geneid | 54834 |
---|---|
ensemblid | ENSG00000196505.11 |
hgncid | 18010 |
symbol | GDAP2 |
name | ganglioside induced differentiation associated protein 2 |
refseq_nuc | NM_017686.4 |
refseq_prot | NP_060156.1 |
ensembl_nuc | ENST00000369443.10 |
ensembl_prot | ENSP00000358451.4 |
mane_status | MANE Select |
chr | chr1 |
start | 117863485 |
end | 117929621 |
strand | - |
ver | v1.2 |
region | chr1:117863485-117929621 |
region5000 | chr1:117858485-117934621 |
regionname0 | GDAP2_chr1_117863485_117929621 |
regionname5000 | GDAP2_chr1_117858485_117934621 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 497 | 356 | 79 | 56 | 163 | 12 | 44 | 122 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0002 | 0/0 | 497 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0003 | 0/0 | 497 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0004 | 0/0 | 497 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1494 | 335 | 60 | 54 | 163 | 12 | 44 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
c0002 | 0/0 | 1494 | 8 | 7 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
c0003 | 0/0 | 1494 | 8 | 8 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
c0004 | 0/0 | 1494 | 5 | 5 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
c0005 | 0/0 | 1494 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
c0006 | 0/0 | 1494 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
c0007 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
c0008 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 7326 | 83 | 9 | 21 | 39 | 4 | 9 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0002 | 0/0 | 7319 | 62 | 10 | 2 | 45 | 0 | 5 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0003 | 0/0 | 7324 | 39 | 10 | 12 | 8 | 3 | 6 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0004 | 0/0 | 7325 | 38 | 2 | 5 | 27 | 2 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0005 | 0/0 | 7326 | 22 | 12 | 2 | 5 | 1 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0006 | 0/0 | 7327 | 11 | 3 | 2 | 5 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0007 | 0/0 | 7326 | 10 | 0 | 0 | 10 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0008 | 0/0 | 7326 | 6 | 0 | 2 | 2 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0009 | 0/0 | 7325 | 5 | 0 | 0 | 3 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0010 | 0/0 | 7326 | 5 | 0 | 1 | 3 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0011 | 0/0 | 7325 | 5 | 5 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0012 | 0/0 | 7326 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0013 | 0/0 | 7325 | 4 | 0 | 2 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0014 | 0/0 | 7326 | 4 | 1 | 1 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0015 | 0/0 | 7326 | 4 | 0 | 0 | 4 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0016 | 0/1 | 7324 | 4 | 1 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0017 | 0/0 | 7322 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0018 | 0/0 | 7316 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0019 | 0/0 | 7326 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0020 | 0/0 | 7325 | 2 | 0 | 0 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0021 | 0/0 | 7326 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0022 | 0/0 | 7327 | 2 | 1 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0023 | 0/0 | 7324 | 2 | 0 | 0 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0024 | 0/0 | 7327 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0025 | 0/0 | 7326 | 2 | 0 | 0 | 1 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0026 | 0/0 | 7322 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0027 | 0/0 | 7322 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0028 | 0/0 | 7326 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0029 | 0/0 | 7326 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0030 | 0/0 | 7340 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0031 | 0/0 | 7319 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0032 | 0/0 | 7323 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0033 | 0/0 | 7324 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0034 | 0/0 | 7324 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0035 | 0/0 | 7324 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0036 | 0/0 | 7325 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0037 | 0/0 | 7326 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0038 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0039 | 0/0 | 7326 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0040 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0041 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0042 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0043 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0044 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0045 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0046 | 0/0 | 7327 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0047 | 0/0 | 7327 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0048 | 0/0 | 7317 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0049 | 0/0 | 7326 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0050 | 0/0 | 7327 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0051 | 0/0 | 7324 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0052 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0053 | 0/0 | 7325 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0054 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0055 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0056 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0057 | 0/0 | 7327 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0058 | 0/0 | 7326 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
t0059 | 0/0 | 7326 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 31 | 2 | 12 | 8 | 2 | 6 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0002 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0003 | 0/0 | 10 | 1 | 2 | 5 | 1 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0007 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0008 | 0/1 | 4 | 1 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0011 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0013 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0016 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0027 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1494 | 335 | 60 | 54 | 163 | 12 | 44 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0002 | 0/0 | 1494 | 8 | 7 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0003 | 0/0 | 1494 | 8 | 8 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0005 | 0/0 | 1494 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0008 | 0/0 | 1494 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0002c0004 | 0/0 | 1494 | 5 | 5 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0003c0006 | 0/0 | 1494 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0004c0007 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 8819 | 81 | 9 | 20 | 38 | 4 | 9 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0002 | 0/0 | 8812 | 54 | 3 | 1 | 45 | 0 | 5 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0003 | 0/0 | 8817 | 38 | 10 | 12 | 7 | 3 | 6 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0004 | 0/0 | 8818 | 38 | 2 | 5 | 27 | 2 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0005 | 0/0 | 8819 | 22 | 12 | 2 | 5 | 1 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0006 | 0/0 | 8820 | 10 | 3 | 2 | 4 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0007 | 0/0 | 8819 | 10 | 0 | 0 | 10 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0008 | 0/0 | 8819 | 6 | 0 | 2 | 2 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0009 | 0/0 | 8818 | 5 | 0 | 0 | 3 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0010 | 0/0 | 8819 | 5 | 0 | 1 | 3 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0013 | 0/0 | 8818 | 4 | 0 | 2 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0014 | 0/0 | 8819 | 4 | 1 | 1 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0015 | 0/0 | 8819 | 4 | 0 | 0 | 4 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0016 | 0/1 | 8817 | 4 | 1 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0018 | 0/0 | 8809 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0019 | 0/0 | 8819 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0020 | 0/0 | 8818 | 2 | 0 | 0 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0021 | 0/0 | 8819 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0022 | 0/0 | 8820 | 2 | 1 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0023 | 0/0 | 8817 | 2 | 0 | 0 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0024 | 0/0 | 8820 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0025 | 0/0 | 8819 | 2 | 0 | 0 | 1 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0028 | 0/0 | 8819 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0029 | 0/0 | 8819 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0030 | 0/0 | 8833 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0031 | 0/0 | 8812 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0032 | 0/0 | 8816 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0033 | 0/0 | 8817 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0034 | 0/0 | 8817 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0035 | 0/0 | 8817 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0036 | 0/0 | 8818 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0037 | 0/0 | 8819 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0038 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0039 | 0/0 | 8819 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0040 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0041 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0042 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0043 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0044 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0045 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0046 | 0/0 | 8820 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0047 | 0/0 | 8820 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0048 | 0/0 | 8810 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0049 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0050 | 0/0 | 8820 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0051 | 0/0 | 8817 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0052 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0053 | 0/0 | 8818 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0054 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0055 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0056 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0057 | 0/0 | 8820 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0058 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0001t0059 | 0/0 | 8819 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0002t0002 | 0/0 | 8812 | 8 | 7 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0003t0017 | 0/0 | 8815 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0003t0026 | 0/0 | 8815 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0003t0027 | 0/0 | 8815 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0005t0012 | 0/0 | 8819 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0001c0008t0001 | 0/0 | 8819 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0002c0004t0011 | 0/0 | 8818 | 5 | 5 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0003c0006t0001 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0003c0006t0006 | 0/0 | 8820 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
a0004c0007t0003 | 0/0 | 8817 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | copy fasta | chr1 | 117858485 | 117934621 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 31 | 2 | 12 | 8 | 2 | 6 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0013 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0002 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0003 | 0/0 | 10 | 1 | 2 | 5 | 1 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0006g0011 | 0/0 | 4 | 1 | 2 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0007g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0008g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0008g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0009g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0009g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0009g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0009g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0010g0016 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0010g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0010g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0013g0007 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0014g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0014g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0014g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0014g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0015g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0015g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0016g0008 | 0/1 | 4 | 1 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0018g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0018g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0019g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0019g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0020g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0020g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0021g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0022g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0022g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0023g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0023g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0024g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0025g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0025g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0028g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0029g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0030g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0031g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0032g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0033g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0034g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0035g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0036g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0037g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0038g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0039g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0040g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0041g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0042g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0043g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0044g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0045g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0046g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0047g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0048g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0049g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0050g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0051g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0052g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0053g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0054g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0055g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0056g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0057g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0058g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0001t0059g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0002t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0002t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0003t0017g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0003t0017g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0003t0017g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0003t0017g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0003t0026g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0003t0026g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0003t0027g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0005t0012g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0005t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0005t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0001c0008t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0002c0004t0011g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0002c0004t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0002c0004t0011g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0003c0006t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0003c0006t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
