c0001t0002g0116a0001c0001t0002g0121others(31): Show | 34 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.2119-424dupC | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74239958 | ||||||
chr2:74239995
|
C | T | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2119-460G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74239995 | ||||||
chr2:74240041
|
T | TTA | 24 | a0001c0001t0001g0033a0001c0001t0001g0198a0001c0001t0001g0216others(21): Show | 24 | HG00544.hp1 HG00621.hp2 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.2119-508_2119-507d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74240041 | ||||||
chr2:74240041
|
T | TTATATAT others(1): Show |
3 | a0001c0001t0011g0103a0001c0001t0011g0162a0001c0001t0011g0190 | 3 | HG01884.hp1 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2119-514_2119-507d others(10): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74240041 | ||||||
chr2:74240045
|
A | T | 1 | a0001c0003t0003g0206 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2119-510T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74240045 | ||||||
chr2:74240393
|
A | G | 1 | a0001c0003t0003g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2119-858T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74240393 | ||||||
chr2:74240509
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2119-974A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74240509 | ||||||
chr2:74240734
|
C | T | 6 | a0002c0004t0003g0168a0002c0004t0003g0169a0002c0004t0004g0166others(3): Show | 6 | HG02486.hp1 HG02615.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2119-1199G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74240734 | ||||||
chr2:74240748
|
T | C | 192 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(189): Show | 192 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.2119-1213A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74240748 | ||||||
chr2:74240769
|
C | CA | 105 | a0001c0001t0001g0093a0001c0001t0001g0160a0001c0001t0001g0165others(102): Show | 105 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.2118+1224dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74240769 | ||||||
chr2:74240769
|
C | CAA | 9 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0001t0007g0016others(6): Show | 9 | HG01192.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2118+1223_2118+122 others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74240769 | ||||||
chr2:74240886
|
C | T | 6 | a0002c0004t0003g0168a0002c0004t0003g0169a0002c0004t0004g0166others(3): Show | 6 | HG02486.hp1 HG02615.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2118+1108G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74240886 | ||||||
chr2:74241119
|
A | G | 194 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0080others(191): Show | 194 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.2118+875T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241119 | ||||||
chr2:74241193
|
G | A | 1 | a0001c0002t0001g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2118+801C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241193 | ||||||
chr2:74241249
|
A | ATAT | 86 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0036others(83): Show | 87 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.2118+742_2118+744d others(5): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241249 | ||||||
chr2:74241249
|
A | ATATTAT | 80 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0002g0009others(77): Show | 80 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.2118+739_2118+744d others(8): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241249 | ||||||
chr2:74241249
|
A | ATATTATT others(2): Show |
20 | a0001c0001t0001g0080a0001c0001t0002g0075a0001c0001t0002g0099others(17): Show | 20 | HG00673.hp2 HG00741.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.2118+736_2118+744d others(11): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241249 | ||||||
chr2:74241249
|
A | ATATTATT others(5): Show |
3 | a0001c0001t0007g0016a0001c0002t0001g0005a0002c0004t0003g0169 | 3 | HG01243.hp2 HG02486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2118+733_2118+744d others(14): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241249 | ||||||
chr2:74241249
|
A | ATATTATT others(8): Show |
7 | a0001c0001t0004g0157a0001c0001t0004g0264a0001c0001t0008g0096others(4): Show | 7 | HG02257.hp2 HG02896.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2118+730_2118+744d others(17): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241249 | ||||||
chr2:74241249
|
A | ATATTATT others(11): Show |
2 | a0001c0001t0008g0017a0001c0001t0008g0100 | 2 | HG02895.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2118+727_2118+744d others(20): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241249 | ||||||
chr2:74241257
|
A | ATTATTAT others(6): Show |
1 | a0001c0001t0008g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2118+724_2118+736d others(15): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241257 | ||||||
chr2:74241507
|
G | A | 1 | a0001c0003t0001g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2118+487C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241507 | ||||||
chr2:74241620
|
T | C | 1 | a0001c0002t0001g0065 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2118+374A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241620 | ||||||
chr2:74241683
|
G | A | 1 | a0001c0002t0002g0126 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2118+311C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241683 | ||||||
chr2:74241741
|
C | CA | 72 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0082others(69): Show | 72 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.2118+252dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241741 | ||||||
chr2:74241741
|
C | CAA | 8 | a0001c0001t0010g0279a0001c0003t0001g0042a0001c0003t0003g0012others(5): Show | 8 | HG01106.hp1 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2118+251_2118+252d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241741 | ||||||
chr2:74241763
|
A | C | 9 | a0001c0001t0004g0264a0001c0001t0021g0261a0002c0004t0003g0168others(6): Show | 9 | HG02486.hp1 HG02615.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2118+231T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241763 | ||||||
chr2:74241776
|
T | C | 5 | a0001c0001t0008g0017a0001c0001t0008g0096a0001c0001t0008g0100others(2): Show | 5 | HG02257.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2118+218A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 20/30 | chr2 | 74241776 | ||||||
chr2:74242092
|
G | A | 1 | a0001c0001t0004g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2060-40C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74242092 | ||||||
chr2:74242093
|
T | G | 2 | a0001c0001t0001g0235a0002c0004t0002g0210 | 2 | NA18973.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2060-41A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74242093 | ||||||
chr2:74242165
|
T | C | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2060-113A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74242165 | ||||||
chr2:74242275
|
C | T | 1 | a0002c0004t0001g0173 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2060-223G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74242275 | ||||||
chr2:74242609
|
T | C | 2 | a0001c0001t0011g0103a0001c0001t0011g0190 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2060-557A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74242609 | ||||||
chr2:74242652
|
C | T | 95 | a0001c0001t0001g0084a0001c0001t0001g0093a0001c0001t0001g0160others(92): Show | 95 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2060-600G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74242652 | ||||||
chr2:74242953
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2060-901G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74242953 | ||||||
chr2:74243007
|
G | A | 276 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(273): Show | 277 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(274): Show |
intron_variant | MODIFIER | c.2060-955C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74243007 | ||||||
chr2:74243121
|
T | G | 1 | a0001c0001t0002g0099 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2060-1069A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74243121 | ||||||
chr2:74243274
|
G | C | 6 | a0001c0001t0001g0084a0001c0001t0001g0093a0001c0001t0001g0160others(3): Show | 6 | HG02559.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2060-1222C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74243274 | ||||||
chr2:74243735
|
T | C | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2060-1683A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74243735 | ||||||
chr2:74243761
|
G | A | 2 | a0001c0001t0011g0103a0001c0001t0011g0190 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2060-1709C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74243761 | ||||||
chr2:74244002
|
G | C | 2 | a0001c0001t0011g0103a0001c0001t0011g0190 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2060-1950C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244002 | ||||||
chr2:74244029
|
G | A | 7 | a0001c0001t0001g0095a0001c0001t0008g0017a0001c0001t0008g0096others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2060-1977C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244029 | ||||||
chr2:74244247
|
C | T | 35 | a0001c0001t0001g0165a0001c0001t0002g0116a0001c0001t0002g0121others(32): Show | 35 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.2060-2195G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244247 | ||||||
chr2:74244352
|
G | C | 1 | a0001c0001t0025g0031 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2060-2300C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244352 | ||||||
chr2:74244374
|
G | A | 1 | a0003c0005t0001g0070 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2060-2322C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244374 | ||||||
chr2:74244405
|
C | G | 1 | a0001c0002t0001g0065 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2060-2353G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244405 | ||||||
chr2:74244444
|
T | C | 1 | a0001c0001t0002g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2060-2392A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244444 | ||||||
chr2:74244466
|
T | C | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2060-2414A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244466 | ||||||
chr2:74244468
|
C | CTCTT | 151 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(148): Show | 151 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.2060-2420_2060-241 others(8): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244468 | ||||||
chr2:74244468
|
C | T | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2060-2416G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244468 | ||||||
chr2:74244480
|
TC | T | 40 | a0001c0001t0008g0183a0001c0001t0019g0161a0001c0003t0001g0028others(37): Show | 40 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.2060-2429delG | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244480 | ||||||
chr2:74244484
|
C | T | 40 | a0001c0001t0008g0183a0001c0001t0019g0161a0001c0003t0001g0028others(37): Show | 40 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.2060-2432G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244484 | ||||||
chr2:74244486
|
T | C | 40 | a0001c0001t0008g0183a0001c0001t0019g0161a0001c0003t0001g0028others(37): Show | 40 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.2060-2434A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244486 | ||||||
chr2:74244488
|
CT | C | 40 | a0001c0001t0008g0183a0001c0001t0019g0161a0001c0003t0001g0028others(37): Show | 40 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.2060-2437delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244488 | ||||||
chr2:74244495
|
C | T | 40 | a0001c0001t0008g0183a0001c0001t0019g0161a0001c0003t0001g0028others(37): Show | 40 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.2060-2443G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244495 | ||||||
chr2:74244498
|
T | C | 40 | a0001c0001t0008g0183a0001c0001t0019g0161a0001c0003t0001g0028others(37): Show | 40 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.2060-2446A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244498 | ||||||
chr2:74244499
|
CCTT | C | 9 | a0001c0001t0015g0101a0001c0001t0015g0102a0001c0001t0019g0161others(6): Show | 9 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2060-2450_2060-244 others(7): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244499 | ||||||
chr2:74244572
|
T | A | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2059+2464A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74244572 | ||||||
chr2:74245059
|
C | T | 49 | a0001c0001t0001g0093a0001c0001t0001g0160a0001c0001t0008g0110others(46): Show | 49 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.2059+1977G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74245059 | ||||||
chr2:74245093
|
G | A | 2 | a0001c0002t0001g0257a0001c0002t0001g0259 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2059+1943C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74245093 | ||||||
chr2:74245152
|
G | A | 3 | a0001c0003t0003g0191a0001c0003t0003g0245a0001c0003t0003g0246 | 3 | HG02922.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2059+1884C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74245152 | ||||||
chr2:74245815
|
G | A | 50 | a0001c0001t0001g0034a0001c0001t0002g0009a0001c0001t0002g0014others(47): Show | 50 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.2059+1221C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74245815 | ||||||
chr2:74246190
|
C | T | 9 | a0001c0001t0004g0264a0001c0001t0021g0261a0002c0004t0003g0168others(6): Show | 9 | HG02486.hp1 HG02615.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2059+846G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74246190 | ||||||
chr2:74246227
|
A | G | 3 | a0001c0003t0003g0191a0001c0003t0003g0245a0001c0003t0003g0246 | 3 | HG02922.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2059+809T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74246227 | ||||||
chr2:74246439
|
G | A | 5 | a0001c0002t0001g0046a0001c0002t0001g0117a0001c0002t0001g0118others(2): Show | 5 | HG01070.hp2 HG01175.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2059+597C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74246439 | ||||||
chr2:74246491
|
A | G | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2059+545T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74246491 | ||||||
chr2:74246495
|
G | C | 9 | a0001c0001t0004g0264a0001c0001t0021g0261a0002c0004t0003g0168others(6): Show | 9 | HG02486.hp1 HG02615.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2059+541C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 19/30 | chr2 | 74246495 | ||||||
chr2:74247389
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1788-82G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247389 | ||||||
chr2:74247530
|
T | A | 1 | a0001c0001t0004g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1788-223A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247530 | ||||||
chr2:74247552
|
T | C | 21 | a0001c0001t0001g0217a0001c0001t0003g0193a0001c0003t0001g0028others(18): Show | 21 | HG00438.hp1 HG00544.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1788-245A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247552 | ||||||
chr2:74247566
|
C | G | 193 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(190): Show | 193 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.1788-259G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247566 | ||||||
chr2:74247659
|
C | A | 9 | a0001c0001t0004g0264a0001c0001t0021g0261a0002c0004t0003g0168others(6): Show | 9 | HG02486.hp1 HG02615.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1788-352G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247659 | ||||||
chr2:74247660
|
A | G | 4 | a0001c0001t0011g0103a0001c0001t0011g0190a0001c0001t0020g0029others(1): Show | 4 | HG01884.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1788-353T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247660 | ||||||
chr2:74247672
|
G | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0250a0001c0001t0001g0266 | 3 | HG01167.hp1 NA20752.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1788-365C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247672 | ||||||
chr2:74247705
|
G | T | 93 | a0001c0001t0001g0084a0001c0001t0001g0093a0001c0001t0001g0114others(90): Show | 93 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1788-398C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247705 | ||||||
chr2:74247824
|
T | A | 1 | a0001c0001t0002g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1788-517A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247824 | ||||||
chr2:74247827
|
T | C | 2 | a0001c0001t0002g0009a0001c0001t0002g0069 | 2 | HG02735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1788-520A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247827 | ||||||
chr2:74247880
|
A | AC | 7 | a0002c0004t0003g0168a0002c0004t0003g0169a0002c0004t0004g0166others(4): Show | 7 | HG02486.hp1 HG02615.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1787+472dupG | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247880 | ||||||
chr2:74247990
|
C | G | 1 | a0002c0004t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1787+363G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74247990 | ||||||
chr2:74248183
|
G | A | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1787+170C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74248183 | ||||||
chr2:74248232
|
T | A | 2 | a0001c0002t0001g0021a0001c0002t0001g0092 | 2 | HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1787+121A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74248232 | ||||||
chr2:74248307
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1787+46G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74248307 | ||||||
chr2:74248316
|
C | T | 5 | a0001c0001t0001g0093a0001c0001t0001g0160a0001c0001t0008g0110others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1787+37G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 18/30 | chr2 | 74248316 | ||||||
chr2:74248530
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1654-44G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74248530 | ||||||
chr2:74248578
|
G | A | 1 | a0001c0002t0001g0150 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1654-92C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74248578 | ||||||
chr2:74248669
|
T | C | 5 | a0001c0001t0001g0093a0001c0001t0001g0160a0001c0001t0008g0110others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1654-183A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74248669 | ||||||
chr2:74249061
|
T | C | 2 | a0001c0002t0001g0125a0001c0002t0001g0136 | 2 | NA18978.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1654-575A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74249061 | ||||||
chr2:74249159
|
T | C | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1654-673A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74249159 | ||||||
chr2:74249354
|
A | T | 1 | a0001c0002t0001g0066 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1654-868T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74249354 | ||||||
chr2:74249698
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1653+645T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74249698 | ||||||
chr2:74249714
|
C | T | 175 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(172): Show | 175 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.1653+629G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74249714 | ||||||
chr2:74249730
|
G | A | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1653+613C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74249730 | ||||||
chr2:74249934
|
C | A | 10 | a0001c0001t0001g0095a0001c0001t0008g0017a0001c0001t0008g0096others(7): Show | 10 | HG01192.hp1 HG01884.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1653+409G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74249934 | ||||||
chr2:74250060
|
G | A | 7 | a0001c0001t0001g0095a0001c0001t0008g0017a0001c0001t0008g0096others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1653+283C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74250060 | ||||||
chr2:74250300
|
G | A | 46 | a0001c0001t0001g0114a0001c0001t0001g0165a0001c0001t0002g0116others(43): Show | 46 | HG00558.hp2 HG00597.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.1653+43C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 17/30 | chr2 | 74250300 | ||||||
chr2:74250552
|
C | T | 1 | a0002c0004t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1479-35G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 16/30 | chr2 | 74250552 | ||||||
chr2:74250771
|
C | G | 1 | a0001c0001t0001g0025 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1479-254G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 16/30 | chr2 | 74250771 | ||||||
chr2:74250782
|
C | A | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1479-265G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 16/30 | chr2 | 74250782 | ||||||
chr2:74251311
|
T | G | 2 | a0001c0001t0002g0075a0001c0003t0005g0177 | 2 | HG00673.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1479-794A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 16/30 | chr2 | 74251311 | ||||||
chr2:74251448
|
A | G | 1 | a0001c0001t0026g0107 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1478+731T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 16/30 | chr2 | 74251448 | ||||||
chr2:74251469
|
T | TA | 7 | a0001c0001t0001g0095a0001c0001t0008g0017a0001c0001t0008g0096others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1478+709dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 16/30 | chr2 | 74251469 | ||||||
chr2:74251707
|
C | T | 45 | a0001c0001t0001g0114a0001c0001t0001g0165a0001c0001t0002g0116others(42): Show | 45 | HG00558.hp2 HG00597.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1478+472G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 16/30 | chr2 | 74251707 | ||||||
chr2:74251798
|
T | C | 3 | a0001c0001t0015g0101a0001c0001t0015g0102a0001c0001t0021g0261 | 3 | HG02451.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1478+381A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 16/30 | chr2 | 74251798 | ||||||
chr2:74252076
|
G | A | 1 | a0001c0002t0001g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1478+103C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 16/30 | chr2 | 74252076 | ||||||
chr2:74252877
|
T | C | 2 | a0001c0001t0020g0029a0001c0014t0001g0265 | 2 | HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1268+97A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 15/30 | chr2 | 74252877 | ||||||
chr2:74253196
|
C | A | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1114-68G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253196 | ||||||
chr2:74253253
|