a0004c0007t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0004 | g0030 | EUR | GBR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0219 | EUR | GBR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0027 | EUR | FIN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0003 | EUR | FIN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00323 | hp2 | a0001 | c0001 | t0028 | g0049 | EUR | FIN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00423 | hp2 | a0001 | c0001 | t0010 | g0099 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00438 | hp2 | a0003 | c0006 | t0001 | g0222 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00621 | hp1 | a0001 | c0001 | t0015 | g0043 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00673 | hp2 | a0001 | c0001 | t0031 | g0202 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00733 | hp2 | a0001 | c0001 | t0013 | g0007 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00735 | hp1 | a0001 | c0001 | t0010 | g0016 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00735 | hp2 | a0001 | c0001 | t0039 | g0155 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0173 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01109 | hp2 | a0001 | c0001 | t0046 | g0124 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01175 | hp2 | a0001 | c0001 | t0029 | g0113 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01255 | hp1 | a0001 | c0001 | t0014 | g0085 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0011 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0068 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01346 | hp2 | a0001 | c0001 | t0013 | g0007 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01361 | hp1 | a0001 | c0001 | t0016 | g0008 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0047 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0189 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0067 | EUR | IBS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01517 | hp1 | a0001 | c0001 | t0032 | g0066 | EUR | IBS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01884 | hp1 | a0001 | c0001 | t0016 | g0008 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01884 | hp2 | a0001 | c0001 | t0021 | g0040 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01928 | hp2 | a0001 | c0008 | t0001 | g0114 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01975 | hp1 | a0001 | c0001 | t0008 | g0024 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01975 | hp2 | a0001 | c0001 | t0033 | g0105 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01981 | hp1 | a0001 | c0001 | t0006 | g0011 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02027 | hp1 | a0001 | c0001 | t0015 | g0043 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02040 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0187 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02080 | hp2 | a0001 | c0001 | t0006 | g0137 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02083 | hp2 | a0001 | c0001 | t0015 | g0042 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02129 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02135 | hp2 | a0001 | c0001 | t0035 | g0058 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0153 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | CDX | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02257 | hp2 | a0001 | c0001 | t0057 | g0180 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02258 | hp1 | a0001 | c0001 | t0024 | g0023 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02258 | hp2 | a0001 | c0003 | t0017 | g0229 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02273 | hp1 | a0001 | c0001 | t0008 | g0024 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02280 | hp2 | a0002 | c0004 | t0011 | g0022 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02300 | hp1 | a0001 | c0001 | t0016 | g0008 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02451 | hp1 | a0001 | c0001 | t0018 | g0061 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02523 | hp1 | a0001 | c0001 | t0040 | g0135 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02622 | hp1 | a0001 | c0005 | t0012 | g0059 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02622 | hp2 | a0001 | c0003 | t0017 | g0233 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0170 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02630 | hp2 | a0001 | c0001 | t0036 | g0214 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0186 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02683 | hp1 | a0001 | c0001 | t0009 | g0132 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02683 | hp2 | a0001 | c0001 | t0023 | g0086 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02698 | hp1 | a0001 | c0001 | t0010 | g0016 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02698 | hp2 | a0001 | c0001 | t0025 | g0051 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02723 | hp1 | a0001 | c0001 | t0018 | g0026 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02735 | hp1 | a0001 | c0001 | t0034 | g0065 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02735 | hp2 | a0001 | c0001 | t0014 | g0134 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0169 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02809 | hp2 | a0001 | c0001 | t0047 | g0191 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02818 | hp2 | a0001 | c0003 | t0027 | g0048 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0188 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02897 | hp2 | a0001 | c0001 | t0053 | g0226 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02922 | hp1 | a0001 | c0001 | t0021 | g0040 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02965 | hp1 | a0001 | c0001 | t0024 | g0023 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02965 | hp2 | a0001 | c0001 | t0055 | g0175 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02976 | hp1 | a0001 | c0001 | t0058 | g0168 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02976 | hp2 | a0001 | c0003 | t0026 | g0231 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03017 | hp1 | a0001 | c0001 | t0023 | g0077 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03041 | hp1 | a0001 | c0001 | t0052 | g0172 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0190 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03130 | hp1 | a0001 | c0001 | t0056 | g0176 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03195 | hp1 | a0001 | c0001 | t0005 | g0181 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03195 | hp2 | a0001 | c0005 | t0012 | g0060 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03209 | hp1 | a0001 | c0001 | t0054 | g0177 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0075 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03225 | hp2 | a0001 | c0003 | t0027 | g0048 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0220 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03239 | hp2 | a0001 | c0001 | t0020 | g0098 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03453 | hp1 | a0001 | c0001 | t0048 | g0063 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03486 | hp1 | a0001 | c0003 | t0017 | g0230 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03486 | hp2 | a0001 | c0001 | t0018 | g0026 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03490 | hp1 | a0001 | c0001 | t0013 | g0007 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0162 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0055 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03491 | hp2 | a0001 | c0001 | t0009 | g0133 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03492 | hp2 | a0001 | c0001 | t0013 | g0007 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03516 | hp1 | a0001 | c0001 | t0014 | g0129 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03516 | hp2 | a0002 | c0004 | t0011 | g0217 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03540 | hp1 | a0001 | c0005 | t0012 | g0025 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03540 | hp2 | a0001 | c0003 | t0026 | g0234 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03579 | hp1 | a0001 | c0005 | t0012 | g0025 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03579 | hp2 | a0001 | c0001 | t0038 | g0057 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03704 | hp1 | a0001 | c0001 | t0020 | g0110 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03834 | hp1 | a0001 | c0001 | t0008 | g0054 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03927 | hp1 | a0001 | c0001 | t0022 | g0218 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0109 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0047 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG04115 | hp2 | a0001 | c0001 | t0059 | g0052 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG04184 | hp1 | a0001 | c0001 | t0014 | g0161 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG04184 | hp2 | a0001 | c0001 | t0051 | g0108 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0103 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG04204 | hp2 | a0001 | c0001 | t0037 | g0130 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18522 | hp2 | a0002 | c0004 | t0011 | g0216 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CHB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18940 | hp1 | a0003 | c0006 | t0006 | g0221 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18941 | hp2 | a0001 | c0001 | t0007 | g0160 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18944 | hp2 | a0001 | c0001 | t0019 | g0039 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18945 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18946 | hp2 | a0001 | c0001 | t0005 | g0182 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18948 | hp2 | a0001 | c0001 | t0009 | g0165 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18949 | hp1 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18951 | hp1 | a0001 | c0001 | t0009 | g0120 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18957 | hp1 | a0001 | c0001 | t0041 | g0146 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18962 | hp1 | a0001 | c0001 | t0025 | g0050 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18964 | hp2 | a0001 | c0001 | t0015 | g0042 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18966 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18967 | hp2 | a0001 | c0001 | t0049 | g0092 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18973 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18974 | hp1 | a0001 | c0001 | t0007 | g0118 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18977 | hp1 | a0001 | c0001 | t0042 | g0121 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18978 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18984 | hp1 | a0001 | c0001 | t0019 | g0167 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18985 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18985 | hp2 | a0001 | c0001 | t0007 | g0157 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18986 | hp1 | a0001 | c0001 | t0010 | g0016 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18988 | hp1 | a0001 | c0001 | t0019 | g0039 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18989 | hp1 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19000 | hp2 | a0001 | c0001 | t0050 | g0158 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19004 | hp1 | a0001 | c0001 | t0045 | g0127 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19005 | hp2 | a0001 | c0001 | t0007 | g0159 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19010 | hp2 | a0001 | c0001 | t0009 | g0131 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19011 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19012 | hp1 | a0001 | c0001 | t0044 | g0091 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19012 | hp2 | a0001 | c0001 | t0008 | g0053 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0171 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19043 | hp2 | a0001 | c0003 | t0017 | g0232 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19056 | hp1 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19057 | hp1 | a0001 | c0001 | t0010 | g0080 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19058 | hp1 | a0004 | c0007 | t0003 | g0089 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19059 | hp1 | a0001 | c0001 | t0030 | g0185 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19059 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19074 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19074 | hp2 | a0001 | c0001 | t0008 | g0056 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19080 | hp1 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19082 | hp1 | a0001 | c0001 | t0043 | g0144 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19087 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ASW | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | ASW | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0083 | EUR | TSI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | GIH | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | GIH | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02486 | hp1 | a0001 | c0001 | t0022 | g0174 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02486 | hp2 | a0002 | c0004 | t0011 | g0022 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02559 | hp1 | a0002 | c0004 | t0011 | g0022 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0115 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | USA | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | USA | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA18955 | hp2 | a0001 | c0001 | t0007 | g0163 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | USA | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0016 | g0008 | REF | REF | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117870598
|
T | C | 1 | a0002 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
missense_variant | MODERATE | c.1465A>G | p.Thr489Ala | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1706/8819 | 1465/1494 | 489/497 | chr1 | 117870598 | ||
chr1:117883525
|
C | T | 1 | a0004 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.1210G>A | p.Asp404Asn | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/14 | 1451/8819 | 1210/1494 | 404/497 | chr1 | 117883525 | ||
chr1:117899149
|
G | A | 1 | a0003 | 2 | HG00438.hp2 NA18940.hp1 |
missense_variant | MODERATE | c.704C>T | p.Pro235Leu | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/14 | 945/8819 | 704/1494 | 235/497 | chr1 | 117899149 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117886592
|
T | C | 1 | a0001c0008 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1092A>G | p.Leu364Leu | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/14 | 1333/8819 | 1092/1494 | 364/497 | chr1 | 117886592 | ||
chr1:117906581
|
G | C | 1 | a0001c0003 | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.561C>G | p.Arg187Arg | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/14 | 802/8819 | 561/1494 | 187/497 | chr1 | 117906581 | ||
chr1:117918649
|
A | G | 1 | a0001c0002 | 8 | HG01433.hp1 HG02055.hp2 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.264T>C | p.Ser88Ser | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/14 | 505/8819 | 264/1494 | 88/497 | chr1 | 117918649 | ||
chr1:117920292
|
T | C | 1 | a0001c0005 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
synonymous_variant | LOW | c.66A>G | p.Ser22Ser | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/14 | 307/8819 | 66/1494 | 22/497 | chr1 | 117920292 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117863575
|
A | G | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6994T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6994 | chr1 | 117863575 | |||||
chr1:117863586
|
A | C | 4 | a0001c0001t0014a0001c0001t0037a0001c0001t0039others(1): Show | 7 | HG00735.hp2 HG01109.hp2 HG01255.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6983T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6983 | chr1 | 117863586 | |||||
chr1:117863644
|
TTGAGAAA others(3): Show |
T | 2 | a0001c0001t0018a0001c0001t0048 | 4 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6915_*6924delTATT others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6915 | chr1 | 117863644 | |||||
chr1:117863845
|
T | A | 1 | a0001c0001t0039 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6724A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6724 | chr1 | 117863845 | |||||
chr1:117864046
|
T | C | 1 | a0001c0001t0021 | 2 | HG01884.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6523A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6523 | chr1 | 117864046 | |||||
chr1:117864078
|
A | G | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6491T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6491 | chr1 | 117864078 | |||||
chr1:117864224
|
T | C | 2 | a0001c0001t0015a0001c0001t0047 | 5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6345A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6345 | chr1 | 117864224 | |||||
chr1:117864416
|
G | A | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6153C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6153 | chr1 | 117864416 | |||||
chr1:117864433
|
G | C | 1 | a0001c0001t0038 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6136C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6136 | chr1 | 117864433 | |||||
chr1:117864438
|
T | A | 2 | a0001c0001t0018a0001c0001t0048 | 4 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6131A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6131 | chr1 | 117864438 | |||||
chr1:117864451
|
G | A | 1 | a0001c0001t0036 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6118C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6118 | chr1 | 117864451 | |||||
chr1:117864729
|
A | G | 1 | a0001c0001t0051 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5840T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5840 | chr1 | 117864729 | |||||
chr1:117864825
|
G | A | 1 | a0001c0001t0044 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5744C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5744 | chr1 | 117864825 | |||||
chr1:117864878
|
C | T | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5691G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5691 | chr1 | 117864878 | |||||
chr1:117864886
|
G | T | 1 | a0001c0001t0035 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5683C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5683 | chr1 | 117864886 | |||||
chr1:117864922
|
C | T | 11 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(8): Show | 27 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5647G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5647 | chr1 | 117864922 | |||||
chr1:117865004
|
A | G | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5565T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5565 | chr1 | 117865004 | |||||
chr1:117865051
|
C | T | 1 | a0001c0001t0038 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5518G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5518 | chr1 | 117865051 | |||||
chr1:117865167
|
T | C | 3 | a0001c0003t0017a0001c0003t0026a0001c0003t0027 | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5402A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5402 | chr1 | 117865167 | |||||
chr1:117865270
|
T | TCATCCTG others(7): Show |
1 | a0001c0001t0030 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5298_*5299insGAAC others(10): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5298 | chr1 | 117865270 | |||||
chr1:117865324
|
G | C | 1 | a0001c0001t0040 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5245C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5245 | chr1 | 117865324 | |||||
chr1:117865427
|
C | A | 1 | a0001c0001t0041 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5142G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5142 | chr1 | 117865427 | |||||
chr1:117865554
|
C | T | 1 | a0001c0001t0055 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5015G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5015 | chr1 | 117865554 | |||||
chr1:117865597
|
A | C | 1 | a0001c0001t0054 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4972T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4972 | chr1 | 117865597 | |||||
chr1:117865599
|
A | G | 1 | a0001c0001t0034 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4970T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4970 | chr1 | 117865599 | |||||
chr1:117865653
|
A | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4916T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4916 | chr1 | 117865653 | |||||
chr1:117865702
|
A | T | 1 | a0001c0001t0031 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4867T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4867 | chr1 | 117865702 | |||||
chr1:117865736
|
G | A | 1 | a0001c0003t0017 | 4 | HG02258.hp2 HG02622.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4833C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4833 | chr1 | 117865736 | |||||
chr1:117865835
|
T | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4734A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4734 | chr1 | 117865835 | |||||
chr1:117865887
|
A | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4682T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4682 | chr1 | 117865887 | |||||
chr1:117865988
|
T | C | 1 | a0001c0001t0042 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4581A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4581 | chr1 | 117865988 | |||||
chr1:117866010
|
T | C | 1 | a0001c0005t0012 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4559A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4559 | chr1 | 117866010 | |||||
chr1:117866090
|
C | T | 2 | a0001c0001t0013a0001c0001t0020 | 6 | HG00733.hp2 HG01346.hp2 HG03239.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4479G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4479 | chr1 | 117866090 | |||||
chr1:117866107
|
G | A | 1 | a0001c0001t0020 | 2 | HG03239.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4462C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4462 | chr1 | 117866107 | |||||
chr1:117866157
|
G | C | 1 | a0001c0001t0043 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4412C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4412 | chr1 | 117866157 | |||||
chr1:117866433
|
C | T | 1 | a0001c0001t0057 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4136G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4136 | chr1 | 117866433 | |||||
chr1:117866437
|
CT | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4131delA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4131 | chr1 | 117866437 | |||||
chr1:117866456
|
T | C | 3 | a0001c0001t0029a0001c0001t0052a0001c0001t0058 | 3 | HG01175.hp2 HG02976.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4113A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4113 | chr1 | 117866456 | |||||
chr1:117866541
|
T | C | 2 | a0001c0001t0018a0001c0001t0048 | 4 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4028A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4028 | chr1 | 117866541 | |||||
chr1:117866616
|
A | G | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3953T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3953 | chr1 | 117866616 | |||||
chr1:117866621
|
A | G | 1 | a0001c0001t0033 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3948T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3948 | chr1 | 117866621 | |||||
chr1:117866624
|
T | C | 15 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(12): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3945A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3945 | chr1 | 117866624 | |||||
chr1:117866880
|
AG | A | 2 | a0001c0001t0008a0001c0001t0025 | 8 | HG01975.hp1 HG02273.hp1 HG02698.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3688delC | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3688 | chr1 | 117866880 | |||||
chr1:117866881
|
G | A | 5 | a0001c0001t0024a0001c0001t0059a0001c0003t0017others(2): Show | 11 | HG02258.hp1 HG02258.hp2 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3688C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3688 | chr1 | 117866881 | |||||
chr1:117867024
|
T | A | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3545A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3545 | chr1 | 117867024 | |||||
chr1:117867059
|
T | C | 1 | a0001c0001t0045 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3510A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3510 | chr1 | 117867059 | |||||
chr1:117867070
|
T | A | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3499A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3499 | chr1 | 117867070 | |||||
chr1:117867214
|
A | G | 1 | a0001c0001t0037 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3355T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3355 | chr1 | 117867214 | |||||
chr1:117867411
|
G | A | 2 | a0001c0001t0055a0001c0001t0056 | 2 | HG02965.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3158C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3158 | chr1 | 117867411 | |||||
chr1:117867463
|
A | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3106T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3106 | chr1 | 117867463 | |||||
chr1:117867527
|
G | GA | 8 | a0001c0001t0006a0001c0001t0022a0001c0001t0046others(5): Show | 18 | HG01109.hp2 HG01255.hp2 HG01981.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3041dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3041 | chr1 | 117867527 | |||||
chr1:117867527
|
GA | G | 7 | a0001c0001t0004a0001c0001t0009a0001c0001t0013others(4): Show | 56 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*3041delT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3041 | chr1 | 117867527 | |||||
chr1:117867527
|
GAA | G | 8 | a0001c0001t0003a0001c0001t0016a0001c0001t0023others(5): Show | 49 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3040_*3041delTT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3040 | chr1 | 117867527 | |||||
chr1:117867527
|
GAAA | G | 4 | a0001c0001t0032a0001c0003t0017a0001c0003t0026others(1): Show | 9 | HG01517.hp1 HG02258.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3039_*3041delTTT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3039 | chr1 | 117867527 | |||||
chr1:117867527
|
GAAAAAAA | G | 3 | a0001c0001t0002a0001c0001t0031a0001c0002t0002 | 63 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3035_*3041delTTTT others(3): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3035 | chr1 | 117867527 | |||||
chr1:117867543
|
A | AT | 3 | a0001c0001t0008a0001c0001t0024a0001c0001t0025 | 10 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3025_*3026insA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3025 | chr1 | 117867543 | |||||
chr1:117867546
|
A | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3023T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3023 | chr1 | 117867546 | |||||
chr1:117867648
|
G | A | 1 | a0001c0001t0049 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2921C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2921 | chr1 | 117867648 | |||||
chr1:117867663
|
T | C | 2 | a0001c0001t0007a0001c0001t0050 | 11 | NA18941.hp2 NA18949.hp1 NA18955.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2906A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2906 | chr1 | 117867663 | |||||
chr1:117867688
|
T | C | 7 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(4): Show | 19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2881A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2881 | chr1 | 117867688 | |||||
chr1:117867700
|
CA | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2868delT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2868 | chr1 | 117867700 | |||||
chr1:117867754
|
A | G | 1 | a0002c0004t0011 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2815T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2815 | chr1 | 117867754 | |||||
chr1:117868416
|
A | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2153T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2153 | chr1 | 117868416 | |||||
chr1:117868435
|
T | G | 2 | a0001c0001t0016a0001c0001t0051 | 5 | HG01361.hp1 HG01884.hp1 HG02300.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2134A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2134 | chr1 | 117868435 | |||||
chr1:117868437
|
T | A | 1 | a0001c0001t0030 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2132A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2132 | chr1 | 117868437 | |||||
chr1:117868525
|
C | T | 1 | a0002c0004t0011 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2044G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2044 | chr1 | 117868525 | |||||
chr1:117868537
|
T | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2032A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2032 | chr1 | 117868537 | |||||
chr1:117868613
|
C | G | 2 | a0001c0001t0052a0001c0001t0058 | 2 | HG02976.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1956G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1956 | chr1 | 117868613 | |||||
chr1:117868752
|
A | AC | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1816_*1817insG | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1816 | chr1 | 117868752 | |||||
chr1:117868761
|
G | A | 7 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(4): Show | 19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1808C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1808 | chr1 | 117868761 | |||||
chr1:117868865
|
G | A | 1 | a0001c0001t0025 | 2 | HG02698.hp2 NA18962.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1704C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1704 | chr1 | 117868865 | |||||
chr1:117868893
|
T | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1676A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1676 | chr1 | 117868893 | |||||
chr1:117868945
|
T | C | 11 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(8): Show | 27 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1624A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1624 | chr1 | 117868945 | |||||
chr1:117868961
|
G | A | 3 | a0001c0003t0017a0001c0003t0026a0001c0003t0027 | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1608C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1608 | chr1 | 117868961 | |||||
chr1:117868985
|
C | CA | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1583dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1583 | chr1 | 117868985 | |||||
chr1:117869023
|
A | T | 1 | a0001c0001t0030 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1546T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1546 | chr1 | 117869023 | |||||
chr1:117869176
|
T | C | 9 | a0001c0001t0005a0001c0001t0021a0001c0001t0022others(6): Show | 32 | HG00140.hp2 HG00741.hp1 HG01361.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1393A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1393 | chr1 | 117869176 | |||||
chr1:117869210
|
CA | C | 3 | a0001c0003t0017a0001c0003t0026a0001c0003t0027 | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1358delT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1358 | chr1 | 117869210 | |||||
chr1:117869708
|
T | C | 1 | a0001c0003t0027 | 2 | HG02818.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*861A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 861 | chr1 | 117869708 | |||||
chr1:117869745
|
T | C | 1 | a0001c0001t0023 | 2 | HG02683.hp2 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*824A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 824 | chr1 | 117869745 | |||||
chr1:117869901
|
A | C | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*668T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 668 | chr1 | 117869901 | |||||
chr1:117869942
|
G | A | 4 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(1): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*627C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 627 | chr1 | 117869942 | |||||
chr1:117870109
|
A | G | 1 | a0001c0005t0012 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*460T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 460 | chr1 | 117870109 | |||||
chr1:117870232
|
T | C | 1 | a0001c0001t0019 | 3 | NA18944.hp2 NA18984.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*337A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 337 | chr1 | 117870232 | |||||
chr1:117870238
|
C | G | 3 | a0001c0003t0017a0001c0003t0026a0001c0003t0027 | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*331G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 331 | chr1 | 117870238 | |||||
chr1:117920387
|
A | C | 1 | a0001c0001t0029 | 1 | HG01175.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-30T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/14 | chr1 | 117920387 | ||||||
chr1:117929583
|
T | C | 3 | a0001c0003t0017a0001c0003t0026a0001c0003t0027 | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-203A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/14 | 9226 | chr1 | 117929583 | |||||
chr1:117929587
|
C | T | 1 | a0001c0001t0028 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-207G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/14 | 9230 | chr1 | 117929587 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:117870687
|
G | T | 1 | a0001c0001t0009g0132 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1447-71C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117870687 | ||||||
chr1:117870793
|
C | T | 1 | a0001c0003t0027g0048 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1447-177G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117870793 | ||||||
chr1:117870846
|
A | C | 3 | a0001c0001t0029g0113a0001c0001t0052g0172a0001c0001t0058g0168 | 3 | HG01175.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1447-230T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117870846 | ||||||
chr1:117870934
|
C | T | 1 | a0001c0001t0002g0193 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1447-318G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117870934 | ||||||
chr1:117871040
|
T | C | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-424A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871040 | ||||||
chr1:117871238
|
G | A | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-622C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871238 | ||||||
chr1:117871333
|
T | C | 1 | a0001c0001t0035g0058 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1447-717A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871333 | ||||||