A | C | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1114-125T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253253 | ||||||
chr2:74253392
|
A | G | 1 | a0001c0001t0004g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1114-264T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253392 | ||||||
chr2:74253475
|
T | C | 192 | a0001c0001t0001g0034a0001c0001t0001g0080a0001c0001t0001g0084others(189): Show | 192 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.1114-347A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253475 | ||||||
chr2:74253518
|
C | T | 2 | a0001c0001t0004g0157a0001c0001t0019g0161 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1114-390G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253518 | ||||||
chr2:74253519
|
C | T | 13 | a0001c0003t0001g0233a0001c0003t0003g0012a0001c0003t0003g0081others(10): Show | 13 | HG00280.hp2 HG01106.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1114-391G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253519 | ||||||
chr2:74253532
|
C | T | 55 | a0001c0001t0001g0034a0001c0001t0002g0009a0001c0001t0002g0014others(52): Show | 55 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1114-404G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253532 | ||||||
chr2:74253655
|
A | G | 7 | a0001c0001t0001g0095a0001c0001t0008g0017a0001c0001t0008g0096others(4): Show | 7 | HG01192.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1114-527T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253655 | ||||||
chr2:74253665
|
T | C | 3 | a0001c0002t0001g0021a0001c0002t0001g0092a0001c0007t0004g0006 | 3 | HG02630.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1114-537A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253665 | ||||||
chr2:74253715
|
A | T | 9 | a0001c0001t0001g0114a0001c0002t0001g0083a0001c0002t0001g0111others(6): Show | 9 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1114-587T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253715 | ||||||
chr2:74253841
|
GT | G | 6 | a0001c0001t0001g0095a0001c0001t0008g0017a0001c0001t0008g0096others(3): Show | 6 | HG01192.hp1 HG02257.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114-714delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74253841 | ||||||
chr2:74254096
|
C | T | 60 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0220others(57): Show | 60 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1113+523G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74254096 | ||||||
chr2:74254178
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1113+441C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74254178 | ||||||
chr2:74254202
|
T | C | 5 | a0001c0001t0007g0158a0001c0001t0007g0159a0001c0001t0008g0183others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1113+417A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 14/30 | chr2 | 74254202 | ||||||
chr2:74254817
|
A | AT | 85 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0165others(82): Show | 85 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1026-112dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74254817 | ||||||
chr2:74254850
|
C | T | 2 | a0001c0001t0008g0258a0001c0001t0008g0263 | 2 | HG01109.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1026-144G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74254850 | ||||||
chr2:74254880
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1026-174G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74254880 | ||||||
chr2:74255012
|
G | A | 3 | a0001c0003t0003g0191a0001c0003t0003g0245a0001c0003t0003g0246 | 3 | HG02922.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1026-306C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74255012 | ||||||
chr2:74255112
|
C | T | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1026-406G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74255112 | ||||||
chr2:74255246
|
T | G | 1 | a0002c0010t0004g0105 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1025+529A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74255246 | ||||||
chr2:74255362
|
G | A | 3 | a0002c0004t0007g0255a0002c0004t0014g0254a0002c0004t0014g0256 | 3 | HG02622.hp2 HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1025+413C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74255362 | ||||||
chr2:74255421
|
G | T | 89 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(86): Show | 89 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.1025+354C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74255421 | ||||||
chr2:74255440
|
G | C | 1 | a0001c0007t0004g0006 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1025+335C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74255440 | ||||||
chr2:74255477
|
T | C | 3 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0243 | 3 | HG01175.hp2 HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1025+298A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74255477 | ||||||
chr2:74255765
|
T | C | 83 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(80): Show | 83 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1025+10A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 13/30 | chr2 | 74255765 | ||||||
chr2:74256063
|
A | T | 8 | a0001c0001t0002g0115a0001c0001t0003g0260a0001c0001t0004g0264others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.868-131T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74256063 | ||||||
chr2:74256375
|
G | C | 3 | a0001c0001t0003g0260a0001c0002t0001g0257a0001c0002t0001g0259 | 3 | HG01167.hp2 HG01169.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.868-443C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74256375 | ||||||
chr2:74256561
|
G | A | 60 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.868-629C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74256561 | ||||||
chr2:74256601
|
C | T | 3 | a0001c0001t0007g0155a0001c0003t0003g0156a0001c0013t0003g0153 | 3 | HG01884.hp2 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.868-669G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74256601 | ||||||
chr2:74256875
|
A | G | 5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.868-943T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74256875 | ||||||
chr2:74257000
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.868-1068C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257000 | ||||||
chr2:74257001
|
C | T | 1 | a0001c0003t0005g0178 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.868-1069G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257001 | ||||||
chr2:74257079
|
G | A | 1 | a0001c0001t0001g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.868-1147C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257079 | ||||||
chr2:74257096
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.868-1164C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257096 | ||||||
chr2:74257203
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.868-1271C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257203 | ||||||
chr2:74257247
|
C | CA | 61 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(58): Show | 61 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.868-1316dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257247 | ||||||
chr2:74257405
|
G | A | 1 | a0001c0014t0001g0265 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.868-1473C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257405 | ||||||
chr2:74257445
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.868-1513G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257445 | ||||||
chr2:74257471
|
G | T | 2 | a0001c0001t0007g0163a0001c0001t0018g0004 | 2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.868-1539C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257471 | ||||||
chr2:74257689
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.868-1757G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257689 | ||||||
chr2:74257812
|
A | G | 173 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(170): Show | 173 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.867+1776T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257812 | ||||||
chr2:74257818
|
T | C | 1 | a0001c0001t0002g0275 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.867+1770A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74257818 | ||||||
chr2:74258267
|
C | T | 1 | a0003c0005t0002g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.867+1321G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74258267 | ||||||
chr2:74258570
|
G | A | 172 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(169): Show | 172 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.867+1018C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74258570 | ||||||
chr2:74258769
|
T | G | 54 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(51): Show | 54 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.867+819A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74258769 | ||||||
chr2:74258897
|
G | T | 1 | a0003c0005t0001g0227 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.867+691C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74258897 | ||||||
chr2:74259067
|
C | G | 3 | a0001c0001t0002g0069a0001c0003t0003g0081a0001c0003t0003g0215 | 3 | HG01123.hp2 HG02735.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.867+521G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74259067 | ||||||
chr2:74259082
|
A | G | 2 | a0001c0001t0015g0101a0001c0001t0015g0102 | 2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.867+506T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74259082 | ||||||
chr2:74259111
|
C | T | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.867+477G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74259111 | ||||||
chr2:74259112
|
G | A | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.867+476C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74259112 | ||||||
chr2:74259191
|
G | A | 1 | a0001c0001t0010g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.867+397C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74259191 | ||||||
chr2:74259230
|
G | A | 172 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(169): Show | 172 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.867+358C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74259230 | ||||||
chr2:74259267
|
G | T | 3 | a0001c0001t0007g0155a0001c0003t0003g0156a0001c0013t0003g0153 | 3 | HG01884.hp2 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.867+321C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74259267 | ||||||
chr2:74259423
|
T | A | 64 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.867+165A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74259423 | ||||||
chr2:74259578
|
G | A | 1 | a0001c0003t0003g0234 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.867+10C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 12/30 | chr2 | 74259578 | ||||||
chr2:74259742
|
C | A | 19 | a0001c0001t0002g0115a0001c0001t0004g0264a0001c0001t0008g0100others(16): Show | 19 | HG00621.hp2 HG01884.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.812-99G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74259742 | ||||||
chr2:74259942
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.812-299C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74259942 | ||||||
chr2:74260029
|
G | T | 3 | a0001c0001t0001g0220a0001c0001t0001g0248a0001c0001t0006g0247 | 3 | NA18941.hp1 NA19002.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.812-386C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74260029 | ||||||
chr2:74260086
|
T | C | 4 | a0001c0001t0003g0260a0001c0001t0021g0261a0001c0002t0001g0257others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.812-443A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74260086 | ||||||
chr2:74260165
|
C | G | 3 | a0001c0001t0001g0138a0001c0003t0003g0078a0001c0003t0003g0280 | 3 | HG00408.hp2 HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.812-522G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74260165 | ||||||
chr2:74260169
|
T | C | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.812-526A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74260169 | ||||||
chr2:74260226
|
C | G | 1 | a0002c0004t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.812-583G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74260226 | ||||||
chr2:74260236
|
C | A | 1 | a0001c0001t0016g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.812-593G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74260236 | ||||||
chr2:74260236
|
C | T | 2 | a0002c0010t0004g0105a0004c0009t0007g0106 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.812-593G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74260236 | ||||||
chr2:74260361
|
C | T | 1 | a0001c0003t0001g0028 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.812-718G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74260361 | ||||||
chr2:74260596
|
C | T | 1 | a0002c0004t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.812-953G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74260596 | ||||||
chr2:74260742
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.812-1099T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74260742 | ||||||
chr2:74261005
|
C | G | 9 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(6): Show | 9 | HG01243.hp2 HG02280.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.811+1132G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261005 | ||||||
chr2:74261032
|
A | C | 54 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(51): Show | 54 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.811+1105T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261032 | ||||||
chr2:74261092
|
C | T | 68 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(65): Show | 68 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.811+1045G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261092 | ||||||
chr2:74261325
|
A | G | 176 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(173): Show | 176 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.811+812T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261325 | ||||||
chr2:74261441
|
G | T | 3 | a0001c0001t0013g0018a0001c0001t0013g0019a0001c0003t0017g0020 | 3 | HG00597.hp2 NA18747.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.811+696C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261441 | ||||||
chr2:74261457
|
A | G | 5 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(2): Show | 5 | HG02280.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.811+680T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261457 | ||||||
chr2:74261571
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(265): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.811+566A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261571 | ||||||
chr2:74261625
|
T | C | 1 | a0001c0002t0001g0207 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.811+512A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261625 | ||||||
chr2:74261686
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.811+451C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261686 | ||||||
chr2:74261717
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.811+420C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261717 | ||||||
chr2:74261810
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.811+327A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261810 | ||||||
chr2:74261882
|
T | C | 21 | a0002c0004t0001g0104a0002c0004t0001g0173a0002c0004t0001g0202others(18): Show | 21 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.811+255A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261882 | ||||||
chr2:74261935
|
G | A | 21 | a0002c0004t0001g0104a0002c0004t0001g0173a0002c0004t0001g0202others(18): Show | 21 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.811+202C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74261935 | ||||||
chr2:74262073
|
T | C | 7 | a0001c0001t0001g0114a0001c0001t0004g0157a0001c0001t0008g0110others(4): Show | 7 | HG00741.hp1 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.811+64A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 11/30 | chr2 | 74262073 | ||||||
chr2:74262361
|
T | C | 9 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(6): Show | 9 | HG01243.hp2 HG02280.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.716-129A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74262361 | ||||||
chr2:74262363
|
C | CT | 32 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064others(29): Show | 32 | HG00621.hp2 HG01169.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.716-132dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74262363 | ||||||
chr2:74262363
|
CT | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0228a0001c0001t0001g0232others(4): Show | 7 | HG01256.hp2 HG01975.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.716-132delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74262363 | ||||||
chr2:74262382
|
T | A | 1 | a0001c0001t0002g0139 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.716-150A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74262382 | ||||||
chr2:74262438
|
G | A | 64 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.716-206C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74262438 | ||||||
chr2:74262623
|
C | T | 21 | a0002c0004t0001g0104a0002c0004t0001g0173a0002c0004t0001g0202others(18): Show | 21 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.716-391G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74262623 | ||||||
chr2:74262690
|
C | T | 64 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.716-458G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74262690 | ||||||
chr2:74262705
|
A | G | 9 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(6): Show | 9 | HG01243.hp2 HG02280.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.716-473T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74262705 | ||||||
chr2:74262913
|
C | T | 3 | a0001c0001t0001g0080a0001c0001t0008g0258a0001c0001t0008g0263 | 3 | HG01109.hp1 HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.716-681G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74262913 | ||||||
chr2:74263036
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0003g0218 | 2 | NA18948.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.716-804C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74263036 | ||||||
chr2:74263096
|
A | G | 49 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(46): Show | 49 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.716-864T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74263096 | ||||||
chr2:74263102
|
C | T | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.716-870G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74263102 | ||||||
chr2:74263375
|
C | T | 66 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(63): Show | 66 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.715+772G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74263375 | ||||||
chr2:74263774
|
T | C | 1 | a0003c0006t0001g0076 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.715+373A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74263774 | ||||||
chr2:74264116
|
C | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0036a0006c0011t0001g0035 | 4 | NA18943.hp2 NA18970.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+31G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 10/30 | chr2 | 74264116 | ||||||
chr2:74264486
|
G | T | 1 | a0001c0002t0001g0143 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.563-187C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264486 | ||||||
chr2:74264489
|
C | CGT | 21 | a0001c0001t0001g0216a0001c0001t0010g0278a0001c0001t0010g0279others(18): Show | 21 | HG01257.hp2 HG01258.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.563-192_563-191dup others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264489 | ||||||
chr2:74264489
|
C | CGTGT | 8 | a0001c0001t0001g0093a0001c0001t0001g0200a0001c0001t0001g0250others(5): Show | 8 | HG00673.hp1 HG01167.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.563-194_563-191dup others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264489 | ||||||
chr2:74264489
|
C | CGTGTGT | 7 | a0001c0001t0001g0114a0001c0001t0002g0115a0001c0001t0011g0103others(4): Show | 7 | HG01884.hp1 HG02922.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.563-196_563-191dup others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264489 | ||||||
chr2:74264489
|
C | CGTGTGTG others(1): Show |
10 | a0001c0001t0004g0157a0001c0001t0009g0187a0001c0001t0009g0189others(7): Show | 10 | HG00741.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.563-198_563-191dup others(8): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264489 | ||||||
chr2:74264489
|
C | CGTGTGTG others(3): Show |
32 | a0001c0001t0001g0095a0001c0001t0002g0062a0001c0001t0002g0063others(29): Show | 32 | HG00621.hp2 HG00735.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.563-200_563-191dup others(10): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264489 | ||||||
chr2:74264489
|
C | CGTGTGTG others(5): Show |
20 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0086others(17): Show | 20 | HG01081.hp2 HG01109.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.563-202_563-191dup others(12): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264489 | ||||||
chr2:74264489
|
C | CGTGTGTG others(7): Show |
49 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0223others(46): Show | 49 | HG00558.hp2 HG00597.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.563-204_563-191dup others(14): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264489 | ||||||
chr2:74264489
|
C | CGTGTGTG others(9): Show |
23 | a0001c0001t0001g0034a0001c0001t0001g0068a0001c0001t0001g0109others(20): Show | 23 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.563-206_563-191dup others(16): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264489 | ||||||
chr2:74264489
|
C | CGTGTGTG others(11): Show |
12 | a0001c0001t0001g0033a0001c0001t0001g0138a0001c0001t0001g0269others(9): Show | 12 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.563-208_563-191dup others(18): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264489 | ||||||
chr2:74264489
|
C | CGTGTGTG others(13): Show |
11 | a0001c0001t0001g0084a0001c0001t0001g0268a0001c0001t0002g0009others(8): Show | 11 | HG00280.hp1 HG00408.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.563-210_563-191dup others(20): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264489 | ||||||
chr2:74264562
|
C | G | 1 | a0002c0004t0001g0271 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.563-263G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264562 | ||||||
chr2:74264716
|
T | C | 1 | a0001c0003t0003g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.562+388A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264716 | ||||||
chr2:74264771
|
A | C | 65 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(62): Show | 65 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.562+333T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264771 | ||||||