chr1:117871459
|
A | C | 3 | a0001c0001t0015g0042a0001c0001t0015g0043a0001c0001t0047g0191 | 5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447-843T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871459 | ||||||
chr1:117871557
|
CTACAGAG others(6): Show |
C | 1 | a0001c0001t0030g0185 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1447-954_1447-942d others(15): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871557 | ||||||
chr1:117871753
|
T | TA | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-1138dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871753 | ||||||
chr1:117871781
|
G | C | 1 | a0001c0001t0001g0037 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1447-1165C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871781 | ||||||
chr1:117871824
|
C | CT | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-1209dupA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871824 | ||||||
chr1:117871982
|
A | T | 133 | a0001c0001t0001g0062a0001c0001t0001g0195a0001c0001t0001g0212others(130): Show | 204 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.1447-1366T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871982 | ||||||
chr1:117872147
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-1531G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872147 | ||||||
chr1:117872375
|
A | G | 2 | a0001c0001t0003g0084a0001c0001t0003g0095 | 2 | HG01243.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1447-1759T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872375 | ||||||
chr1:117872546
|
C | G | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1447-1930G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872546 | ||||||
chr1:117872547
|
G | A | 8 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(5): Show | 9 | HG01975.hp1 HG02273.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1447-1931C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872547 | ||||||
chr1:117872650
|
T | C | 1 | a0001c0001t0059g0052 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1447-2034A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872650 | ||||||
chr1:117872807
|
T | C | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1447-2191A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872807 | ||||||
chr1:117873022
|
A | T | 1 | a0001c0001t0047g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1447-2406T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873022 | ||||||
chr1:117873126
|
A | G | 2 | a0001c0001t0002g0004a0001c0001t0030g0185 | 7 | HG00438.hp1 HG00558.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1447-2510T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873126 | ||||||
chr1:117873277
|
G | C | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1447-2661C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873277 | ||||||
chr1:117873320
|
C | T | 1 | a0001c0001t0047g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1447-2704G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873320 | ||||||
chr1:117873350
|
T | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-2734A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873350 | ||||||
chr1:117873822
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1447-3206A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873822 | ||||||
chr1:117873823
|
C | T | 1 | a0001c0001t0024g0023 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1447-3207G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873823 | ||||||
chr1:117874055
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0143a0001c0001t0009g0131 | 4 | NA18954.hp2 NA18983.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447-3439T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874055 | ||||||
chr1:117874084
|
G | A | 1 | a0001c0001t0036g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1447-3468C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874084 | ||||||
chr1:117874101
|
A | G | 3 | a0001c0001t0018g0026a0001c0001t0018g0061a0001c0001t0048g0063 | 4 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-3485T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874101 | ||||||
chr1:117874103
|
C | T | 2 | a0001c0001t0018g0026a0001c0001t0048g0063 | 3 | HG02723.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1447-3487G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874103 | ||||||
chr1:117874225
|
G | A | 1 | a0001c0001t0046g0124 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1447-3609C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874225 | ||||||
chr1:117874414
|
G | A | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+3595C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874414 | ||||||
chr1:117874634
|
T | G | 1 | a0001c0001t0008g0024 | 2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1446+3375A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874634 | ||||||
chr1:117874682
|
A | G | 1 | a0001c0001t0020g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1446+3327T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874682 | ||||||
chr1:117874861
|
A | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+3148T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874861 | ||||||
chr1:117874920
|
C | T | 64 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(61): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1446+3089G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874920 | ||||||
chr1:117875190
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0184 | 2 | NA19064.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1446+2819C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875190 | ||||||
chr1:117875234
|
C | T | 1 | a0001c0001t0059g0052 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1446+2775G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875234 | ||||||
chr1:117875269
|
G | A | 8 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(5): Show | 9 | HG01975.hp1 HG02273.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1446+2740C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875269 | ||||||
chr1:117875354
|
G | C | 4 | a0001c0001t0001g0138a0001c0001t0001g0166a0001c0001t0006g0137others(1): Show | 4 | HG00597.hp2 HG02080.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.1446+2655C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875354 | ||||||
chr1:117875521
|
C | T | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+2488G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875521 | ||||||
chr1:117875659
|
G | A | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+2350C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875659 | ||||||
chr1:117875866
|
C | A | 3 | a0001c0001t0014g0129a0001c0001t0014g0161a0001c0001t0046g0124 | 3 | HG01109.hp2 HG03516.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1446+2143G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875866 | ||||||
chr1:117876145
|
G | A | 3 | a0001c0001t0004g0032a0001c0001t0004g0082a0001c0001t0004g0094 | 4 | NA18950.hp1 NA18954.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+1864C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117876145 | ||||||
chr1:117876317
|
T | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+1692A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117876317 | ||||||
chr1:117876620
|
T | C | 1 | a0001c0001t0038g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1446+1389A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117876620 | ||||||
chr1:117876844
|
A | G | 1 | a0001c0001t0003g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1446+1165T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117876844 | ||||||
chr1:117876875
|
A | G | 2 | a0001c0001t0052g0172a0001c0001t0058g0168 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1446+1134T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117876875 | ||||||
chr1:117877021
|
T | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+988A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877021 | ||||||
chr1:117877467
|
C | T | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1446+542G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877467 | ||||||
chr1:117877677
|
G | A | 2 | a0001c0001t0002g0041a0001c0001t0002g0178 | 3 | HG02451.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1446+332C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877677 | ||||||
chr1:117877711
|
A | G | 1 | a0001c0001t0015g0042 | 2 | HG02083.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1446+298T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877711 | ||||||
chr1:117877715
|
G | T | 1 | a0001c0001t0001g0195 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1446+294C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877715 | ||||||
chr1:117877830
|
C | G | 64 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(61): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1446+179G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877830 | ||||||
chr1:117877844
|
A | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+165T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877844 | ||||||
chr1:117877924
|
G | A | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+85C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877924 | ||||||
chr1:117878161
|
T | C | 1 | a0001c0001t0006g0141 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1303-9A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117878161 | ||||||
chr1:117878162
|
A | G | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1303-10T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117878162 | ||||||
chr1:117878487
|
C | T | 65 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(62): Show | 99 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1303-335G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117878487 | ||||||
chr1:117878508
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0002g0193 | 2 | HG00597.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1303-356A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117878508 | ||||||
chr1:117878922
|
G | A | 1 | a0001c0003t0027g0048 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1303-770C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117878922 | ||||||
chr1:117879039
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1303-887C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879039 | ||||||
chr1:117879080
|
T | C | 1 | a0001c0001t0006g0140 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1303-928A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879080 | ||||||
chr1:117879378
|
G | T | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1303-1226C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879378 | ||||||
chr1:117879405
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0006g0141a0001c0001t0043g0144 | 4 | NA18971.hp1 NA19066.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1303-1253A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879405 | ||||||
chr1:117879950
|
G | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1303-1798C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879950 | ||||||
chr1:117879997
|
G | A | 3 | a0001c0001t0005g0018a0001c0001t0005g0169a0001c0001t0005g0170 | 5 | HG02630.hp1 HG02809.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+1826C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879997 | ||||||
chr1:117880069
|
T | C | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1302+1754A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880069 | ||||||
chr1:117880091
|
G | A | 2 | a0001c0001t0003g0067a0001c0001t0032g0066 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1302+1732C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880091 | ||||||
chr1:117880229
|
T | G | 1 | a0001c0001t0024g0023 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1302+1594A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880229 | ||||||
chr1:117880261
|
C | T | 1 | a0001c0003t0027g0048 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1302+1562G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880261 | ||||||
chr1:117880333
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+1490G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880333 | ||||||
chr1:117880365
|
T | C | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+1458A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880365 | ||||||
chr1:117880564
|
T | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0164 | 2 | NA19063.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1302+1259A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880564 | ||||||
chr1:117880758
|
C | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+1065G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880758 | ||||||
chr1:117880929
|
C | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+894G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880929 | ||||||
chr1:117880997
|
A | T | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+826T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880997 | ||||||
chr1:117881461
|
G | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+362C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117881461 | ||||||
chr1:117881647
|
C | T | 65 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(62): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1302+176G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117881647 | ||||||
chr1:117881942
|
A | T | 1 | a0001c0001t0001g0228 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1248-65T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117881942 | ||||||
chr1:117881945
|
G | C | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248-68C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117881945 | ||||||
chr1:117881949
|
A | G | 1 | a0003c0006t0001g0222 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1248-72T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117881949 | ||||||
chr1:117881996
|
A | G | 20 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(17): Show | 25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1248-119T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117881996 | ||||||
chr1:117882073
|
C | G | 20 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(17): Show | 25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1248-196G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882073 | ||||||
chr1:117882307
|
A | G | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1248-430T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882307 | ||||||
chr1:117882453
|
C | G | 1 | a0001c0001t0001g0145 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1248-576G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882453 | ||||||
chr1:117882671
|
T | C | 1 | a0001c0001t0038g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1248-794A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882671 | ||||||
chr1:117882693
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1247+795G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882693 | ||||||
chr1:117882712
|
C | G | 130 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(127): Show | 200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1247+776G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882712 | ||||||
chr1:117882865
|
G | C | 2 | a0001c0001t0003g0106a0001c0001t0003g0107 | 2 | HG03654.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1247+623C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882865 | ||||||
chr1:117883041
|
T | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1247+447A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117883041 | ||||||
chr1:117883217
|
GT | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1247+270delA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117883217 | ||||||
chr1:117883379
|
T | G | 3 | a0001c0001t0015g0042a0001c0001t0015g0043a0001c0001t0047g0191 | 5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1247+109A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117883379 | ||||||
chr1:117883718
|
G | T | 1 | a0001c0001t0014g0161 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1108-91C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117883718 | ||||||
chr1:117883775
|
T | C | 64 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(61): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1108-148A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117883775 | ||||||
chr1:117883865
|
C | T | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1108-238G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117883865 | ||||||
chr1:117883868
|
A | T | 1 | a0001c0001t0008g0024 | 2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1108-241T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117883868 | ||||||
chr1:117883980
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1108-353A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117883980 | ||||||
chr1:117884005
|
T | C | 1 | a0001c0001t0057g0180 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1108-378A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884005 | ||||||
chr1:117884199
|
C | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1108-572G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884199 | ||||||
chr1:117884387
|