chr2:74264994
|
G | C | 10 | a0002c0004t0001g0173a0002c0004t0003g0168a0002c0004t0003g0169others(7): Show | 10 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.562+110C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74264994 | ||||||
chr2:74265026
|
G | A | 5 | a0001c0001t0001g0093a0001c0001t0007g0016a0001c0001t0011g0162others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.562+78C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 9/30 | chr2 | 74265026 | ||||||
chr2:74265401
|
G | A | 1 | a0001c0003t0005g0180 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.402-137C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74265401 | ||||||
chr2:74265516
|
G | T | 49 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(46): Show | 49 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.402-252C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74265516 | ||||||
chr2:74265957
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.402-693G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74265957 | ||||||
chr2:74266354
|
G | A | 1 | a0007c0015t0001g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.402-1090C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74266354 | ||||||
chr2:74266805
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.402-1541T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74266805 | ||||||
chr2:74266864
|
T | C | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.402-1600A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74266864 | ||||||
chr2:74267068
|
C | T | 2 | a0001c0002t0001g0098a0001c0002t0002g0126 | 2 | HG02132.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.402-1804G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74267068 | ||||||
chr2:74267142
|
A | G | 4 | a0001c0001t0003g0260a0001c0001t0021g0261a0001c0002t0001g0257others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-1878T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74267142 | ||||||
chr2:74267409
|
T | C | 2 | a0001c0001t0007g0163a0001c0001t0018g0004 | 2 | HG00735.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.402-2145A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74267409 | ||||||
chr2:74267505
|
C | T | 12 | a0001c0001t0001g0138a0001c0001t0002g0174a0001c0001t0002g0176others(9): Show | 12 | HG00408.hp2 HG00438.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.402-2241G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74267505 | ||||||
chr2:74267524
|
T | C | 3 | a0001c0001t0002g0275a0001c0003t0003g0274a0001c0003t0003g0276 | 3 | HG02572.hp1 HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.402-2260A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74267524 | ||||||
chr2:74267653
|
C | A | 1 | a0002c0004t0001g0173 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.402-2389G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74267653 | ||||||
chr2:74267885
|
C | G | 4 | a0001c0001t0003g0260a0001c0001t0021g0261a0001c0002t0001g0257others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-2621G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74267885 | ||||||
chr2:74267986
|
AT | A | 8 | a0001c0001t0001g0086a0001c0001t0001g0232a0001c0001t0002g0009others(5): Show | 8 | HG02523.hp1 HG03098.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.402-2723delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74267986 | ||||||
chr2:74268286
|
G | A | 34 | a0001c0001t0003g0260a0001c0001t0009g0187a0001c0001t0009g0189others(31): Show | 34 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.402-3022C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268286 | ||||||
chr2:74268405
|
G | T | 1 | a0003c0005t0006g0087 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.402-3141C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268405 | ||||||
chr2:74268547
|
C | G | 1 | a0001c0001t0001g0023 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.402-3283G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268547 | ||||||
chr2:74268604
|
T | A | 4 | a0001c0001t0003g0260a0001c0001t0021g0261a0001c0002t0001g0257others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-3340A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268604 | ||||||
chr2:74268787
|
G | A | 170 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(167): Show | 170 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.402-3523C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268787 | ||||||
chr2:74268833
|
T | C | 13 | a0002c0004t0001g0173a0002c0004t0003g0168a0002c0004t0003g0169others(10): Show | 13 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.402-3569A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268833 | ||||||
chr2:74268914
|
T | C | 2 | a0002c0010t0004g0105a0004c0009t0007g0106 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.402-3650A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268914 | ||||||
chr2:74268916
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.402-3652G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268916 | ||||||
chr2:74268929
|
C | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(1): Show | 4 | HG01192.hp1 HG02896.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.402-3665G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268929 | ||||||
chr2:74268937
|
C | T | 1 | a0001c0001t0003g0194 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.402-3673G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268937 | ||||||
chr2:74268942
|
C | G | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.402-3678G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74268942 | ||||||
chr2:74269211
|
T | A | 3 | a0001c0001t0013g0018a0001c0001t0013g0019a0001c0003t0017g0020 | 3 | HG00597.hp2 NA18747.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.402-3947A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74269211 | ||||||
chr2:74269228
|
C | T | 8 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(5): Show | 8 | HG02280.hp1 HG02976.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.402-3964G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74269228 | ||||||
chr2:74269372
|
TTTG | T | 63 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.402-4111_402-4109d others(5): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74269372 | ||||||
chr2:74269378
|
T | TTTTG | 60 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.402-4118_402-4115d others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74269378 | ||||||
chr2:74269378
|
T | TTTTGTTT others(1): Show |
3 | a0001c0001t0001g0109a0001c0003t0003g0012a0003c0005t0006g0281 | 3 | HG00621.hp2 HG01106.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.402-4122_402-4115d others(10): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74269378 | ||||||
chr2:74269378
|
TTTTG | T | 6 | a0001c0001t0001g0198a0001c0001t0009g0187a0001c0001t0009g0189others(3): Show | 6 | HG02280.hp1 HG02976.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.402-4118_402-4115d others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74269378 | ||||||
chr2:74269382
|
G | T | 2 | a0001c0001t0004g0264a0002c0004t0001g0104 | 2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.402-4118C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74269382 | ||||||
chr2:74269524
|
C | T | 8 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(5): Show | 8 | HG02280.hp1 HG02976.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.402-4260G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74269524 | ||||||
chr2:74269529
|
G | A | 3 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0001t0016g0003 | 3 | HG03098.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.402-4265C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74269529 | ||||||
chr2:74269727
|
G | A | 21 | a0002c0004t0001g0104a0002c0004t0001g0173a0002c0004t0001g0202others(18): Show | 21 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.402-4463C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74269727 | ||||||
chr2:74270165
|
C | T | 3 | a0001c0001t0002g0069a0001c0003t0003g0081a0001c0003t0003g0215 | 3 | HG01123.hp2 HG02735.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.402-4901G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74270165 | ||||||
chr2:74270179
|
C | T | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.402-4915G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74270179 | ||||||
chr2:74270326
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(272): Show | 276 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.402-5062T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74270326 | ||||||
chr2:74270401
|
C | T | 21 | a0002c0004t0001g0104a0002c0004t0001g0173a0002c0004t0001g0202others(18): Show | 21 | HG02055.hp1 HG02257.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.402-5137G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74270401 | ||||||
chr2:74270500
|
T | C | 1 | a0001c0001t0025g0031 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.402-5236A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74270500 | ||||||
chr2:74270752
|
G | A | 1 | a0001c0001t0019g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.402-5488C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74270752 | ||||||
chr2:74270979
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.402-5715C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74270979 | ||||||
chr2:74271525
|
C | T | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.402-6261G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74271525 | ||||||
chr2:74271568
|
A | C | 1 | a0001c0001t0001g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.402-6304T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74271568 | ||||||
chr2:74271745
|
G | T | 4 | a0001c0001t0003g0260a0001c0001t0021g0261a0001c0002t0001g0257others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-6481C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74271745 | ||||||
chr2:74271782
|
T | C | 190 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(187): Show | 190 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.402-6518A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74271782 | ||||||
chr2:74271825
|
T | A | 1 | a0001c0001t0008g0100 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.402-6561A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74271825 | ||||||
chr2:74271826
|
G | A | 1 | a0001c0001t0003g0218 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.402-6562C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74271826 | ||||||
chr2:74272012
|
G | C | 2 | a0002c0010t0004g0105a0004c0009t0007g0106 | 2 | HG02257.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.402-6748C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74272012 | ||||||
chr2:74272053
|
G | T | 172 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(169): Show | 172 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.402-6789C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74272053 | ||||||
chr2:74272634
|
G | A | 1 | a0002c0004t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.402-7370C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74272634 | ||||||
chr2:74273167
|
C | G | 1 | a0001c0001t0002g0067 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.402-7903G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74273167 | ||||||
chr2:74273213
|
C | T | 1 | a0001c0001t0006g0127 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.402-7949G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74273213 | ||||||
chr2:74273346
|
T | C | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.402-8082A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74273346 | ||||||
chr2:74273467
|
C | T | 1 | a0001c0001t0011g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.402-8203G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74273467 | ||||||
chr2:74273732
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.402-8468A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74273732 | ||||||
chr2:74273827
|
G | C | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.402-8563C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74273827 | ||||||
chr2:74273870
|
G | A | 5 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(2): Show | 5 | HG02280.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.402-8606C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74273870 | ||||||
chr2:74273981
|
A | G | 64 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.402-8717T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74273981 | ||||||
chr2:74273998
|
G | C | 171 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(168): Show | 171 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.402-8734C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74273998 | ||||||
chr2:74274211
|
G | A | 2 | a0001c0002t0001g0129a0001c0002t0001g0137 | 2 | NA18973.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.402-8947C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74274211 | ||||||
chr2:74274382
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.402-9118G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74274382 | ||||||
chr2:74274383
|
A | G | 58 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(55): Show | 58 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.402-9119T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74274383 | ||||||
chr2:74274410
|
TACA | T | 67 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(64): Show | 67 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.402-9149_402-9147d others(5): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74274410 | ||||||
chr2:74274654
|
T | C | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.402-9390A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74274654 | ||||||
chr2:74274697
|
T | G | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.402-9433A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74274697 | ||||||
chr2:74274712
|
A | G | 1 | a0001c0001t0011g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.402-9448T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74274712 | ||||||
chr2:74274817
|
C | A | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.402-9553G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74274817 | ||||||
chr2:74274817
|
C | T | 170 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(167): Show | 170 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.402-9553G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74274817 | ||||||
chr2:74274918
|
G | A | 1 | a0001c0001t0020g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.402-9654C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74274918 | ||||||
chr2:74275161
|
G | A | 1 | a0003c0006t0001g0076 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.402-9897C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74275161 | ||||||
chr2:74275264
|
G | C | 9 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0026others(6): Show | 10 | HG00438.hp2 HG02155.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.402-10000C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74275264 | ||||||
chr2:74275268
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.402-10004G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74275268 | ||||||
chr2:74275363
|
G | T | 3 | a0001c0001t0003g0260a0001c0002t0001g0257a0001c0002t0001g0259 | 3 | HG01167.hp2 HG01169.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.402-10099C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74275363 | ||||||
chr2:74275371
|
A | C | 1 | a0001c0001t0002g0251 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.402-10107T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74275371 | ||||||
chr2:74275390
|
C | A | 4 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.402-10126G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74275390 | ||||||
chr2:74275589
|
TCCTTCCC others(16): Show |
T | 5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.401+10161_401+1018 others(27): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74275589 | ||||||
chr2:74275885
|
C | T | 171 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(168): Show | 171 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.401+9888G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74275885 | ||||||
chr2:74276063
|
T | C | 70 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(67): Show | 70 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.401+9710A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74276063 | ||||||
chr2:74276083
|
G | T | 63 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.401+9690C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74276083 | ||||||
chr2:74276668
|
C | CTTCATTA others(20): Show |
166 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(163): Show | 166 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.401+9078_401+9104d others(29): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74276668 | ||||||
chr2:74276668
|
C | CTTCATTA others(47): Show |
5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.401+9104_401+9105i others(56): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74276668 | ||||||
chr2:74276716
|
T | C | 4 | a0001c0001t0003g0260a0001c0001t0021g0261a0001c0002t0001g0257others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.401+9057A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74276716 | ||||||
chr2:74276717
|
G | A | 4 | a0001c0001t0003g0260a0001c0001t0021g0261a0001c0002t0001g0257others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.401+9056C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74276717 | ||||||
chr2:74276740
|
T | A | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.401+9033A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74276740 | ||||||
chr2:74276845
|
G | A | 1 | a0001c0003t0003g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.401+8928C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74276845 | ||||||
chr2:74276864
|
A | T | 1 | a0002c0004t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.401+8909T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74276864 | ||||||
chr2:74276956
|
G | C | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.401+8817C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74276956 | ||||||
chr2:74277038
|
G | T | 1 | a0001c0001t0011g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.401+8735C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74277038 | ||||||
chr2:74277045
|
A | G | 2 | a0001c0001t0007g0158a0001c0001t0007g0159 | 2 | HG02145.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.401+8728T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74277045 | ||||||
chr2:74277306
|
T | G | 1 | a0001c0001t0002g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.401+8467A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74277306 | ||||||
chr2:74277442
|
G | A | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0064 | 3 | NA18970.hp1 NA18981.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.401+8331C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74277442 | ||||||
chr2:74277782
|
G | A | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.401+7991C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74277782 | ||||||
chr2:74277818
|
C | T | 1 | a0001c0001t0011g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.401+7955G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74277818 | ||||||
chr2:74277918
|
C | CA | 9 | a0001c0001t0001g0114a0001c0001t0004g0157a0001c0001t0007g0163others(6): Show | 9 | HG00735.hp1 HG00741.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.401+7854dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74277918 | ||||||
chr2:74277921
|
A | C | 2 | a0001c0001t0022g0197a0005c0012t0002g0041 | 2 | HG00544.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.401+7852T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74277921 | ||||||
chr2:74277971
|
T | C | 1 | a0001c0001t0011g0162 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.401+7802A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74277971 | ||||||
chr2:74278952
|
C | T | 1 | a0002c0004t0002g0210 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.401+6821G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74278952 | ||||||
chr2:74278964
|
C | G | 171 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(168): Show | 171 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.401+6809G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74278964 | ||||||
chr2:74278978
|
A | G | 4 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(1): Show | 4 | HG01192.hp1 HG02896.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.401+6795T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74278978 | ||||||
chr2:74279107
|
C | T | 2 | a0001c0001t0002g0133a0001c0001t0006g0127 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.401+6666G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74279107 | ||||||
chr2:74279327
|
C | T | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.401+6446G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74279327 | ||||||
chr2:74279328
|
G | A | 1 | a0001c0001t0019g0161 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.401+6445C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74279328 | ||||||
chr2:74279514
|
C | T | 3 | a0001c0001t0003g0260a0001c0002t0001g0257a0001c0002t0001g0259 | 3 | HG01167.hp2 HG01169.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.401+6259G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74279514 | ||||||
chr2:74279632
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.401+6141G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74279632 | ||||||
chr2:74279823
|
T | C | 4 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0243others(1): Show | 4 | HG01175.hp2 HG01928.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.401+5950A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74279823 | ||||||
chr2:74279849
|
C | T | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.401+5924G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74279849 | ||||||
chr2:74280082
|
C | G | 5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.401+5691G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280082 | ||||||
chr2:74280236
|
T | C | 5 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(2): Show | 5 | HG02280.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.401+5537A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280236 | ||||||
chr2:74280240
|
T | C | 5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.401+5533A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280240 | ||||||
chr2:74280340
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.401+5433G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280340 | ||||||
chr2:74280421
|
G | C | 2 | a0001c0003t0003g0245a0001c0003t0003g0246 | 2 | HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.401+5352C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280421 | ||||||
chr2:74280445
|
G | A | 64 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.401+5328C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280445 | ||||||
chr2:74280685
|
AT | A | 154 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(151): Show | 154 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.401+5087delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280685 | ||||||
chr2:74280753
|
C | T | 171 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(168): Show | 171 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.401+5020G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280753 | ||||||
chr2:74280766
|
C | G | 1 | a0002c0004t0007g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.401+5007G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280766 | ||||||
chr2:74280772
|
C | G | 1 | a0001c0001t0002g0022 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.401+5001G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280772 | ||||||
chr2:74280820
|
T | G | 171 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(168): Show | 171 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.401+4953A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74280820 | ||||||
chr2:74281431
|
T | C | 9 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(6): Show | 9 | HG01243.hp2 HG02280.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.401+4342A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74281431 | ||||||
chr2:74281517
|
T | A | 1 | a0001c0001t0002g0053 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.401+4256A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74281517 | ||||||
chr2:74281729
|
C | T | 33 | a0001c0001t0001g0034a0001c0001t0001g0068a0001c0001t0001g0080others(30): Show | 33 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.401+4044G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74281729 | ||||||
chr2:74281950
|
C | G | 5 | a0001c0001t0001g0093a0001c0001t0007g0016a0001c0001t0011g0162others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.401+3823G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74281950 | ||||||
chr2:74282277
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.401+3496C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74282277 | ||||||
chr2:74282533
|
T | C | 5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.401+3240A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74282533 | ||||||
chr2:74282729
|
G | T | 4 | a0001c0001t0001g0084a0001c0001t0001g0109a0001c0001t0026g0107others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.401+3044C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74282729 | ||||||
chr2:74282735
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.401+3038G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74282735 | ||||||
chr2:74282818
|
G | A | 1 | a0001c0003t0003g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.401+2955C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74282818 | ||||||
chr2:74282857
|
G | T | 3 | a0001c0001t0008g0017a0001c0002t0001g0021a0001c0002t0001g0092 | 3 | HG02630.hp2 HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.401+2916C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74282857 | ||||||
chr2:74283014
|
A | G | 4 | a0001c0001t0002g0069a0001c0001t0003g0203a0001c0003t0003g0081others(1): Show | 4 | HG01123.hp2 HG01975.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.401+2759T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74283014 | ||||||
chr2:74283018
|
T | G | 1 | a0002c0004t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.401+2755A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74283018 | ||||||
chr2:74283267
|
C | G | 1 | a0001c0001t0011g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.401+2506G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74283267 | ||||||
chr2:74283389
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0232 | 2 | HG02040.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.401+2384G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74283389 | ||||||
chr2:74283767
|
G | A | 88 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(85): Show | 88 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.401+2006C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74283767 | ||||||
chr2:74283838
|
C | CT | 11 | a0001c0002t0001g0154a0002c0004t0001g0173a0002c0004t0003g0168others(8): Show | 11 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.401+1934dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74283838 | ||||||
chr2:74283838
|
CT | C | 14 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0002g0199others(11): Show | 14 | HG00735.hp2 HG01256.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.401+1934delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74283838 | ||||||
chr2:74283979
|
A | T | 2 | a0001c0001t0001g0196a0001c0001t0022g0197 | 2 | HG01070.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.401+1794T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74283979 | ||||||
chr2:74284149
|
TTATTCCT others(323): Show |
T | 172 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(169): Show | 172 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.401+1294_401+1623d others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74284149 | ||||||
chr2:74284460
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.401+1313C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74284460 | ||||||
chr2:74284471
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.401+1302G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74284471 | ||||||
chr2:74284475
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.401+1298G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74284475 | ||||||
chr2:74284476
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.401+1297C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74284476 | ||||||
chr2:74284616
|
C | T | 153 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(150): Show | 153 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.401+1157G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74284616 | ||||||
chr2:74284796
|
C | T | 83 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(80): Show | 83 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.401+977G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74284796 | ||||||
chr2:74284835
|
G | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0266 | 2 | HG01167.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.401+938C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74284835 | ||||||
chr2:74285016
|
C | A | 9 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(6): Show | 9 | HG01243.hp2 HG02280.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.401+757G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74285016 | ||||||
chr2:74285160
|
A | G | 5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.401+613T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74285160 | ||||||
chr2:74285267
|
G | A | 11 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(8): Show | 11 | HG01243.hp2 HG02280.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.401+506C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74285267 | ||||||
chr2:74285470
|
G | A | 151 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(148): Show | 151 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.401+303C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74285470 | ||||||
chr2:74285642
|
G | C | 4 | a0001c0002t0001g0005a0001c0003t0003g0007a0001c0007t0004g0006others(1): Show | 4 | HG01243.hp2 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.401+131C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74285642 | ||||||
chr2:74285673
|
G | A | 64 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.401+100C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74285673 | ||||||
chr2:74285681
|
G | A | 53 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0068others(50): Show | 53 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.401+92C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74285681 | ||||||
chr2:74285755
|
C | T | 1 | a0001c0002t0001g0119 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.401+18G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74285755 | ||||||
chr2:74285765
|
C | T | 14 | a0002c0004t0001g0104a0002c0004t0001g0173a0002c0004t0003g0168others(11): Show | 14 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.401+8G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 8/30 | chr2 | 74285765 | ||||||
chr2:74286061
|
A | G | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.272-159T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74286061 | ||||||
chr2:74286328
|
A | G | 5 | a0001c0001t0001g0093a0001c0001t0007g0016a0001c0001t0011g0162others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-426T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74286328 | ||||||
chr2:74286539
|
A | C | 60 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0033others(57): Show | 60 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.272-637T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74286539 | ||||||
chr2:74286584
|
C | T | 6 | a0001c0001t0002g0115a0001c0001t0004g0264a0001c0001t0008g0100others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.272-682G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74286584 | ||||||
chr2:74286689
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.272-787A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74286689 | ||||||
chr2:74286782
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.272-880C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74286782 | ||||||
chr2:74286870
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.272-968C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74286870 | ||||||
chr2:74286893
|
C | T | 14 | a0001c0001t0003g0260a0002c0004t0001g0173a0002c0004t0003g0168others(11): Show | 14 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.272-991G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74286893 | ||||||
chr2:74286921
|
A | G | 3 | a0001c0001t0001g0080a0001c0001t0008g0258a0001c0001t0008g0263 | 3 | HG01109.hp1 HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.272-1019T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74286921 | ||||||
chr2:74287037
|
T | C | 5 | a0001c0001t0001g0093a0001c0001t0004g0264a0001c0001t0007g0016others(2): Show | 5 | HG02615.hp2 HG03041.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.272-1135A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74287037 | ||||||
chr2:74287074
|
C | T | 5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-1172G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74287074 | ||||||
chr2:74287540
|
T | C | 180 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0030others(177): Show | 180 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.272-1638A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74287540 | ||||||
chr2:74287668
|
C | T | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.272-1766G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74287668 | ||||||
chr2:74288031
|
G | A | 84 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0030others(81): Show | 84 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.272-2129C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74288031 | ||||||
chr2:74288092
|
C | T | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.272-2190G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74288092 | ||||||
chr2:74288266
|
A | G | 14 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(11): Show | 14 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.272-2364T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74288266 | ||||||
chr2:74288497
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0022g0197 | 2 | HG01070.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.272-2595T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74288497 | ||||||
chr2:74288770
|
T | C | 197 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0030others(194): Show | 197 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.272-2868A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74288770 | ||||||
chr2:74289020
|
G | T | 14 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(11): Show | 14 | HG02280.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.272-3118C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289020 | ||||||
chr2:74289166
|
C | T | 1 | a0002c0004t0001g0219 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.272-3264G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289166 | ||||||
chr2:74289235
|
T | A | 1 | a0007c0015t0001g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.272-3333A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289235 | ||||||
chr2:74289263
|
C | G | 14 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(11): Show | 14 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.272-3361G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289263 | ||||||
chr2:74289323
|
C | CT | 33 | a0001c0001t0001g0034a0001c0001t0001g0095a0001c0001t0001g0097others(30): Show | 33 | HG00735.hp1 HG01192.hp1 HG02280.hp1 others(30): Show |
intron_variant | MODIFIER | c.272-3422dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289323 | ||||||
chr2:74289330
|
T | G | 1 | a0001c0001t0001g0266 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.272-3428A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289330 | ||||||
chr2:74289371
|
C | T | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.272-3469G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289371 | ||||||
chr2:74289498
|
G | A | 1 | a0001c0003t0003g0234 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.272-3596C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289498 | ||||||
chr2:74289543
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.272-3641G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289543 | ||||||
chr2:74289611
|
C | T | 5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-3709G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289611 | ||||||
chr2:74289719
|
T | C | 1 | a0001c0001t0011g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.272-3817A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289719 | ||||||
chr2:74289801
|
G | C | 110 | a0001c0001t0001g0033a0001c0001t0001g0086a0001c0001t0001g0095others(107): Show | 110 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.272-3899C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74289801 | ||||||
chr2:74290026
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(1): Show | 4 | HG01192.hp1 HG02896.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-4124C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290026 | ||||||
chr2:74290037
|
ACCCAGCC others(8): Show |
A | 5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-4150_272-4136d others(17): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290037 | ||||||
chr2:74290124
|
C | A | 105 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0097others(102): Show | 105 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.272-4222G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290124 | ||||||
chr2:74290285
|
G | A | 1 | a0005c0012t0002g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.272-4383C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290285 | ||||||
chr2:74290339
|
C | A | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.272-4437G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290339 | ||||||
chr2:74290472
|
G | C | 8 | a0001c0001t0001g0114a0001c0001t0004g0157a0001c0001t0007g0163others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.272-4570C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290472 | ||||||
chr2:74290553
|
A | G | 64 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(61): Show | 64 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.272-4651T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290553 | ||||||
chr2:74290607
|
AGAGAGAC others(11): Show |
A | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.272-4723_272-4706d others(20): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290607 | ||||||
chr2:74290622
|
T | TGA | 10 | a0001c0001t0002g0075a0001c0001t0004g0264a0001c0001t0008g0017others(7): Show | 10 | HG00609.hp2 HG00673.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.272-4722_272-4721d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGA | 14 | a0001c0001t0002g0022a0001c0001t0002g0115a0001c0001t0008g0100others(11): Show | 14 | HG01257.hp1 HG01257.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.272-4724_272-4721d others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGAGA | 17 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0190others(14): Show | 17 | HG01243.hp2 HG02280.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.272-4726_272-4721d others(8): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGAGAG others(1): Show |
5 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(2): Show | 5 | HG01192.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.272-4728_272-4721d others(10): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGAGAG others(3): Show |
3 | a0001c0001t0002g0131a0001c0001t0007g0159a0001c0002t0002g0126 | 3 | HG02132.hp1 HG02145.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.272-4730_272-4721d others(12): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGAGAG others(5): Show |
10 | a0001c0001t0001g0160a0001c0001t0002g0121a0001c0001t0008g0183others(7): Show | 10 | HG01070.hp2 HG01081.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.272-4732_272-4721d others(14): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGAGAG others(7): Show |
13 | a0001c0001t0002g0174a0001c0001t0002g0176a0001c0001t0002g0204others(10): Show | 13 | HG00735.hp1 HG02155.hp1 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.272-4734_272-4721d others(16): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGAGAG others(9): Show |
22 | a0001c0001t0001g0165a0001c0001t0001g0223a0001c0001t0002g0116others(19): Show | 22 | HG00558.hp2 HG01109.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.272-4736_272-4721d others(18): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGAGAG others(11): Show |
6 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0002g0139others(3): Show | 6 | HG00408.hp2 HG02040.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.272-4738_272-4721d others(20): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGAGAG others(13): Show |
7 | a0001c0001t0002g0128a0001c0001t0002g0145a0001c0001t0002g0146others(4): Show | 7 | HG03453.hp1 NA18956.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.272-4740_272-4721d others(22): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGAGAG others(15): Show |
2 | a0001c0001t0002g0201a0001c0002t0001g0140 | 2 | HG00597.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.272-4742_272-4721d others(24): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
T | TGAGAGAG others(19): Show |
1 | a0001c0003t0003g0224 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.272-4746_272-4721d others(28): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
TGA | T | 3 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0001t0027g0010 | 3 | HG03041.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.272-4722_272-4721d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290622
|
TGAGA | T | 4 | a0001c0001t0001g0213a0001c0001t0002g0214a0001c0003t0003g0208others(1): Show | 4 | HG00280.hp2 HG01346.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-4724_272-4721d others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290622 | ||||||
chr2:74290628
|
A | T | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.272-4726T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290628 | ||||||
chr2:74290731
|
A | T | 1 | a0003c0006t0001g0076 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.272-4829T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290731 | ||||||
chr2:74290827
|
C | T | 1 | a0001c0001t0022g0197 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.272-4925G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74290827 | ||||||
chr2:74291497
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.272-5595C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74291497 | ||||||
chr2:74291498
|
C | T | 1 | a0002c0004t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.272-5596G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74291498 | ||||||
chr2:74291529
|
C | T | 1 | a0002c0004t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.272-5627G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74291529 | ||||||
chr2:74291620
|
A | T | 1 | a0001c0001t0001g0269 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.272-5718T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74291620 | ||||||
chr2:74291657
|
C | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0109a0001c0001t0026g0107others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-5755G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74291657 | ||||||
chr2:74291693
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.272-5791G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74291693 | ||||||
chr2:74291748
|
G | A | 3 | a0001c0003t0003g0191a0001c0003t0003g0245a0001c0003t0003g0246 | 3 | HG02922.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.272-5846C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74291748 | ||||||
chr2:74291871
|
T | C | 5 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0002t0001g0021others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-5969A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74291871 | ||||||
chr2:74291904
|
C | T | 1 | a0002c0004t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.272-6002G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74291904 | ||||||
chr2:74291991
|
G | GT | 14 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(11): Show | 14 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.272-6090dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74291991 | ||||||
chr2:74292081
|
A | G | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.272-6179T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74292081 | ||||||
chr2:74292100
|
C | T | 1 | a0001c0001t0009g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.272-6198G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74292100 | ||||||
chr2:74292113
|
G | T | 6 | a0001c0001t0001g0114a0001c0001t0004g0157a0001c0001t0008g0110others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.272-6211C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74292113 | ||||||
chr2:74292271
|
G | C | 1 | a0001c0001t0004g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.272-6369C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74292271 | ||||||
chr2:74292478
|
G | A | 1 | a0003c0006t0001g0079 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.272-6576C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74292478 | ||||||
chr2:74292854
|
C | T | 62 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(59): Show | 62 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.272-6952G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74292854 | ||||||