G | A | 1 | a0001c0005t0012g0025 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1108-760C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884387 | ||||||
chr1:117884401
|
A | G | 2 | a0001c0001t0004g0015a0001c0001t0004g0101 | 4 | NA18945.hp2 NA18966.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108-774T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884401 | ||||||
chr1:117884420
|
C | T | 1 | a0001c0001t0004g0081 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1108-793G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884420 | ||||||
chr1:117884704
|
T | A | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1108-1077A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884704 | ||||||
chr1:117884813
|
C | CAT | 5 | a0001c0001t0001g0116a0001c0001t0003g0028a0001c0001t0004g0093others(2): Show | 6 | HG02132.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1108-1187_1108-118 others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
C | CATGT | 7 | a0001c0001t0001g0062a0001c0001t0002g0178a0001c0001t0015g0043others(4): Show | 10 | HG00621.hp1 HG02027.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1108-1187_1108-118 others(8): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
C | CATGTGT | 59 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(56): Show | 94 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1108-1187_1108-118 others(10): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
C | CATGTGTG others(1): Show |
5 | a0001c0001t0003g0083a0001c0001t0004g0031a0001c0001t0004g0096others(2): Show | 6 | HG02155.hp2 HG02451.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1108-1187_1108-118 others(12): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
C | CATGTGTG others(3): Show |
2 | a0001c0001t0004g0030a0001c0001t0004g0068 | 3 | HG00140.hp1 HG00738.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1108-1187_1108-118 others(14): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
C | CGT | 10 | a0001c0001t0001g0117a0001c0001t0002g0208a0001c0001t0005g0047others(7): Show | 11 | HG00140.hp2 HG00741.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1108-1188_1108-118 others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
C | CGTGT | 11 | a0001c0001t0002g0004a0001c0001t0002g0200a0001c0001t0003g0064others(8): Show | 17 | HG00438.hp1 HG00558.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1108-1190_1108-118 others(8): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
C | CGTGTGT | 25 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(22): Show | 42 | HG00673.hp2 HG01109.hp1 HG02027.hp2 others(39): Show |
intron_variant | MODIFIER | c.1108-1192_1108-118 others(10): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
C | CGTGTGTG others(1): Show |
6 | a0001c0001t0002g0021a0001c0001t0002g0193a0001c0001t0002g0227others(3): Show | 9 | HG01975.hp1 HG02273.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.1108-1194_1108-118 others(12): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
C | CGTGTGTG others(3): Show |
10 | a0001c0001t0008g0053a0001c0001t0008g0056a0001c0001t0024g0023others(7): Show | 13 | HG01433.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1108-1196_1108-118 others(14): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
CGT | C | 2 | a0001c0001t0052g0172a0001c0005t0012g0025 | 3 | HG03041.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1108-1188_1108-118 others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117884813
|
CGTGT | C | 6 | a0001c0001t0005g0169a0001c0001t0006g0153a0001c0001t0029g0113others(3): Show | 6 | HG01175.hp2 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1108-1190_1108-118 others(8): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | ||||||
chr1:117885401
|
G | A | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1107+1176C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117885401 | ||||||
chr1:117885575
|
T | C | 1 | a0001c0001t0004g0094 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1107+1002A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117885575 | ||||||
chr1:117885858
|
T | C | 2 | a0001c0001t0015g0042a0001c0001t0015g0043 | 4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1107+719A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117885858 | ||||||
chr1:117886211
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1107+366C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117886211 | ||||||
chr1:117886364
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1107+213C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117886364 | ||||||
chr1:117886522
|
C | G | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1107+55G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117886522 | ||||||
chr1:117886816
|
G | GACA | 131 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(128): Show | 201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.1031-166_1031-164d others(5): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117886816 | ||||||
chr1:117886861
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1031-208G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117886861 | ||||||
chr1:117886910
|
A | G | 1 | a0001c0001t0034g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1031-257T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117886910 | ||||||
chr1:117886911
|
A | C | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1031-258T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117886911 | ||||||
chr1:117886991
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0006g0153a0001c0001t0006g0154 | 3 | HG02145.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1031-338A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117886991 | ||||||
chr1:117887008
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1031-355G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887008 | ||||||
chr1:117887133
|
G | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1031-480C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887133 | ||||||
chr1:117887149
|
T | C | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-496A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887149 | ||||||
chr1:117887193
|
G | A | 1 | a0001c0005t0012g0025 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1030+505C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887193 | ||||||
chr1:117887287
|
C | A | 20 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(17): Show | 25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1030+411G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887287 | ||||||
chr1:117887517
|
T | C | 1 | a0001c0001t0002g0197 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1030+181A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887517 | ||||||
chr1:117887852
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-78G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117887852 | ||||||
chr1:117888373
|
C | T | 1 | a0001c0001t0002g0044 | 2 | HG02056.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.954-599G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888373 | ||||||
chr1:117888704
|
T | TAAC | 1 | a0001c0001t0004g0005 | 5 | NA18956.hp2 NA18990.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.954-933_954-931dup others(3): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888704 | ||||||
chr1:117888784
|
A | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-1010T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888784 | ||||||
chr1:117888902
|
T | A | 3 | a0001c0001t0015g0042a0001c0001t0015g0043a0001c0001t0047g0191 | 5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.954-1128A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888902 | ||||||
chr1:117888967
|
A | G | 20 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(17): Show | 25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.954-1193T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888967 | ||||||
chr1:117888980
|
T | C | 20 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(17): Show | 25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.954-1206A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888980 | ||||||
chr1:117889079
|
A | G | 1 | a0001c0001t0051g0108 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.954-1305T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889079 | ||||||
chr1:117889146
|
C | T | 1 | a0001c0001t0005g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.954-1372G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889146 | ||||||
chr1:117889252
|
G | A | 1 | a0001c0003t0026g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.954-1478C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889252 | ||||||
chr1:117889314
|
AT | A | 42 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(39): Show | 70 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.954-1541delA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889314 | ||||||
chr1:117889718
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.954-1944C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889718 | ||||||
chr1:117889772
|
A | G | 4 | a0001c0001t0003g0027a0001c0001t0003g0083a0001c0001t0003g0084others(1): Show | 5 | HG00280.hp2 HG01243.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.954-1998T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889772 | ||||||
chr1:117889824
|
G | A | 6 | a0001c0002t0002g0020a0001c0002t0002g0186a0001c0002t0002g0187others(3): Show | 8 | HG01433.hp1 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.954-2050C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889824 | ||||||
chr1:117889853
|
T | C | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.954-2079A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889853 | ||||||
chr1:117889883
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-2109G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889883 | ||||||
chr1:117889885
|
A | G | 1 | a0001c0001t0038g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.954-2111T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889885 | ||||||
chr1:117890008
|
G | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-2234C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890008 | ||||||
chr1:117890065
|
G | A | 1 | a0001c0001t0023g0077 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.954-2291C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890065 | ||||||
chr1:117890197
|
T | C | 1 | a0001c0001t0002g0208 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.954-2423A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890197 | ||||||
chr1:117890270
|
G | A | 4 | a0001c0002t0002g0020a0001c0002t0002g0186a0001c0002t0002g0189others(1): Show | 6 | HG01433.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.954-2496C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890270 | ||||||
chr1:117890316
|
G | C | 65 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(62): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.954-2542C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890316 | ||||||
chr1:117890381
|
A | G | 1 | a0001c0001t0002g0206 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.954-2607T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890381 | ||||||
chr1:117890784
|
A | G | 2 | a0001c0001t0021g0040a0001c0001t0022g0174 | 3 | HG01884.hp2 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.954-3010T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890784 | ||||||
chr1:117890834
|
T | C | 1 | a0001c0002t0002g0186 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.954-3060A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890834 | ||||||
chr1:117891043
|
C | T | 1 | a0001c0001t0005g0220 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.954-3269G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891043 | ||||||
chr1:117891044
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.954-3270C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891044 | ||||||
chr1:117891265
|
G | A | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.954-3491C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891265 | ||||||
chr1:117891513
|
G | T | 1 | a0001c0001t0005g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.954-3739C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891513 | ||||||
chr1:117891514
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.954-3740A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891514 | ||||||
chr1:117891664
|
C | A | 2 | a0002c0004t0011g0216a0002c0004t0011g0217 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.954-3890G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891664 | ||||||
chr1:117891726
|
T | C | 1 | a0001c0001t0005g0181 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.954-3952A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891726 | ||||||
chr1:117891735
|
A | C | 2 | a0002c0004t0011g0216a0002c0004t0011g0217 | 2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.954-3961T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891735 | ||||||
chr1:117891765
|
T | C | 1 | a0001c0001t0043g0144 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.954-3991A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891765 | ||||||
chr1:117891770
|
G | A | 2 | a0001c0001t0015g0042a0001c0001t0015g0043 | 4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.954-3996C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891770 | ||||||
chr1:117891784
|
T | TA | 61 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(58): Show | 97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.954-4011dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891784 | ||||||
chr1:117891809
|
G | A | 2 | a0001c0001t0016g0008a0001c0001t0051g0108 | 5 | HG01361.hp1 HG01884.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.954-4035C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891809 | ||||||
chr1:117891850
|
A | G | 1 | a0001c0001t0047g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.954-4076T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891850 | ||||||
chr1:117891855
|
T | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.954-4081A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891855 | ||||||
chr1:117891942
|
T | G | 10 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(7): Show | 12 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.954-4168A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891942 | ||||||
chr1:117892066
|
G | C | 3 | a0001c0001t0003g0064a0001c0001t0003g0088a0001c0001t0034g0065 | 3 | HG02735.hp1 HG04199.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.954-4292C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892066 | ||||||
chr1:117892193
|
T | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-4419A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892193 | ||||||
chr1:117892337
|
T | C | 2 | a0001c0001t0001g0013a0001c0001t0001g0145 | 5 | HG01243.hp1 HG01257.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.953+4496A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892337 | ||||||
chr1:117892549
|
C | CTATTATT others(7): Show |
2 | a0001c0001t0015g0042a0001c0001t0015g0043 | 4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.953+4283_953+4284i others(16): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892549 | ||||||
chr1:117892653
|
A | G | 3 | a0001c0001t0001g0212a0001c0001t0002g0211a0001c0001t0002g0213 | 3 | NA18612.hp2 NA19064.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.953+4180T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892653 | ||||||
chr1:117892794
|
G | A | 133 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(130): Show | 203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.953+4039C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892794 | ||||||
chr1:117893107
|
T | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.953+3726A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117893107 | ||||||
chr1:117893230
|
G | A | 4 | a0001c0001t0003g0064a0001c0001t0003g0088a0001c0001t0034g0065others(1): Show | 4 | HG02135.hp2 HG02735.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.953+3603C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117893230 | ||||||
chr1:117893442
|
G | C | 1 | a0001c0001t0010g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.953+3391C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117893442 | ||||||
chr1:117893958
|
A | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.953+2875T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117893958 | ||||||
chr1:117894101
|
T | A | 1 | a0001c0001t0003g0028 | 2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.953+2732A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894101 | ||||||
chr1:117894179
|
G | A | 2 | a0001c0001t0003g0029a0001c0001t0004g0087 | 3 | HG01496.hp2 HG01928.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.953+2654C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894179 | ||||||
chr1:117894238
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.953+2595C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894238 | ||||||
chr1:117894256
|
T | C | 4 | a0001c0001t0003g0064a0001c0001t0003g0088a0001c0001t0034g0065others(1): Show | 4 | HG02135.hp2 HG02735.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.953+2577A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894256 | ||||||
chr1:117894281
|
C | T | 2 | a0001c0001t0015g0042a0001c0001t0015g0043 | 4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.953+2552G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894281 | ||||||
chr1:117894694
|
A | C | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.953+2139T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894694 | ||||||
chr1:117894770
|
T | C | 3 | a0001c0001t0015g0042a0001c0001t0015g0043a0001c0001t0047g0191 | 5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.953+2063A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894770 | ||||||
chr1:117894865
|
T | C | 1 | a0001c0001t0041g0146 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.953+1968A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894865 | ||||||
chr1:117894908
|
C | T | 3 | a0001c0001t0015g0042a0001c0001t0015g0043a0001c0001t0047g0191 | 5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.953+1925G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894908 | ||||||
chr1:117895039
|
C | T | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.953+1794G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117895039 | ||||||
chr1:117895207
|
A | G | 4 | a0001c0002t0002g0020a0001c0002t0002g0186a0001c0002t0002g0189others(1): Show | 6 | HG01433.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.953+1626T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117895207 | ||||||
chr1:117895371
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.953+1462G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117895371 | ||||||
chr1:117895592
|
G | A | 1 | a0001c0003t0017g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.953+1241C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117895592 | ||||||
chr1:117895806
|
G | A | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.953+1027C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117895806 | ||||||
chr1:117896662
|
T | C | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.953+171A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117896662 | ||||||
chr1:117896781
|
T | C | 1 | a0001c0001t0004g0079 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.953+52A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117896781 | ||||||
chr1:117897236
|
C | G | 4 | a0001c0001t0003g0027a0001c0001t0003g0083a0001c0001t0003g0084others(1): Show | 5 | HG00280.hp2 HG01243.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.797-247G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897236 | ||||||
chr1:117897373
|
T | C | 26 | a0001c0001t0003g0090a0001c0001t0004g0003a0001c0001t0004g0005others(23): Show | 46 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.797-384A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897373 | ||||||
chr1:117897548
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.797-559T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897548 | ||||||
chr1:117897706
|
C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0117a0001c0001t0001g0125others(3): Show | 10 | HG00558.hp2 NA18944.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.797-717G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897706 | ||||||
chr1:117897718
|
C | T | 1 | a0001c0001t0047g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.797-729G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897718 | ||||||
chr1:117897795
|
C | T | 1 | a0001c0001t0037g0130 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.797-806G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897795 | ||||||
chr1:117897808
|
G | A | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.797-819C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897808 | ||||||
chr1:117897942
|
T | C | 65 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(62): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.797-953A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897942 | ||||||
chr1:117898414
|
C | T | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.796+643G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898414 | ||||||
chr1:117898529
|
G | A | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+528C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898529 | ||||||
chr1:117898714
|
T | A | 1 | a0001c0001t0006g0154 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.796+343A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898714 | ||||||
chr1:117898757
|
C | T | 2 | a0001c0001t0002g0041a0001c0001t0002g0178 | 3 | HG02451.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.796+300G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898757 | ||||||
chr1:117898906
|
A | G | 1 | a0001c0001t0014g0129 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.796+151T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898906 | ||||||
chr1:117898998
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.796+59A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898998 | ||||||
chr1:117899012
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.796+45A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117899012 | ||||||
chr1:117899354
|
G | A | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.637-138C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117899354 | ||||||
chr1:117899551
|
A | C | 1 | a0001c0001t0005g0224 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.637-335T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117899551 | ||||||
chr1:117899675
|
A | C | 1 | a0001c0001t0004g0082 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.637-459T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117899675 | ||||||
chr1:117899766
|
A | G | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-550T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117899766 | ||||||
chr1:117899914
|
C | G | 136 | a0001c0001t0001g0062a0001c0001t0001g0195a0001c0001t0001g0212others(133): Show | 207 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.637-698G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117899914 | ||||||
chr1:117900078
|
T | TA | 3 | a0001c0001t0005g0219a0001c0001t0015g0042a0001c0001t0015g0043 | 5 | HG00140.hp2 HG00621.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-863dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900078 | ||||||
chr1:117900153
|
G | A | 3 | a0001c0001t0005g0115a0001c0001t0005g0181a0001c0001t0057g0180 | 3 | HG02257.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.637-937C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900153 | ||||||
chr1:117900394
|
C | T | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.637-1178G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900394 | ||||||
chr1:117900486
|
G | A | 1 | a0001c0002t0002g0188 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.637-1270C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900486 | ||||||
chr1:117900492
|
G | T | 1 | a0001c0001t0014g0129 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.637-1276C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900492 | ||||||
chr1:117900594
|
C | T | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-1378G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900594 | ||||||
chr1:117900631
|
T | G | 2 | a0001c0001t0015g0042a0001c0001t0015g0043 | 4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-1415A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900631 | ||||||
chr1:117900637
|
G | A | 1 | a0001c0001t0036g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637-1421C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900637 | ||||||
chr1:117900690
|
C | T | 1 | a0001c0003t0017g0230 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.637-1474G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900690 | ||||||
chr1:117900763
|
C | CA | 8 | a0001c0001t0001g0148a0001c0001t0002g0199a0001c0001t0002g0200others(5): Show | 8 | HG02602.hp2 HG03688.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.637-1548dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900763 | ||||||
chr1:117900763
|
CA | C | 10 | a0001c0001t0001g0126a0001c0001t0008g0024a0001c0001t0008g0053others(7): Show | 12 | HG01069.hp1 HG01975.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-1548delT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900763 | ||||||
chr1:117900783
|
G | A | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-1567C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900783 | ||||||
chr1:117900827
|
G | A | 1 | a0001c0001t0004g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.637-1611C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900827 | ||||||
chr1:117901024
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.637-1808A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901024 | ||||||
chr1:117901194
|
C | T | 1 | a0001c0001t0038g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.637-1978G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901194 | ||||||
chr1:117901223
|
C | T | 1 | a0001c0001t0018g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.637-2007G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901223 | ||||||
chr1:117901346
|
T | G | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-2130A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901346 | ||||||
chr1:117901352
|
T | C | 2 | a0001c0001t0019g0039a0001c0001t0019g0167 | 3 | NA18944.hp2 NA18984.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.637-2136A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901352 | ||||||
chr1:117901566
|
G | C | 1 | a0001c0001t0001g0151 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.637-2350C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901566 | ||||||
chr1:117901631
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.637-2415G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901631 | ||||||
chr1:117901690
|
A | AT | 23 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(20): Show | 30 | HG00621.hp1 HG01175.hp2 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.637-2475dupA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901690 | ||||||
chr1:117901830
|
A | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-2614T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901830 | ||||||
chr1:117901864
|
C | A | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-2648G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901864 | ||||||
chr1:117902257
|
A | G | 2 | a0001c0001t0002g0194a0001c0001t0002g0204 | 2 | NA18974.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.637-3041T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902257 | ||||||
chr1:117902457
|
T | C | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.637-3241A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902457 | ||||||
chr1:117902512
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.637-3296A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902512 | ||||||
chr1:117902548
|
G | A | 3 | a0001c0001t0003g0014a0001c0001t0003g0067a0001c0001t0032g0066 | 5 | HG01167.hp1 HG01358.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-3332C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902548 | ||||||
chr1:117902622
|
C | A | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-3406G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902622 | ||||||
chr1:117902798
|
A | T | 1 | a0001c0001t0001g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.637-3582T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902798 | ||||||
chr1:117902844
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0126 | 4 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-3628C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902844 | ||||||
chr1:117902974
|
A | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.636+3532T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902974 | ||||||
chr1:117903043
|
T | C | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.636+3463A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903043 | ||||||
chr1:117903105
|
T | C | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.636+3401A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903105 | ||||||
chr1:117903165
|
G | T | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+3341C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903165 | ||||||
chr1:117903169
|
T | C | 1 | a0001c0001t0005g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.636+3337A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903169 | ||||||
chr1:117903212
|
G | A | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+3294C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903212 | ||||||
chr1:117903329
|
G | A | 1 | a0001c0001t0005g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.636+3177C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903329 | ||||||
chr1:117903543
|
T | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.636+2963A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903543 | ||||||
chr1:117903707
|
G | C | 1 | a0001c0001t0007g0160 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.636+2799C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903707 | ||||||
chr1:117903749
|
G | A | 8 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(5): Show | 9 | HG01975.hp1 HG02273.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.636+2757C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903749 | ||||||
chr1:117903786
|
C | T | 1 | a0001c0005t0012g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.636+2720G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903786 | ||||||
chr1:117903815
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0045g0127 | 3 | NA18950.hp2 NA18986.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.636+2691T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903815 | ||||||
chr1:117903891
|
T | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+2615A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903891 | ||||||
chr1:117904314
|
T | C | 16 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(13): Show | 19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.636+2192A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117904314 | ||||||
chr1:117904397
|
T | A | 1 | a0001c0001t0004g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.636+2109A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117904397 | ||||||
chr1:117904644
|
T | C | 4 | a0001c0001t0001g0062a0001c0001t0018g0026a0001c0001t0018g0061others(1): Show | 5 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.636+1862A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117904644 | ||||||
chr1:117904846
|
G | A | 1 | a0001c0001t0003g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.636+1660C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117904846 | ||||||
chr1:117905044
|
A | C | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+1462T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905044 | ||||||
chr1:117905062
|
T | C | 1 | a0001c0001t0004g0096 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.636+1444A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905062 | ||||||
chr1:117905264
|
A | T | 1 | a0001c0001t0003g0103 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.636+1242T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905264 | ||||||
chr1:117905317
|
T | C | 1 | a0001c0001t0003g0097 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.636+1189A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905317 | ||||||
chr1:117905423
|
C | T | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+1083G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905423 | ||||||
chr1:117905458
|
T | C | 2 | a0001c0001t0020g0098a0001c0001t0020g0110 | 2 | HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.636+1048A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905458 | ||||||
chr1:117905862
|
C | T | 1 | a0001c0001t0047g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.636+644G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905862 | ||||||
chr1:117906022
|
A | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.636+484T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117906022 | ||||||
chr1:117906068
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0006g0153a0001c0001t0006g0154 | 3 | HG02145.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.636+438A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117906068 | ||||||
chr1:117906147
|
G | T | 2 | a0001c0001t0021g0040a0001c0001t0022g0174 | 3 | HG01884.hp2 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.636+359C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117906147 | ||||||
chr1:117906345
|
A | G | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+161T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117906345 | ||||||
chr1:117906486
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.636+20G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117906486 | ||||||
chr1:117906593
|
G | A | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.560-11C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117906593 | ||||||
chr1:117906635
|
A | G | 1 | a0001c0001t0038g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.560-53T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117906635 | ||||||
chr1:117906855
|