chr2:74293306
|
G | A | 6 | a0001c0001t0008g0017a0001c0001t0020g0029a0001c0001t0021g0261others(3): Show | 6 | HG02630.hp2 HG02895.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.272-7404C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74293306 | ||||||
chr2:74293427
|
T | G | 4 | a0001c0002t0001g0005a0001c0003t0003g0007a0001c0007t0004g0006others(1): Show | 4 | HG01243.hp2 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-7525A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74293427 | ||||||
chr2:74293456
|
A | T | 1 | a0001c0001t0001g0097 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.272-7554T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74293456 | ||||||
chr2:74293593
|
G | A | 6 | a0001c0001t0001g0114a0001c0001t0004g0157a0001c0001t0008g0110others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.272-7691C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74293593 | ||||||
chr2:74293620
|
C | A | 1 | a0003c0005t0006g0281 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.272-7718G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74293620 | ||||||
chr2:74293720
|
CA | C | 3 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0001t0027g0010 | 3 | HG03041.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.272-7819delT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74293720 | ||||||
chr2:74294218
|
T | C | 109 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0097others(106): Show | 109 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.272-8316A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74294218 | ||||||
chr2:74294224
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.272-8322G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74294224 | ||||||
chr2:74294284
|
C | T | 96 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0097others(93): Show | 96 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.272-8382G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74294284 | ||||||
chr2:74294494
|
T | C | 1 | a0001c0001t0021g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.272-8592A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74294494 | ||||||
chr2:74294624
|
G | A | 4 | a0001c0002t0001g0005a0001c0003t0003g0007a0001c0007t0004g0006others(1): Show | 4 | HG01243.hp2 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-8722C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74294624 | ||||||
chr2:74294680
|
A | ATT | 12 | a0001c0001t0001g0114a0001c0001t0004g0157a0001c0001t0007g0163others(9): Show | 12 | HG00741.hp1 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.272-8780_272-8779d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74294680 | ||||||
chr2:74294680
|
AT | A | 91 | a0001c0001t0001g0086a0001c0001t0001g0138a0001c0001t0001g0160others(88): Show | 91 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.272-8779delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74294680 | ||||||
chr2:74294757
|
C | T | 6 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0001t0027g0010others(3): Show | 6 | HG03041.hp1 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.272-8855G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74294757 | ||||||
chr2:74294914
|
G | A | 1 | a0001c0003t0003g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.272-9012C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74294914 | ||||||
chr2:74295051
|
T | G | 1 | a0001c0001t0002g0222 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.272-9149A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74295051 | ||||||
chr2:74295151
|
G | A | 1 | a0001c0001t0008g0263 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.272-9249C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74295151 | ||||||
chr2:74295390
|
T | C | 1 | a0003c0005t0001g0227 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.271+9099A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74295390 | ||||||
chr2:74295731
|
C | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0002t0001g0066others(1): Show | 5 | HG02132.hp2 NA18943.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.271+8758G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74295731 | ||||||
chr2:74295862
|
T | G | 1 | a0001c0001t0001g0235 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.271+8627A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74295862 | ||||||
chr2:74296529
|
G | A | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.271+7960C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296529 | ||||||
chr2:74296616
|
C | CA | 33 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0001g0097others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.271+7872dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296616 | ||||||
chr2:74296616
|
C | CAA | 13 | a0001c0001t0002g0115a0001c0001t0004g0264a0001c0001t0008g0100others(10): Show | 13 | HG02451.hp2 HG02647.hp1 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.271+7871_271+7872d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296616 | ||||||
chr2:74296616
|
CA | C | 6 | a0001c0001t0001g0249a0001c0001t0002g0176a0001c0001t0004g0157others(3): Show | 6 | HG01123.hp1 HG02155.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.271+7872delT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296616 | ||||||
chr2:74296655
|
G | T | 20 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(17): Show | 20 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.271+7834C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296655 | ||||||
chr2:74296682
|
A | G | 38 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(35): Show | 38 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.271+7807T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296682 | ||||||
chr2:74296727
|
T | C | 2 | a0001c0001t0002g0069a0003c0005t0001g0085 | 2 | HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.271+7762A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296727 | ||||||
chr2:74296755
|
C | G | 1 | a0001c0002t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.271+7734G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296755 | ||||||
chr2:74296786
|
C | CA | 162 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(159): Show | 163 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.271+7702dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296786 | ||||||
chr2:74296786
|
C | CAA | 8 | a0001c0001t0001g0109a0001c0001t0002g0052a0001c0001t0002g0067others(5): Show | 8 | HG01123.hp2 HG01243.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.271+7701_271+7702d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296786 | ||||||
chr2:74296920
|
T | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+7569A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74296920 | ||||||
chr2:74297031
|
T | C | 1 | a0001c0002t0001g0142 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.271+7458A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74297031 | ||||||
chr2:74297183
|
T | TG | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+7305_271+7306i others(3): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74297183 | ||||||
chr2:74297222
|
G | T | 84 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(81): Show | 85 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.271+7267C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74297222 | ||||||
chr2:74297358
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.271+7131A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74297358 | ||||||
chr2:74297389
|
C | T | 1 | a0001c0001t0003g0061 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.271+7100G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74297389 | ||||||
chr2:74297431
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(88): Show | 92 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.271+7058A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74297431 | ||||||
chr2:74297500
|
A | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+6989T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74297500 | ||||||
chr2:74297594
|
A | G | 4 | a0001c0002t0001g0005a0001c0003t0003g0007a0001c0007t0004g0006others(1): Show | 4 | HG01243.hp2 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+6895T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74297594 | ||||||
chr2:74297931
|
A | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+6558T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74297931 | ||||||
chr2:74298212
|
G | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0052 | 2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.271+6277C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74298212 | ||||||
chr2:74298229
|
T | G | 1 | a0001c0002t0001g0143 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.271+6260A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74298229 | ||||||
chr2:74298646
|
T | C | 29 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(26): Show | 29 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.271+5843A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74298646 | ||||||
chr2:74298723
|
T | C | 1 | a0001c0001t0003g0260 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.271+5766A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74298723 | ||||||
chr2:74299010
|
C | T | 30 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0033others(27): Show | 30 | HG00558.hp1 HG00609.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.271+5479G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299010 | ||||||
chr2:74299070
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.271+5419C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299070 | ||||||
chr2:74299132
|
CCT | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+5355_271+5356d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299132 | ||||||
chr2:74299246
|
G | C | 78 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0160others(75): Show | 78 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.271+5243C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299246 | ||||||
chr2:74299255
|
A | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(122): Show | 126 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.271+5234T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299255 | ||||||
chr2:74299318
|
T | TC | 3 | a0001c0001t0001g0109a0001c0001t0026g0107a0001c0002t0001g0108 | 3 | HG02258.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.271+5170dupG | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299318 | ||||||
chr2:74299338
|
C | T | 73 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0160others(70): Show | 73 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.271+5151G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299338 | ||||||
chr2:74299349
|
C | T | 1 | a0001c0001t0002g0050 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.271+5140G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299349 | ||||||
chr2:74299407
|
C | T | 1 | a0001c0003t0003g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.271+5082G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299407 | ||||||
chr2:74299421
|
C | T | 1 | a0001c0001t0016g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271+5068G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299421 | ||||||
chr2:74299686
|
C | T | 1 | a0001c0001t0016g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271+4803G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299686 | ||||||
chr2:74299738
|
G | T | 2 | a0001c0001t0001g0196a0001c0001t0022g0197 | 2 | HG01070.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.271+4751C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299738 | ||||||
chr2:74299787
|
A | G | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.271+4702T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299787 | ||||||
chr2:74299825
|
T | TA | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+4663dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299825 | ||||||
chr2:74299963
|
C | T | 1 | a0004c0009t0007g0106 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.271+4526G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74299963 | ||||||
chr2:74300020
|
A | G | 1 | a0001c0001t0004g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.271+4469T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300020 | ||||||
chr2:74300057
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.271+4432A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300057 | ||||||
chr2:74300075
|
C | T | 1 | a0002c0004t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.271+4414G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300075 | ||||||
chr2:74300160
|
T | C | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.271+4329A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300160 | ||||||
chr2:74300346
|
T | A | 26 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(23): Show | 26 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.271+4143A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300346 | ||||||
chr2:74300648
|
T | C | 2 | a0001c0003t0003g0078a0003c0006t0001g0079 | 2 | HG02040.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.271+3841A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300648 | ||||||
chr2:74300686
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.271+3803G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300686 | ||||||
chr2:74300687
|
G | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+3802C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300687 | ||||||
chr2:74300759
|
A | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+3730T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300759 | ||||||
chr2:74300829
|
C | G | 78 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0160others(75): Show | 78 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.271+3660G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300829 | ||||||
chr2:74300900
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0002g0009 | 2 | HG03831.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.271+3589A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300900 | ||||||
chr2:74300905
|
T | C | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.271+3584A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300905 | ||||||
chr2:74300952
|
C | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+3537G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300952 | ||||||
chr2:74300977
|
A | G | 1 | a0003c0005t0001g0070 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.271+3512T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74300977 | ||||||
chr2:74301025
|
T | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+3464A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74301025 | ||||||
chr2:74301058
|
T | C | 2 | a0001c0001t0001g0223a0001c0003t0003g0224 | 2 | HG02135.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.271+3431A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74301058 | ||||||
chr2:74301162
|
T | C | 14 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(11): Show | 14 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.271+3327A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74301162 | ||||||
chr2:74301560
|
T | C | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.271+2929A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74301560 | ||||||
chr2:74301638
|
C | T | 1 | a0001c0013t0003g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.271+2851G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74301638 | ||||||
chr2:74301652
|
G | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+2837C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74301652 | ||||||
chr2:74301773
|
C | T | 1 | a0001c0001t0008g0263 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.271+2716G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74301773 | ||||||
chr2:74301837
|
C | G | 1 | a0001c0002t0002g0126 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.271+2652G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74301837 | ||||||
chr2:74301869
|
C | T | 1 | a0001c0001t0012g0212 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.271+2620G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74301869 | ||||||
chr2:74301908
|
G | T | 12 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(9): Show | 12 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.271+2581C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74301908 | ||||||
chr2:74302122
|
A | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+2367T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74302122 | ||||||
chr2:74302223
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.271+2266A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74302223 | ||||||
chr2:74302638
|
C | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+1851G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74302638 | ||||||
chr2:74302789
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.271+1700G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74302789 | ||||||
chr2:74303016
|
C | CTG | 34 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(31): Show | 34 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.271+1471_271+1472d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303016 | ||||||
chr2:74303016
|
C | CTGTG | 4 | a0001c0001t0002g0124a0001c0001t0011g0103a0002c0010t0004g0105others(1): Show | 4 | HG01884.hp1 HG02257.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+1469_271+1472d others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303016 | ||||||
chr2:74303016
|
CTG | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(90): Show | 94 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.271+1471_271+1472d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303016 | ||||||
chr2:74303016
|
CTGTG | C | 3 | a0001c0001t0001g0231a0001c0001t0010g0278a0001c0001t0010g0279 | 3 | HG03098.hp2 HG03486.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.271+1469_271+1472d others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303016 | ||||||
chr2:74303053
|
G | A | 6 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0002t0001g0005others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.271+1436C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303053 | ||||||
chr2:74303064
|
T | G | 1 | a0001c0002t0001g0122 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.271+1425A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303064 | ||||||
chr2:74303117
|
CGTGT | C | 3 | a0001c0001t0003g0195a0002c0004t0001g0271a0002c0004t0002g0210 | 3 | HG02735.hp2 NA18939.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.271+1368_271+1371d others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303117 | ||||||
chr2:74303292
|
G | C | 1 | a0001c0001t0001g0226 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.271+1197C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303292 | ||||||
chr2:74303444
|
A | G | 1 | a0001c0003t0005g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.271+1045T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303444 | ||||||
chr2:74303616
|
A | C | 4 | a0001c0002t0001g0005a0001c0003t0003g0007a0001c0007t0004g0006others(1): Show | 4 | HG01243.hp2 HG03209.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+873T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303616 | ||||||
chr2:74303785
|
A | C | 6 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0002t0001g0005others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.271+704T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303785 | ||||||
chr2:74303786
|
T | C | 13 | a0001c0001t0007g0155a0001c0001t0019g0161a0001c0002t0001g0154others(10): Show | 13 | HG01884.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.271+703A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303786 | ||||||
chr2:74303788
|
T | G | 1 | a0001c0001t0023g0055 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.271+701A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303788 | ||||||
chr2:74303851
|
A | T | 3 | a0001c0001t0001g0109a0001c0001t0026g0107a0001c0002t0001g0108 | 3 | HG02258.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.271+638T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303851 | ||||||
chr2:74303851
|
AT | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(186): Show | 190 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.271+637delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303851 | ||||||
chr2:74303854
|
T | A | 12 | a0001c0001t0001g0114a0001c0001t0001g0196a0001c0001t0001g0198others(9): Show | 12 | HG00741.hp1 HG01070.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.271+635A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303854 | ||||||
chr2:74303855
|
T | A | 77 | a0001c0001t0001g0082a0001c0001t0001g0095a0001c0001t0001g0097others(74): Show | 77 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.271+634A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303855 | ||||||
chr2:74303858
|
T | A | 7 | a0001c0001t0002g0120a0001c0001t0008g0100a0001c0001t0011g0103others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+631A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303858 | ||||||
chr2:74303873
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.271+616C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303873 | ||||||
chr2:74303998
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.271+491G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74303998 | ||||||
chr2:74304060
|
G | A | 12 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(9): Show | 12 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.271+429C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74304060 | ||||||
chr2:74304096
|
A | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.271+393T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74304096 | ||||||
chr2:74304129
|
G | A | 1 | a0001c0003t0003g0156 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.271+360C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74304129 | ||||||
chr2:74304174
|
C | T | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.271+315G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74304174 | ||||||
chr2:74304261
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.271+228G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74304261 | ||||||
chr2:74304280
|
G | C | 5 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0003t0003g0007others(2): Show | 5 | HG03098.hp2 HG03209.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.271+209C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74304280 | ||||||
chr2:74304293
|
T | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(202): Show | 206 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.271+196A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74304293 | ||||||
chr2:74304456
|
G | A | 76 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0160others(73): Show | 76 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.271+33C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 7/30 | chr2 | 74304456 | ||||||