A | C | 2 | a0001c0001t0015g0042a0001c0001t0015g0043 | 4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-273T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117906855 | ||||||
chr1:117906903
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.560-321C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117906903 | ||||||
chr1:117906993
|
G | A | 1 | a0001c0001t0008g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.560-411C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117906993 | ||||||
chr1:117907065
|
C | A | 1 | a0001c0001t0010g0099 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.560-483G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907065 | ||||||
chr1:117907255
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.560-673G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907255 | ||||||
chr1:117907378
|
T | G | 1 | a0001c0001t0039g0155 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.560-796A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907378 | ||||||
chr1:117907421
|
G | C | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.560-839C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907421 | ||||||
chr1:117907504
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.560-922G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907504 | ||||||
chr1:117907629
|
T | C | 8 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(5): Show | 9 | HG01975.hp1 HG02273.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.560-1047A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907629 | ||||||
chr1:117907771
|
G | A | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.560-1189C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907771 | ||||||
chr1:117907818
|
C | T | 1 | a0001c0001t0038g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.560-1236G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907818 | ||||||
chr1:117907819
|
G | A | 1 | a0001c0001t0003g0100 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560-1237C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907819 | ||||||
chr1:117907944
|
C | T | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.560-1362G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907944 | ||||||
chr1:117907959
|
C | G | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.560-1377G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907959 | ||||||
chr1:117908131
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.560-1549G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908131 | ||||||
chr1:117908299
|
G | A | 4 | a0001c0001t0029g0113a0002c0004t0011g0022a0002c0004t0011g0216others(1): Show | 6 | HG01175.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-1717C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908299 | ||||||
chr1:117908548
|
C | T | 16 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(13): Show | 19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.560-1966G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908548 | ||||||
chr1:117908598
|
C | T | 1 | a0001c0003t0027g0048 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.560-2016G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908598 | ||||||
chr1:117908669
|
T | A | 9 | a0001c0001t0005g0171a0001c0001t0005g0224a0001c0003t0017g0229others(6): Show | 10 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.560-2087A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908669 | ||||||
chr1:117908670
|
A | T | 1 | a0001c0001t0054g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.560-2088T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908670 | ||||||
chr1:117908720
|
G | A | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.560-2138C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908720 | ||||||
chr1:117908728
|
C | A | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.560-2146G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908728 | ||||||
chr1:117908811
|
T | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.560-2229A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908811 | ||||||
chr1:117908828
|
A | AAAAT | 37 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(34): Show | 63 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.560-2250_560-2247d others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908828 | ||||||
chr1:117908828
|
AAAAT | A | 15 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(12): Show | 21 | HG00621.hp1 HG01975.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.560-2250_560-2247d others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908828 | ||||||
chr1:117908832
|
T | A | 1 | a0001c0001t0005g0220 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.560-2250A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908832 | ||||||
chr1:117908836
|
T | A | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.560-2254A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908836 | ||||||
chr1:117908840
|
T | A | 2 | a0001c0001t0029g0113a0002c0004t0011g0217 | 2 | HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.560-2258A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908840 | ||||||
chr1:117908844
|
T | A | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.560-2262A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908844 | ||||||
chr1:117909432
|
T | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+2562A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909432 | ||||||
chr1:117909540
|
A | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.559+2454T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909540 | ||||||
chr1:117909612
|
A | T | 20 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(17): Show | 25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.559+2382T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909612 | ||||||
chr1:117909732
|
A | G | 1 | a0001c0001t0038g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.559+2262T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909732 | ||||||
chr1:117909765
|
T | C | 31 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(28): Show | 55 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.559+2229A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909765 | ||||||
chr1:117909795
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+2199G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909795 | ||||||
chr1:117909895
|
C | T | 1 | a0001c0001t0002g0210 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.559+2099G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909895 | ||||||
chr1:117909965
|
T | C | 65 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(62): Show | 101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.559+2029A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909965 | ||||||
chr1:117910036
|
T | C | 3 | a0001c0001t0015g0042a0001c0001t0015g0043a0001c0001t0047g0191 | 5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.559+1958A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910036 | ||||||
chr1:117910106
|
T | C | 1 | a0001c0001t0005g0170 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.559+1888A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910106 | ||||||
chr1:117910115
|
A | G | 1 | a0001c0001t0005g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.559+1879T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910115 | ||||||
chr1:117910208
|
A | G | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.559+1786T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910208 | ||||||
chr1:117910227
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0126 | 4 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+1767G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910227 | ||||||
chr1:117910271
|
GGA | G | 41 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(38): Show | 68 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.559+1721_559+1722d others(4): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910271 | ||||||
chr1:117910281
|
C | G | 3 | a0001c0001t0004g0070a0001c0001t0004g0081a0001c0001t0010g0080 | 3 | NA18985.hp1 NA19057.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.559+1713G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910281 | ||||||
chr1:117910282
|
T | C | 1 | a0001c0001t0036g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.559+1712A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910282 | ||||||
chr1:117910336
|
A | T | 2 | a0001c0001t0015g0042a0001c0001t0015g0043 | 4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+1658T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910336 | ||||||
chr1:117910509
|
A | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.559+1485T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910509 | ||||||
chr1:117910677
|
C | T | 1 | a0001c0001t0038g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.559+1317G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910677 | ||||||
chr1:117910775
|
T | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+1219A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910775 | ||||||
chr1:117910911
|
T | C | 2 | a0001c0001t0007g0157a0001c0001t0007g0159 | 2 | NA18985.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.559+1083A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910911 | ||||||
chr1:117911007
|
C | A | 4 | a0001c0001t0002g0192a0001c0001t0002g0203a0001c0001t0002g0227others(1): Show | 4 | HG00673.hp2 HG02071.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+987G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911007 | ||||||
chr1:117911037
|
G | A | 31 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(28): Show | 55 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.559+957C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911037 | ||||||
chr1:117911515
|
G | A | 1 | a0001c0001t0003g0076 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.559+479C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911515 | ||||||
chr1:117911642
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+352G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911642 | ||||||
chr1:117911754
|
T | TA | 9 | a0001c0001t0002g0045a0001c0001t0002g0204a0001c0001t0007g0118others(6): Show | 11 | HG01433.hp1 HG02074.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+239dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911754 | ||||||
chr1:117911766
|
A | C | 2 | a0001c0001t0003g0071a0001c0001t0003g0102 | 2 | HG02056.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.559+228T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911766 | ||||||
chr1:117911780
|
T | G | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.559+214A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911780 | ||||||
chr1:117912273
|
G | C | 1 | a0001c0001t0003g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.471-191C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 4/13 | chr1 | 117912273 | ||||||
chr1:117912718
|
T | C | 1 | a0001c0001t0004g0101 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.317-35A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117912718 | ||||||
chr1:117913018
|
C | T | 1 | a0001c0001t0003g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-335G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913018 | ||||||
chr1:117913019
|
G | A | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-336C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913019 | ||||||
chr1:117913024
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.317-341T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913024 | ||||||
chr1:117913035
|
T | C | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.317-352A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913035 | ||||||
chr1:117913132
|
C | T | 132 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(129): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.317-449G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913132 | ||||||
chr1:117913172
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.317-489G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913172 | ||||||
chr1:117913401
|
A | AT | 9 | a0001c0001t0002g0193a0001c0001t0003g0075a0001c0001t0004g0079others(6): Show | 10 | HG01175.hp2 HG02135.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-719dupA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913401 | ||||||
chr1:117914080
|
C | T | 1 | a0001c0001t0046g0124 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.317-1397G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914080 | ||||||
chr1:117914107
|
T | C | 1 | a0001c0001t0003g0107 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.317-1424A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914107 | ||||||
chr1:117914176
|
A | G | 6 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(3): Show | 7 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.317-1493T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914176 | ||||||
chr1:117914291
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0005g0123 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.317-1608G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914291 | ||||||
chr1:117914448
|
C | T | 2 | a0001c0001t0015g0042a0001c0001t0015g0043 | 4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-1765G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914448 | ||||||
chr1:117914794
|
C | T | 1 | a0001c0001t0005g0173 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.317-2111G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914794 | ||||||
chr1:117914975
|
G | T | 1 | a0001c0001t0052g0172 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.317-2292C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914975 | ||||||
chr1:117915018
|
G | T | 1 | a0001c0001t0003g0073 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-2335C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915018 | ||||||
chr1:117915382
|
C | A | 1 | a0001c0003t0026g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.317-2699G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915382 | ||||||
chr1:117915519
|
G | A | 1 | a0001c0001t0036g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.317-2836C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915519 | ||||||
chr1:117915648
|
T | C | 1 | a0001c0001t0007g0160 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.316+2949A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915648 | ||||||
chr1:117915800
|
AT | A | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+2796delA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915800 | ||||||
chr1:117915815
|
C | T | 1 | a0001c0001t0036g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+2782G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915815 | ||||||
chr1:117915832
|
TTGACATA others(8): Show |
T | 1 | a0001c0001t0003g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.316+2750_316+2764d others(17): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915832 | ||||||
chr1:117915840
|
T | C | 41 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(38): Show | 68 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.316+2757A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915840 | ||||||
chr1:117915925
|
T | C | 2 | a0001c0001t0018g0026a0001c0001t0048g0063 | 3 | HG02723.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.316+2672A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915925 | ||||||
chr1:117916119
|
T | G | 4 | a0001c0001t0005g0047a0001c0001t0005g0219a0001c0001t0005g0220others(1): Show | 5 | HG00140.hp2 HG01361.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+2478A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916119 | ||||||
chr1:117916123
|
G | A | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+2474C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916123 | ||||||
chr1:117916165
|
G | C | 2 | a0001c0001t0015g0042a0001c0001t0015g0043 | 4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+2432C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916165 | ||||||
chr1:117916316
|
C | T | 2 | a0001c0001t0005g0171a0001c0001t0005g0224 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.316+2281G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916316 | ||||||
chr1:117916327
|
G | C | 1 | a0001c0003t0026g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.316+2270C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916327 | ||||||
chr1:117916359
|
A | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+2238T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916359 | ||||||
chr1:117916419
|
G | A | 1 | a0001c0001t0038g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.316+2178C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916419 | ||||||
chr1:117916695
|
G | T | 1 | a0001c0001t0036g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+1902C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916695 | ||||||
chr1:117916906
|
C | T | 1 | a0001c0001t0021g0040 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.316+1691G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916906 | ||||||
chr1:117917297
|
G | A | 1 | a0001c0001t0002g0205 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.316+1300C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917297 | ||||||
chr1:117917369
|