chr2:74304954
|
G | T | 4 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(1): Show | 4 | HG01192.hp1 HG02896.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-274C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74304954 | ||||||
chr2:74304979
|
A | G | 1 | a0001c0002t0002g0149 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.80-299T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74304979 | ||||||
chr2:74304998
|
C | A | 7 | a0001c0001t0002g0115a0001c0001t0008g0100a0001c0001t0011g0103others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-318G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74304998 | ||||||
chr2:74305422
|
T | C | 1 | a0003c0005t0002g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.80-742A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74305422 | ||||||
chr2:74305433
|
C | T | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.80-753G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74305433 | ||||||
chr2:74305442
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(120): Show | 124 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.80-762A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74305442 | ||||||
chr2:74305462
|
C | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-782G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74305462 | ||||||
chr2:74305616
|
A | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-936T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74305616 | ||||||
chr2:74305645
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.80-965A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74305645 | ||||||
chr2:74305678
|
C | CTCTTCA | 14 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(11): Show | 14 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.80-1004_80-999dupT others(5): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74305678 | ||||||
chr2:74305721
|
C | CT | 25 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0093others(22): Show | 25 | HG00741.hp1 HG01192.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.80-1042dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74305721 | ||||||
chr2:74305721
|
CT | C | 79 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0160others(76): Show | 79 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.80-1042delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74305721 | ||||||
chr2:74305946
|
G | A | 1 | a0001c0001t0011g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-1266C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74305946 | ||||||
chr2:74306001
|
G | A | 1 | a0001c0001t0009g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.80-1321C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306001 | ||||||
chr2:74306105
|
T | C | 1 | a0001c0001t0008g0263 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.80-1425A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306105 | ||||||
chr2:74306121
|
C | T | 4 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0002t0001g0186others(1): Show | 4 | HG02280.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-1441G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306121 | ||||||
chr2:74306356
|
A | AT | 26 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(23): Show | 26 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.80-1677_80-1676ins others(1): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306356 | ||||||
chr2:74306371
|
A | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-1691T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306371 | ||||||
chr2:74306492
|
G | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-1812C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306492 | ||||||
chr2:74306512
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(119): Show | 123 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.80-1832G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306512 | ||||||
chr2:74306652
|
CT | C | 115 | a0001c0001t0001g0026a0001c0001t0001g0095a0001c0001t0001g0097others(112): Show | 115 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.80-1973delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306652 | ||||||
chr2:74306684
|
T | C | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | NA19004.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.80-2004A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306684 | ||||||
chr2:74306695
|
C | T | 11 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(8): Show | 11 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-2015G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306695 | ||||||
chr2:74306997
|
T | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-2317A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74306997 | ||||||
chr2:74307050
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.80-2370G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307050 | ||||||
chr2:74307056
|
C | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-2376G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307056 | ||||||
chr2:74307126
|
T | C | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.80-2446A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307126 | ||||||
chr2:74307228
|
G | A | 1 | a0001c0001t0016g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.80-2548C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307228 | ||||||
chr2:74307240
|
G | C | 27 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(24): Show | 27 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.80-2560C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307240 | ||||||
chr2:74307244
|
C | A | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.80-2564G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307244 | ||||||
chr2:74307245
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.80-2565A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307245 | ||||||
chr2:74307247
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(120): Show | 124 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.80-2567T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307247 | ||||||
chr2:74307253
|
T | C | 13 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(10): Show | 13 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-2573A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307253 | ||||||
chr2:74307281
|
T | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-2601A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307281 | ||||||
chr2:74307296
|
T | G | 1 | a0001c0001t0003g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.80-2616A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307296 | ||||||
chr2:74307367
|
G | A | 2 | a0001c0001t0002g0069a0003c0005t0001g0085 | 2 | HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.80-2687C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307367 | ||||||
chr2:74307468
|
G | A | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.80-2788C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307468 | ||||||
chr2:74307476
|
C | T | 1 | a0001c0003t0003g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.80-2796G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307476 | ||||||
chr2:74307564
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(121): Show | 125 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.80-2884A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307564 | ||||||
chr2:74307588
|
C | T | 1 | a0002c0004t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.80-2908G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307588 | ||||||
chr2:74307664
|
C | T | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.80-2984G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307664 | ||||||
chr2:74307674
|
C | A | 2 | a0002c0004t0001g0271a0002c0004t0002g0210 | 2 | HG02735.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.80-2994G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307674 | ||||||
chr2:74307676
|
G | C | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.80-2996C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307676 | ||||||
chr2:74307817
|
T | TG | 280 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(277): Show | 281 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.80-3138dupC | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307817 | ||||||
chr2:74307891
|
C | T | 13 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(10): Show | 13 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-3211G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307891 | ||||||
chr2:74307936
|
C | T | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.80-3256G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307936 | ||||||
chr2:74307937
|
G | A | 2 | a0001c0001t0002g0069a0003c0005t0001g0085 | 2 | HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.80-3257C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307937 | ||||||
chr2:74307982
|
G | A | 13 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(10): Show | 13 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.80-3302C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74307982 | ||||||
chr2:74308223
|
A | G | 1 | a0001c0001t0006g0211 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.80-3543T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308223 | ||||||
chr2:74308267
|
G | C | 14 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(11): Show | 14 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-3587C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308267 | ||||||
chr2:74308327
|
G | A | 1 | a0005c0012t0002g0041 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.80-3647C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308327 | ||||||
chr2:74308405
|
T | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-3725A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308405 | ||||||
chr2:74308427
|
G | A | 1 | a0001c0003t0003g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.80-3747C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308427 | ||||||
chr2:74308483
|
G | T | 1 | a0002c0004t0001g0104 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.80-3803C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308483 | ||||||
chr2:74308502
|
T | C | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.80-3822A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308502 | ||||||
chr2:74308613
|
G | T | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.80-3933C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308613 | ||||||
chr2:74308728
|
C | T | 1 | a0001c0003t0005g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.80-4048G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308728 | ||||||
chr2:74308738
|
A | AT | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.80-4059dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308738 | ||||||
chr2:74308738
|
AT | A | 10 | a0001c0001t0004g0264a0001c0001t0008g0100a0001c0001t0010g0278others(7): Show | 10 | HG02451.hp2 HG02970.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-4059delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308738 | ||||||
chr2:74308738
|
ATT | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-4060_80-4059del others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308738 | ||||||
chr2:74308918
|
A | ATT | 11 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(8): Show | 11 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.80-4240_80-4239dup others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74308918 | ||||||
chr2:74309080
|
A | AT | 28 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.80-4401dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74309080 | ||||||
chr2:74309226
|
AT | A | 14 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(11): Show | 14 | HG00735.hp1 HG00741.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.80-4547delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74309226 | ||||||
chr2:74309646
|
T | G | 1 | a0001c0001t0011g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.80-4966A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74309646 | ||||||
chr2:74309656
|
A | AT | 8 | a0001c0001t0001g0082a0001c0001t0002g0115a0001c0001t0002g0116others(5): Show | 8 | HG02083.hp2 HG02451.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-4977dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74309656 | ||||||
chr2:74309656
|
A | T | 2 | a0001c0001t0002g0069a0003c0005t0001g0085 | 2 | HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.80-4976T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74309656 | ||||||
chr2:74309853
|
G | A | 4 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(1): Show | 4 | NA18975.hp1 NA19007.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+5092C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74309853 | ||||||
chr2:74309952
|
G | A | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.79+4993C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74309952 | ||||||
chr2:74309962
|
A | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+4983T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74309962 | ||||||
chr2:74310139
|
T | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+4806A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74310139 | ||||||
chr2:74310517
|
T | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+4428A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74310517 | ||||||
chr2:74310573
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(202): Show | 206 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.79+4372G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74310573 | ||||||
chr2:74310606
|
T | A | 1 | a0001c0001t0027g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.79+4339A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74310606 | ||||||
chr2:74310688
|
T | C | 13 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(10): Show | 13 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.79+4257A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74310688 | ||||||
chr2:74310784
|
C | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+4161G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74310784 | ||||||
chr2:74310961
|
A | AATT | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+3981_79+3983dup others(3): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74310961 | ||||||
chr2:74311094
|
C | T | 30 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(27): Show | 30 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.79+3851G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74311094 | ||||||
chr2:74311188
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.79+3757G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74311188 | ||||||
chr2:74311357
|
A | G | 1 | a0001c0001t0016g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79+3588T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74311357 | ||||||
chr2:74311408
|
T | C | 11 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(8): Show | 11 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+3537A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74311408 | ||||||
chr2:74311732
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0005g0272 | 2 | NA18973.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.79+3213A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74311732 | ||||||
chr2:74311868
|
CT | C | 12 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(9): Show | 12 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.79+3076delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74311868 | ||||||
chr2:74312048
|
T | G | 3 | a0001c0001t0001g0230a0001c0001t0003g0205a0001c0002t0001g0185 | 3 | HG00741.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.79+2897A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312048 | ||||||
chr2:74312239
|
GTA | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0082a0001c0001t0002g0009others(1): Show | 4 | HG01256.hp2 HG02165.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+2704_79+2705del others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312239 | ||||||
chr2:74312241
|
A | ATG | 15 | a0001c0001t0001g0054a0001c0001t0001g0084a0001c0001t0001g0090others(12): Show | 15 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+2703_79+2704ins others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312241 | ||||||
chr2:74312243
|
A | ATG | 10 | a0001c0001t0009g0187a0001c0001t0009g0189a0001c0001t0011g0103others(7): Show | 10 | HG00735.hp1 HG01884.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+2700_79+2701dup others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312243 | ||||||
chr2:74312243
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(85): Show | 89 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.79+2702T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312243 | ||||||
chr2:74312243
|
ATGTGTGT others(3): Show |
A | 6 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0002t0001g0005others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+2692_79+2701del others(10): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312243 | ||||||
chr2:74312273
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.79+2672T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312273 | ||||||
chr2:74312292
|
C | T | 1 | a0001c0001t0011g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.79+2653G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312292 | ||||||
chr2:74312332
|
C | G | 30 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(27): Show | 30 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.79+2613G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312332 | ||||||
chr2:74312418
|
C | T | 1 | a0001c0001t0003g0203 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.79+2527G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312418 | ||||||
chr2:74312758
|
T | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(121): Show | 125 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.79+2187A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312758 | ||||||
chr2:74312967
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(120): Show | 124 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.79+1978T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312967 | ||||||
chr2:74312982
|
T | G | 3 | a0001c0001t0002g0121a0001c0002t0001g0122a0001c0002t0001g0123 | 3 | HG01081.hp2 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.79+1963A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74312982 | ||||||
chr2:74313016
|
C | CT | 6 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0002t0001g0005others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+1928dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74313016 | ||||||
chr2:74313016
|
CT | C | 13 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0006g0236others(10): Show | 13 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.79+1928delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74313016 | ||||||
chr2:74313049
|
CT | C | 19 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0001g0231others(16): Show | 19 | HG00735.hp1 HG00741.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.79+1895delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74313049 | ||||||
chr2:74313251
|
A | C | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.79+1694T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74313251 | ||||||
chr2:74313481
|
G | C | 3 | a0001c0001t0007g0163a0001c0001t0011g0162a0007c0015t0001g0164 | 3 | HG01891.hp1 HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.79+1464C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74313481 | ||||||
chr2:74313790
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.79+1155G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74313790 | ||||||
chr2:74313850
|
T | G | 6 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0002t0001g0005others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+1095A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74313850 | ||||||
chr2:74313868
|
T | C | 8 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0008g0110others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.79+1077A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74313868 | ||||||
chr2:74313913
|
G | A | 1 | a0001c0003t0005g0182 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.79+1032C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74313913 | ||||||
chr2:74314060
|
T | C | 1 | a0001c0003t0003g0274 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.79+885A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74314060 | ||||||
chr2:74314411
|
G | C | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.79+534C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74314411 | ||||||
chr2:74314921
|
A | C | 1 | a0001c0003t0003g0208 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.79+24T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 6/30 | chr2 | 74314921 | ||||||
chr2:74315398
|
C | T | 6 | a0001c0001t0002g0275a0001c0003t0003g0191a0001c0003t0003g0245others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-373G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74315398 | ||||||
chr2:74315441
|
C | T | 3 | a0001c0003t0003g0078a0003c0005t0001g0077a0003c0006t0001g0079 | 3 | HG02040.hp2 NA18939.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-2-416G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74315441 | ||||||
chr2:74315447
|
GA | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(169): Show | 173 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.-2-423delT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74315447 | ||||||
chr2:74315447
|
GAA | G | 29 | a0001c0001t0001g0026a0001c0001t0001g0095a0001c0001t0001g0097others(26): Show | 29 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.-2-424_-2-423delTT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74315447 | ||||||
chr2:74315564
|
C | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(200): Show | 204 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.-2-539G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74315564 | ||||||
chr2:74315614
|
A | G | 1 | a0001c0002t0001g0207 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-2-589T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74315614 | ||||||
chr2:74316174
|
C | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-1149G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316174 | ||||||
chr2:74316321
|
T | TA | 13 | a0001c0001t0001g0235a0001c0001t0002g0237a0001c0001t0002g0239others(10): Show | 13 | HG01175.hp2 HG01928.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2-1297dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316321 | ||||||
chr2:74316321
|
TA | T | 87 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0114others(84): Show | 87 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.-2-1297delT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316321 | ||||||
chr2:74316321
|
TAA | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-2-1298_-2-1297del others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316321 | ||||||
chr2:74316321
|
TAAA | T | 12 | a0001c0001t0001g0025a0001c0001t0001g0086a0001c0001t0002g0059others(9): Show | 12 | HG01167.hp2 HG01256.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-1299_-2-1297del others(3): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316321 | ||||||
chr2:74316321
|
TAAAAAAA others(2): Show |
T | 6 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0002t0001g0005others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-1305_-2-1297del others(9): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316321 | ||||||
chr2:74316323
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-2-1298T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316323 | ||||||
chr2:74316324
|
A | T | 6 | a0001c0001t0001g0109a0001c0001t0008g0110a0001c0002t0001g0108others(3): Show | 6 | HG00741.hp1 HG01891.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-1299T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316324 | ||||||
chr2:74316325
|
A | T | 4 | a0001c0001t0007g0163a0001c0001t0011g0162a0001c0001t0026g0107others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-1300T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316325 | ||||||
chr2:74316326
|
A | T | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-2-1301T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316326 | ||||||
chr2:74316403
|
C | T | 1 | a0002c0004t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-2-1378G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316403 | ||||||
chr2:74316465
|
G | A | 64 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0160others(61): Show | 64 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.-2-1440C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316465 | ||||||
chr2:74316468
|
G | A | 12 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(9): Show | 12 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-1443C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316468 | ||||||
chr2:74316551
|
T | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-1526A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316551 | ||||||
chr2:74316724
|
G | A | 2 | a0001c0001t0001g0084a0001c0002t0001g0083 | 2 | HG01261.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-2-1699C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316724 | ||||||
chr2:74316752
|
T | C | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-2-1727A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316752 | ||||||
chr2:74316804
|
C | T | 12 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(9): Show | 12 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-1779G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316804 | ||||||
chr2:74316826
|
C | G | 1 | a0001c0001t0002g0024 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-2-1801G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316826 | ||||||
chr2:74316905
|
C | T | 1 | a0002c0010t0004g0105 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-2-1880G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316905 | ||||||
chr2:74316998
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(200): Show | 204 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.-2-1973G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74316998 | ||||||
chr2:74317180
|
T | C | 2 | a0001c0001t0001g0192a0001c0001t0003g0193 | 2 | HG02258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-2-2155A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74317180 | ||||||
chr2:74317235
|
C | G | 12 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(9): Show | 12 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-2210G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74317235 | ||||||
chr2:74317352
|
GT | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-2-2328delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74317352 | ||||||
chr2:74317352
|
GTT | G | 30 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(27): Show | 30 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2-2329_-2-2328del others(2): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74317352 | ||||||
chr2:74317559
|
T | C | 5 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(2): Show | 5 | HG01192.hp1 HG01243.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-2534A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74317559 | ||||||
chr2:74317906
|
A | G | 1 | a0001c0001t0002g0201 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-2-2881T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74317906 | ||||||
chr2:74318138
|
A | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-3113T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74318138 | ||||||
chr2:74318141
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-2-3116T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74318141 | ||||||
chr2:74318281
|
C | T | 30 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(27): Show | 30 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2-3256G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74318281 | ||||||
chr2:74318370
|
C | T | 1 | a0001c0001t0010g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-2-3345G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74318370 | ||||||
chr2:74318439
|
C | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-2-3414G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74318439 | ||||||
chr2:74318570
|
C | T | 80 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0160others(77): Show | 80 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-2-3545G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74318570 | ||||||
chr2:74318684
|
C | CA | 8 | a0001c0001t0001g0054a0001c0001t0002g0014a0001c0001t0002g0015others(5): Show | 8 | HG00408.hp1 HG00609.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-3660dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74318684 | ||||||
chr2:74318750
|
C | T | 1 | a0001c0001t0016g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2-3725G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74318750 | ||||||
chr2:74318800
|
T | G | 1 | a0001c0001t0007g0159 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-2-3775A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74318800 | ||||||
chr2:74318874
|
T | C | 1 | a0001c0001t0016g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2-3849A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74318874 | ||||||
chr2:74319163
|
G | A | 5 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0243others(2): Show | 5 | HG01175.hp2 HG01928.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-4138C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74319163 | ||||||
chr2:74319296
|
C | G | 1 | a0002c0008t0002g0167 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-2-4271G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74319296 | ||||||
chr2:74319318
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-2-4293A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74319318 | ||||||
chr2:74319375
|
G | A | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-2-4350C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74319375 | ||||||
chr2:74319556
|
A | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-4531T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74319556 | ||||||
chr2:74319589
|
A | T | 1 | a0001c0001t0002g0124 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-2-4564T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74319589 | ||||||
chr2:74319633
|
T | C | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-2-4608A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74319633 | ||||||
chr2:74319766
|
A | C | 4 | a0001c0002t0002g0073a0001c0003t0003g0071a0003c0005t0001g0070others(1): Show | 4 | HG00673.hp1 HG01952.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4741T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74319766 | ||||||
chr2:74319808
|
C | A | 6 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0048others(3): Show | 6 | HG00735.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-4783G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74319808 | ||||||
chr2:74320011
|
C | T | 6 | a0001c0001t0002g0075a0001c0003t0001g0074a0001c0003t0003g0078others(3): Show | 6 | HG00544.hp1 HG00673.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-4986G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320011 | ||||||
chr2:74320021
|
C | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-4996G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320021 | ||||||
chr2:74320034
|
A | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-5009T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320034 | ||||||
chr2:74320155
|
A | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-5130T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320155 | ||||||
chr2:74320167
|
G | C | 1 | a0001c0003t0003g0242 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-2-5142C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320167 | ||||||
chr2:74320221
|
A | T | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-2-5196T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320221 | ||||||
chr2:74320232
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(119): Show | 123 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.-2-5207G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320232 | ||||||
chr2:74320323
|
A | C | 1 | a0001c0001t0001g0023 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-2-5298T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320323 | ||||||
chr2:74320431
|
T | C | 26 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(23): Show | 26 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.-2-5406A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320431 | ||||||
chr2:74320582
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-2-5557G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320582 | ||||||
chr2:74320725
|
T | C | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-2-5700A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320725 | ||||||
chr2:74320744
|
G | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-5719C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320744 | ||||||
chr2:74320975
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-2-5950C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74320975 | ||||||
chr2:74321226
|
C | T | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-2-6201G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74321226 | ||||||
chr2:74321260
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-2-6235A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74321260 | ||||||
chr2:74321494
|
A | G | 4 | a0001c0001t0007g0155a0001c0002t0001g0154a0001c0003t0003g0156others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-6469T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74321494 | ||||||
chr2:74321560
|
A | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-6535T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74321560 | ||||||
chr2:74321680
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(124): Show | 128 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-3+6440T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74321680 | ||||||
chr2:74321816
|
A | C | 2 | a0001c0001t0002g0120a0001c0002t0001g0119 | 2 | NA18977.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-3+6304T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74321816 | ||||||
chr2:74321860
|
A | G | 1 | a0001c0001t0008g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-3+6260T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74321860 | ||||||
chr2:74322023
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0007g0016 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-3+6097G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74322023 | ||||||
chr2:74322117
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-3+6003T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74322117 | ||||||
chr2:74322123
|
C | T | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-3+5997G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74322123 | ||||||
chr2:74322188
|
G | GA | 17 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0002g0050others(14): Show | 17 | HG00735.hp1 HG00741.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-3+5931dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74322188 | ||||||
chr2:74322308
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-3+5812A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74322308 | ||||||
chr2:74322579
|
C | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+5541G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74322579 | ||||||
chr2:74323335
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-3+4785G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74323335 | ||||||
chr2:74324153
|
G | T | 15 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(12): Show | 15 | HG01192.hp1 HG01884.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+3967C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74324153 | ||||||
chr2:74324156
|
C | A | 88 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(85): Show | 89 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-3+3964G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74324156 | ||||||
chr2:74324449
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-3+3671G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74324449 | ||||||
chr2:74325117
|
G | A | 8 | a0002c0004t0001g0173a0002c0004t0003g0168a0002c0004t0003g0169others(5): Show | 8 | HG02486.hp1 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3+3003C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74325117 | ||||||
chr2:74325489
|
G | A | 2 | a0001c0003t0003g0245a0001c0003t0003g0246 | 2 | HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-3+2631C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74325489 | ||||||
chr2:74325560
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0002g0053 | 2 | HG00621.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-3+2560A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74325560 | ||||||
chr2:74325748
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-3+2372C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74325748 | ||||||
chr2:74325883
|
G | GGGGAAGG others(4): Show |
1 | a0001c0001t0016g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-3+2226_-3+2236dup others(11): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74325883 | ||||||
chr2:74325931
|
GAGGAAGG others(4): Show |
G | 1 | a0001c0001t0027g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-3+2178_-3+2188del others(11): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74325931 | ||||||
chr2:74325968
|
A | G | 1 | a0001c0001t0003g0184 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-3+2152T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74325968 | ||||||
chr2:74325972
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-3+2148G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74325972 | ||||||
chr2:74325973
|
G | A | 5 | a0001c0001t0001g0097a0001c0001t0002g0056a0001c0001t0002g0057others(2): Show | 5 | NA18522.hp1 NA18949.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+2147C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74325973 | ||||||
chr2:74326249
|
C | A | 2 | a0001c0001t0001g0248a0001c0001t0006g0247 | 2 | NA19002.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.-3+1871G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74326249 | ||||||
chr2:74326380
|
G | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+1740C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74326380 | ||||||
chr2:74326591
|
C | T | 8 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0008g0110others(5): Show | 8 | HG00741.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3+1529G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74326591 | ||||||
chr2:74326592
|
G | A | 1 | a0001c0001t0015g0102 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-3+1528C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74326592 | ||||||
chr2:74326676
|
G | C | 11 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(8): Show | 11 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3+1444C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74326676 | ||||||
chr2:74326914
|
T | A | 124 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(121): Show | 125 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.-3+1206A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74326914 | ||||||
chr2:74327249
|
C | T | 5 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0003t0003g0007others(2): Show | 5 | HG03098.hp2 HG03209.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+871G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74327249 | ||||||
chr2:74327513
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-3+607C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74327513 | ||||||
chr2:74327690
|
G | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+430C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74327690 | ||||||
chr2:74327782
|
C | T | 1 | a0001c0001t0002g0199 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-3+338G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74327782 | ||||||
chr2:74327803
|
A | T | 8 | a0002c0004t0001g0173a0002c0004t0003g0168a0002c0004t0003g0169others(5): Show | 8 | HG02486.hp1 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3+317T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74327803 | ||||||
chr2:74327807
|
CT | C | 5 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0003t0003g0007others(2): Show | 5 | HG03098.hp2 HG03209.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+312delA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74327807 | ||||||
chr2:74327895
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(1): Show | 4 | HG01192.hp1 HG02896.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+225C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74327895 | ||||||
chr2:74327906
|
C | T | 1 | a0003c0006t0001g0076 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-3+214G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 5/30 | chr2 | 74327906 | ||||||
chr2:74328288
|
C | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-69-102G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74328288 | ||||||
chr2:74328294
|
G | A | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-69-108C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74328294 | ||||||
chr2:74328295
|
G | C | 1 | a0001c0001t0001g0250 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-69-109C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74328295 | ||||||
chr2:74328538
|
G | A | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-69-352C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74328538 | ||||||
chr2:74328618
|
C | A | 1 | a0001c0001t0010g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-69-432G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74328618 | ||||||
chr2:74328840
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0026g0107a0001c0002t0001g0108 | 3 | HG02258.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-69-654C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74328840 | ||||||
chr2:74328882
|
A | G | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-69-696T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74328882 | ||||||
chr2:74328972
|
A | AT | 16 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0002g0115others(13): Show | 16 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-69-787dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74328972 | ||||||
chr2:74329103
|
T | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-69-917A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74329103 | ||||||
chr2:74329263
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-69-1077C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74329263 | ||||||
chr2:74329543
|
A | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-69-1357T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74329543 | ||||||
chr2:74329552
|
G | A | 1 | a0001c0001t0002g0251 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-69-1366C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74329552 | ||||||
chr2:74329587
|
TCAAA | T | 66 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0001g0130others(63): Show | 66 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-69-1405_-69-1402d others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74329587 | ||||||
chr2:74329658
|
G | C | 1 | a0001c0002t0001g0150 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-69-1472C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74329658 | ||||||
chr2:74329731
|
A | G | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-69-1545T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74329731 | ||||||
chr2:74329996
|
G | A | 1 | a0001c0002t0001g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-69-1810C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74329996 | ||||||
chr2:74330036
|
T | G | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-69-1850A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330036 | ||||||
chr2:74330060
|
A | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(203): Show | 207 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.-69-1874T>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330060 | ||||||
chr2:74330095
|
T | C | 1 | a0001c0002t0001g0152 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-69-1909A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330095 | ||||||
chr2:74330305
|
G | A | 1 | a0003c0005t0002g0252 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-69-2119C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330305 | ||||||
chr2:74330537
|
G | A | 2 | a0001c0001t0002g0069a0003c0005t0001g0085 | 2 | HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-69-2351C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330537 | ||||||
chr2:74330567
|
T | A | 10 | a0001c0001t0002g0115a0001c0001t0004g0264a0001c0001t0008g0100others(7): Show | 10 | HG01884.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-69-2381A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330567 | ||||||
chr2:74330626
|
CAGATGGA others(13): Show |
C | 6 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0002t0001g0005others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-2460_-69-2441d others(22): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330626 | ||||||
chr2:74330804
|
G | T | 1 | a0001c0001t0027g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-69-2618C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330804 | ||||||
chr2:74330868
|
A | AGGTGAGG others(56): Show |
279 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(276): Show | 280 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.-69-2683_-69-2682i others(65): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330868 | ||||||
chr2:74330868
|
A | AGGTGAGG others(235): Show |
1 | a0001c0001t0003g0195 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-69-2683_-69-2682i others(244): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330868 | ||||||
chr2:74330885
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(93): Show | 97 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-69-2699T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330885 | ||||||
chr2:74330888
|
T | A | 8 | a0001c0001t0004g0264a0001c0001t0008g0100a0001c0001t0011g0103others(5): Show | 8 | HG01884.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-69-2702A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74330888 | ||||||
chr2:74331150
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-70+2877G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74331150 | ||||||
chr2:74331285
|
T | G | 1 | a0001c0002t0001g0005 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-70+2742A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74331285 | ||||||
chr2:74331431
|
G | T | 6 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0002t0001g0005others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70+2596C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74331431 | ||||||
chr2:74331494
|
T | C | 11 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(8): Show | 11 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-70+2533A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74331494 | ||||||
chr2:74331714
|
C | A | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-70+2313G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74331714 | ||||||
chr2:74332120
|
C | T | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-70+1907G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332120 | ||||||
chr2:74332148
|
C | T | 1 | a0001c0001t0004g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-70+1879G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332148 | ||||||
chr2:74332160
|
T | C | 12 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0007g0163others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-70+1867A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332160 | ||||||
chr2:74332287
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(201): Show | 205 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.-70+1740G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332287 | ||||||
chr2:74332321
|
G | A | 1 | a0001c0001t0004g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-70+1706C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332321 | ||||||
chr2:74332331
|
CAT | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-70+1694_-70+1695d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332331 | ||||||
chr2:74332604
|
T | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(1): Show | 4 | HG01192.hp1 HG02896.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+1423A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332604 | ||||||
chr2:74332678
|
C | T | 1 | a0001c0001t0004g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-70+1349G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332678 | ||||||
chr2:74332703
|
T | TTG | 6 | a0001c0001t0002g0067a0001c0001t0010g0278a0001c0001t0010g0279others(3): Show | 6 | HG02257.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70+1322_-70+1323d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332703 | ||||||
chr2:74332703
|
T | TTGTGTGT others(1): Show |
3 | a0001c0001t0001g0109a0001c0001t0026g0107a0001c0002t0001g0108 | 3 | HG02258.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-70+1316_-70+1323d others(10): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332703 | ||||||
chr2:74332703
|
T | TTGTGTGT others(3): Show |
9 | a0001c0001t0001g0114a0001c0001t0007g0163a0001c0001t0008g0110others(6): Show | 9 | HG00735.hp1 HG00741.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70+1314_-70+1323d others(12): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332703 | ||||||
chr2:74332703
|
TTG | T | 49 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0165others(46): Show | 49 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-70+1322_-70+1323d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332703 | ||||||
chr2:74332722
|
T | C | 1 | a0001c0001t0008g0263 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-70+1305A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332722 | ||||||
chr2:74332724
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-70+1303A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332724 | ||||||
chr2:74332753
|
AAGAG | A | 8 | a0001c0001t0002g0115a0001c0001t0008g0100a0001c0001t0011g0103others(5): Show | 8 | HG01884.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-70+1270_-70+1273d others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332753 | ||||||
chr2:74332850
|
C | A | 1 | a0001c0001t0011g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-70+1177G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332850 | ||||||
chr2:74332875
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(89): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-70+1152G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332875 | ||||||
chr2:74332960
|
C | G | 1 | a0001c0002t0001g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-70+1067G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332960 | ||||||
chr2:74332994
|
C | A | 1 | a0001c0001t0011g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-70+1033G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74332994 | ||||||
chr2:74333455
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(88): Show | 92 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-70+572A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74333455 | ||||||
chr2:74333784
|
C | G | 2 | a0001c0001t0002g0075a0001c0003t0001g0074 | 2 | HG00544.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.-70+243G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 4/30 | chr2 | 74333784 | ||||||
chr2:74334343
|
C | T | 1 | a0001c0001t0003g0194 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-220-166G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74334343 | ||||||
chr2:74334384
|
C | T | 4 | a0001c0002t0002g0073a0001c0003t0003g0071a0003c0005t0001g0070others(1): Show | 4 | HG00673.hp1 HG01952.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-220-207G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74334384 | ||||||
chr2:74334590
|
T | G | 14 | a0001c0001t0001g0086a0001c0001t0002g0062a0001c0001t0002g0063others(11): Show | 14 | HG00438.hp1 HG00621.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.-220-413A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74334590 | ||||||
chr2:74334706
|
A | C | 1 | a0001c0001t0002g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-220-529T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74334706 | ||||||
chr2:74334721
|
C | T | 17 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0002g0115others(14): Show | 17 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-220-544G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74334721 | ||||||
chr2:74334733
|
C | CT | 9 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(6): Show | 9 | HG01192.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-220-557dupA | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74334733 | ||||||
chr2:74334763
|
G | GA | 7 | a0001c0001t0001g0068a0001c0001t0010g0278a0001c0001t0010g0279others(4): Show | 7 | HG01243.hp2 HG03098.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-220-587dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74334763 | ||||||
chr2:74334976
|
CTT | C | 17 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0002g0115others(14): Show | 17 | HG00741.hp1 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-220-801_-220-800d others(4): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74334976 | ||||||
chr2:74335013
|
G | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(118): Show | 122 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-220-836C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74335013 | ||||||
chr2:74335086
|
A | G | 1 | a0001c0001t0008g0017 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-220-909T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74335086 | ||||||
chr2:74335181
|
A | G | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-220-1004T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74335181 | ||||||
chr2:74335253
|
A | C | 2 | a0001c0001t0001g0192a0001c0001t0003g0193 | 2 | HG02258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-220-1076T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74335253 | ||||||
chr2:74335271
|
G | A | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-220-1094C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74335271 | ||||||
chr2:74335333
|
A | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(62): Show | 66 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.-220-1156T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74335333 | ||||||
chr2:74335714
|
A | C | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-220-1537T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74335714 | ||||||
chr2:74335797
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0007g0016 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-220-1620G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74335797 | ||||||
chr2:74335840
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0003t0003g0094 | 3 | NA18956.hp2 NA19009.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-220-1663A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74335840 | ||||||
chr2:74335891
|
T | A | 1 | a0001c0001t0027g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-220-1714A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74335891 | ||||||
chr2:74336022
|
T | G | 1 | a0001c0001t0008g0263 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-220-1845A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74336022 | ||||||
chr2:74336032
|
A | G | 19 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0002g0115others(16): Show | 19 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.-220-1855T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74336032 | ||||||
chr2:74336171
|
G | A | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-220-1994C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74336171 | ||||||
chr2:74336360
|
C | T | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-220-2183G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74336360 | ||||||
chr2:74336361
|
G | A | 8 | a0002c0004t0001g0173a0002c0004t0003g0168a0002c0004t0003g0169others(5): Show | 8 | HG02486.hp1 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-220-2184C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74336361 | ||||||
chr2:74336685
|
G | A | 1 | a0001c0001t0016g0003 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-221+2170C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74336685 | ||||||
chr2:74336841
|
C | T | 28 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0109others(25): Show | 28 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.-221+2014G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74336841 | ||||||
chr2:74337133
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-221+1722G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74337133 | ||||||
chr2:74337284
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(87): Show | 91 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-221+1571T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74337284 | ||||||
chr2:74337366
|
C | G | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | HG01070.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-221+1489G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74337366 | ||||||
chr2:74337414
|
CA | C | 5 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0003t0003g0007others(2): Show | 5 | HG03098.hp2 HG03209.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-221+1440delT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74337414 | ||||||
chr2:74337486
|
C | G | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-221+1369G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74337486 | ||||||
chr2:74337930
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(88): Show | 92 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-221+925G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74337930 | ||||||
chr2:74337932
|
T | C | 11 | a0001c0001t0003g0260a0001c0001t0004g0264a0001c0001t0008g0258others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-221+923A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74337932 | ||||||
chr2:74337971
|
A | G | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-221+884T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74337971 | ||||||
chr2:74337982
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(2): Show | 5 | HG01192.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221+873C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74337982 | ||||||
chr2:74338059
|
A | G | 205 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(202): Show | 206 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.-221+796T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74338059 | ||||||
chr2:74338102
|
G | A | 9 | a0001c0001t0002g0174a0001c0001t0002g0176a0001c0003t0005g0175others(6): Show | 9 | HG02155.hp1 NA18941.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-221+753C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74338102 | ||||||
chr2:74338448
|
T | C | 5 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(2): Show | 5 | HG01192.hp1 HG02630.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-221+407A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74338448 | ||||||
chr2:74338644
|
C | T | 8 | a0001c0001t0002g0115a0001c0001t0008g0100a0001c0001t0011g0103others(5): Show | 8 | HG01884.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-221+211G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74338644 | ||||||
chr2:74338797
|
G | A | 1 | a0001c0001t0008g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-221+58C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 3/30 | chr2 | 74338797 | ||||||
chr2:74339011
|
G | C | 1 | a0001c0001t0008g0263 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-269-108C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74339011 | ||||||
chr2:74339058
|
C | A | 23 | a0001c0001t0001g0109a0001c0001t0001g0114a0001c0001t0002g0115others(20): Show | 23 | HG00735.hp1 HG00741.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.-269-155G>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74339058 | ||||||
chr2:74339064
|
T | C | 1 | a0001c0001t0004g0264 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-269-161A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74339064 | ||||||
chr2:74339084
|
T | C | 5 | a0001c0001t0001g0114a0001c0001t0008g0110a0001c0002t0001g0111others(2): Show | 5 | HG00741.hp1 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-269-181A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74339084 | ||||||
chr2:74339171
|
G | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(202): Show | 206 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.-269-268C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74339171 | ||||||
chr2:74339303
|
G | T | 3 | a0001c0001t0002g0014a0001c0001t0002g0015a0001c0001t0006g0013 | 3 | HG00609.hp1 NA18957.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-269-400C>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74339303 | ||||||
chr2:74339493
|
C | T | 1 | a0001c0003t0003g0012 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-269-590G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74339493 | ||||||
chr2:74339942
|
C | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(117): Show | 121 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.-269-1039G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74339942 | ||||||
chr2:74340013
|
T | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0008g0096others(1): Show | 4 | HG01192.hp1 HG02896.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-269-1110A>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74340013 | ||||||
chr2:74340050
|
A | G | 3 | a0001c0003t0003g0007a0001c0007t0004g0006a0001c0007t0004g0008 | 3 | HG03209.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-269-1147T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74340050 | ||||||
chr2:74340200
|
T | C | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-269-1297A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74340200 | ||||||
chr2:74340274
|
T | G | 1 | a0001c0001t0011g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-269-1371A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74340274 | ||||||
chr2:74340339
|
C | G | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-269-1436G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74340339 | ||||||
chr2:74340340
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(117): Show | 121 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.-269-1437T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74340340 | ||||||
chr2:74340695
|
C | T | 1 | a0001c0001t0002g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-270+1763G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74340695 | ||||||
chr2:74340760
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-270+1698G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74340760 | ||||||
chr2:74340974
|
C | T | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-270+1484G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74340974 | ||||||
chr2:74341083
|
T | C | 5 | a0001c0001t0001g0266a0001c0001t0001g0268a0001c0001t0001g0269others(2): Show | 5 | HG00280.hp1 HG01167.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-270+1375A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341083 | ||||||
chr2:74341219
|
C | T | 1 | a0001c0001t0011g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-270+1239G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341219 | ||||||
chr2:74341300
|
A | G | 1 | a0001c0001t0002g0116 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-270+1158T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341300 | ||||||
chr2:74341304
|
C | CA | 109 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(106): Show | 110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-270+1153dupT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341304 | ||||||
chr2:74341304
|
C | CAA | 6 | a0001c0001t0001g0093a0001c0001t0001g0095a0001c0001t0001g0097others(3): Show | 6 | HG01192.hp1 HG02615.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-270+1152_-270+115 others(6): Show |
SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341304 | ||||||
chr2:74341304
|
CA | C | 76 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0160others(73): Show | 76 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.-270+1153delT | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341304 | ||||||
chr2:74341430
|
A | G | 69 | a0001c0001t0001g0130a0001c0001t0001g0138a0001c0001t0001g0160others(66): Show | 69 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.-270+1028T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341430 | ||||||
chr2:74341438
|
C | T | 1 | a0001c0003t0003g0274 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-270+1020G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341438 | ||||||
chr2:74341506
|
G | C | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-270+952C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341506 | ||||||
chr2:74341766
|
G | C | 2 | a0001c0001t0002g0099a0001c0002t0001g0098 | 2 | HG02165.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-270+692C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341766 | ||||||
chr2:74341782
|
A | G | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-270+676T>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341782 | ||||||
chr2:74341889
|
C | T | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-270+569G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341889 | ||||||
chr2:74341991
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(93): Show | 97 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-270+467G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74341991 | ||||||
chr2:74342050
|
A | C | 6 | a0001c0001t0010g0278a0001c0001t0010g0279a0001c0002t0001g0005others(3): Show | 6 | HG01243.hp2 HG03098.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-270+408T>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74342050 | ||||||
chr2:74342385
|
C | T | 1 | a0001c0001t0018g0004 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-270+73G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 2/30 | chr2 | 74342385 | ||||||
chr2:74342688
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-346-154A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 1/30 | chr2 | 74342688 | ||||||
chr2:74342834
|
T | G | 1 | a0001c0001t0002g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-346-300A>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 1/30 | chr2 | 74342834 | ||||||
chr2:74342901
|
T | C | 3 | a0001c0001t0002g0275a0001c0003t0003g0274a0001c0003t0003g0276 | 3 | HG02572.hp1 HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-346-367A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 1/30 | chr2 | 74342901 | ||||||
chr2:74342906
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(116): Show | 120 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.-346-372G>A | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 1/30 | chr2 | 74342906 | ||||||
chr2:74343080
|
G | A | 1 | a0002c0004t0001g0277 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-347+276C>T | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 1/30 | chr2 | 74343080 | ||||||
chr2:74343150
|
C | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0023others(116): Show | 120 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.-347+206G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 1/30 | chr2 | 74343150 | ||||||
chr2:74343151
|
T | C | 2 | a0001c0001t0010g0278a0001c0001t0010g0279 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-347+205A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 1/30 | chr2 | 74343151 | ||||||
chr2:74343154
|
T | C | 1 | a0001c0003t0003g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-347+202A>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 1/30 | chr2 | 74343154 | ||||||
chr2:74343239
|
C | G | 1 | a0001c0001t0010g0002 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-347+117G>C | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 1/30 | chr2 | 74343239 | ||||||
chr2:74343257
|
G | C | 1 | a0003c0005t0006g0281 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-347+99C>G | SLC4A5 | ENSG00000188687.18 | transcript | ENST00000394019.7 | protein_coding | 1/30 | chr2 | 74343257 |