C | A | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+1228G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917369 | ||||||
chr1:117917527
|
A | G | 4 | a0001c0001t0005g0018a0001c0001t0005g0169a0001c0001t0005g0170others(1): Show | 6 | HG02630.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.316+1070T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917527 | ||||||
chr1:117917528
|
T | C | 1 | a0001c0001t0002g0213 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.316+1069A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917528 | ||||||
chr1:117917604
|
G | A | 1 | a0001c0001t0034g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.316+993C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917604 | ||||||
chr1:117917723
|
T | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+874A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917723 | ||||||
chr1:117917788
|
T | C | 1 | a0001c0001t0005g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.316+809A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917788 | ||||||
chr1:117917789
|
A | G | 1 | a0001c0001t0018g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.316+808T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917789 | ||||||
chr1:117917897
|
C | T | 1 | a0001c0001t0036g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+700G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917897 | ||||||
chr1:117917982
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0119a0001c0001t0009g0120others(1): Show | 7 | HG01952.hp1 HG02083.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.316+615T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917982 | ||||||
chr1:117918075
|
T | C | 1 | a0001c0001t0014g0161 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.316+522A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117918075 | ||||||
chr1:117918897
|
C | CAATT | 20 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(17): Show | 25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.177-162_177-161ins others(4): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117918897 | ||||||
chr1:117919096
|
C | T | 11 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0071others(8): Show | 13 | HG00642.hp2 HG01069.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.177-360G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919096 | ||||||
chr1:117919102
|
C | T | 10 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0071others(7): Show | 12 | HG00642.hp2 HG01069.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.177-366G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919102 | ||||||
chr1:117919112
|
T | C | 10 | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0071others(7): Show | 12 | HG00642.hp2 HG01069.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.177-376A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919112 | ||||||
chr1:117919370
|
C | CA | 14 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(11): Show | 17 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.177-635dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919370 | ||||||
chr1:117919370
|
C | CAAA | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.177-637_177-635dup others(3): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919370 | ||||||
chr1:117919530
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.176+652G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919530 | ||||||
chr1:117919539
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.176+643G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919539 | ||||||
chr1:117919742
|
T | C | 1 | a0001c0001t0003g0034 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.176+440A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919742 | ||||||
chr1:117919772
|
C | T | 4 | a0001c0001t0001g0062a0001c0001t0018g0026a0001c0001t0018g0061others(1): Show | 5 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.176+410G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919772 | ||||||
chr1:117919874
|
T | C | 1 | a0001c0001t0006g0162 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.176+308A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919874 | ||||||
chr1:117920063
|
A | G | 3 | a0001c0001t0003g0006a0001c0001t0003g0075a0001c0001t0003g0076 | 6 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.176+119T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117920063 | ||||||
chr1:117920646
|
G | T | 66 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(63): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-67-222C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920646 | ||||||
chr1:117920673
|
GCCCACCA others(17): Show |
G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67-273_-67-250del others(24): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920673 | ||||||
chr1:117920715
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-67-291G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920715 | ||||||
chr1:117920737
|
G | GA | 6 | a0001c0001t0007g0163a0001c0001t0015g0042a0001c0001t0015g0043others(3): Show | 10 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.-67-314dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920737 | ||||||
chr1:117920737
|
GA | G | 53 | a0001c0001t0001g0119a0001c0001t0001g0195a0001c0001t0001g0212others(50): Show | 82 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.-67-314delT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920737 | ||||||
chr1:117920947
|
A | G | 1 | a0001c0001t0007g0118 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-67-523T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920947 | ||||||
chr1:117920983
|
T | C | 1 | a0001c0001t0001g0164 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-67-559A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920983 | ||||||
chr1:117921003
|
T | C | 1 | a0001c0001t0004g0109 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-67-579A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117921003 | ||||||
chr1:117921239
|
T | TA | 64 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(61): Show | 100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.-67-816dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117921239 | ||||||
chr1:117921344
|
T | C | 20 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(17): Show | 25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.-67-920A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117921344 | ||||||
chr1:117921922
|
G | C | 2 | a0001c0001t0001g0166a0001c0001t0009g0165 | 2 | NA18948.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-67-1498C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117921922 | ||||||
chr1:117922043
|
G | GT | 10 | a0001c0001t0004g0072a0001c0001t0008g0024a0001c0001t0008g0053others(7): Show | 12 | HG00597.hp1 HG01975.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-67-1620dupA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922043 | ||||||
chr1:117922043
|
GT | G | 7 | a0001c0001t0001g0183a0001c0001t0005g0019a0001c0001t0005g0047others(4): Show | 10 | HG00140.hp2 HG01361.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.-67-1620delA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922043 | ||||||
chr1:117922175
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-67-1751A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922175 | ||||||
chr1:117922227
|
T | C | 7 | a0001c0003t0017g0229a0001c0003t0017g0230a0001c0003t0017g0232others(4): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-67-1803A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922227 | ||||||
chr1:117922238
|
G | T | 1 | a0001c0001t0003g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-67-1814C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922238 | ||||||
chr1:117922285
|
A | G | 3 | a0001c0001t0015g0042a0001c0001t0015g0043a0001c0001t0047g0191 | 5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-1861T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922285 | ||||||
chr1:117922429
|
T | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67-2005A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922429 | ||||||
chr1:117922446
|
A | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67-2022T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922446 | ||||||
chr1:117922478
|
C | T | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-2054G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922478 | ||||||
chr1:117922594
|
G | C | 1 | a0001c0001t0019g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-67-2170C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922594 | ||||||
chr1:117922799
|
C | T | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-67-2375G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922799 | ||||||
chr1:117922803
|
T | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67-2379A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922803 | ||||||
chr1:117922829
|
G | A | 1 | a0001c0001t0020g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-67-2405C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922829 | ||||||
chr1:117922941
|
C | T | 6 | a0001c0002t0002g0020a0001c0002t0002g0186a0001c0002t0002g0187others(3): Show | 8 | HG01433.hp1 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-67-2517G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922941 | ||||||
chr1:117923050
|
C | T | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-2626G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923050 | ||||||
chr1:117923137
|
C | T | 1 | a0001c0001t0004g0070 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-67-2713G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923137 | ||||||
chr1:117923209
|
T | C | 7 | a0001c0001t0001g0183a0001c0001t0005g0019a0001c0001t0005g0047others(4): Show | 10 | HG00140.hp2 HG01361.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.-67-2785A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923209 | ||||||
chr1:117923234
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-67-2810C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923234 | ||||||
chr1:117923814
|
C | G | 1 | a0001c0001t0003g0069 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-67-3390G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923814 | ||||||
chr1:117923927
|
C | T | 2 | a0001c0001t0025g0050a0001c0001t0025g0051 | 2 | HG02698.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-67-3503G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923927 | ||||||
chr1:117923962
|
T | C | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-67-3538A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923962 | ||||||
chr1:117924188
|
T | C | 1 | a0001c0001t0005g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-67-3764A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924188 | ||||||
chr1:117924514
|
A | C | 1 | a0001c0001t0030g0185 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-67-4090T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924514 | ||||||
chr1:117924515
|
C | A | 1 | a0001c0001t0030g0185 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-67-4091G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924515 | ||||||
chr1:117924633
|
C | T | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-4209G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924633 | ||||||
chr1:117924706
|
T | C | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-4282A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924706 | ||||||
chr1:117924912
|
T | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-4488A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924912 | ||||||
chr1:117925016
|
G | A | 165 | a0001c0001t0001g0062a0001c0001t0001g0116a0001c0001t0001g0183others(162): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-68+4432C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925016 | ||||||
chr1:117925140
|
T | G | 1 | a0001c0001t0008g0055 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-68+4308A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925140 | ||||||
chr1:117925148
|
G | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+4300C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925148 | ||||||
chr1:117925181
|
A | G | 65 | a0001c0001t0001g0195a0001c0001t0001g0212a0001c0001t0002g0002others(62): Show | 99 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.-68+4267T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925181 | ||||||
chr1:117925191
|
A | G | 3 | a0001c0001t0003g0014a0001c0001t0003g0067a0001c0001t0032g0066 | 5 | HG01167.hp1 HG01358.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+4257T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925191 | ||||||
chr1:117925510
|
T | A | 1 | a0001c0001t0030g0185 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-68+3938A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925510 | ||||||
chr1:117925512
|
C | T | 1 | a0001c0001t0030g0185 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-68+3936G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925512 | ||||||
chr1:117925576
|
G | A | 1 | a0001c0001t0002g0210 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-68+3872C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925576 | ||||||
chr1:117925652
|
G | A | 20 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(17): Show | 25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.-68+3796C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925652 | ||||||
chr1:117925801
|
A | T | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+3647T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925801 | ||||||
chr1:117925888
|
C | T | 13 | a0001c0001t0001g0062a0001c0001t0008g0024a0001c0001t0008g0053others(10): Show | 16 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(13): Show |
intron_variant | MODIFIER | c.-68+3560G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925888 | ||||||
chr1:117925894
|
GAGGGTAT others(5): Show |
G | 1 | a0001c0001t0001g0117 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-68+3542_-68+3553d others(14): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925894 | ||||||
chr1:117925914
|
T | C | 1 | a0001c0001t0008g0056 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-68+3534A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925914 | ||||||
chr1:117925922
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-68+3526G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925922 | ||||||
chr1:117925997
|
T | C | 3 | a0001c0001t0001g0212a0001c0001t0002g0211a0001c0001t0002g0213 | 3 | NA18612.hp2 NA19064.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-68+3451A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925997 | ||||||
chr1:117926126
|
T | C | 1 | a0001c0001t0036g0214 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-68+3322A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926126 | ||||||
chr1:117926174
|
C | T | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+3274G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926174 | ||||||
chr1:117926220
|
A | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+3228T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926220 | ||||||
chr1:117926329
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-68+3119A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926329 | ||||||
chr1:117926614
|
C | G | 1 | a0001c0001t0005g0115 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-68+2834G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926614 | ||||||
chr1:117926661
|
A | G | 1 | a0001c0001t0030g0185 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-68+2787T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926661 | ||||||
chr1:117926671
|
T | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+2777A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926671 | ||||||
chr1:117927002
|
T | TA | 122 | a0001c0001t0001g0062a0001c0001t0001g0195a0001c0001t0001g0212others(119): Show | 190 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.-68+2445dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927002 | ||||||
chr1:117927002
|
T | TAA | 11 | a0001c0001t0002g0046a0001c0001t0002g0215a0001c0001t0008g0024others(8): Show | 14 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.-68+2444_-68+2445d others(4): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927002 | ||||||
chr1:117927139
|
C | G | 1 | a0001c0003t0017g0229 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-68+2309G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927139 | ||||||
chr1:117927219
|
G | GT | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+2228dupA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927219 | ||||||
chr1:117927293
|
G | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+2155C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927293 | ||||||
chr1:117927334
|
A | C | 1 | a0001c0005t0012g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-68+2114T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927334 | ||||||
chr1:117927379
|
T | C | 1 | a0001c0001t0004g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-68+2069A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927379 | ||||||
chr1:117927529
|
A | C | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+1919T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927529 | ||||||
chr1:117927568
|
A | G | 1 | a0001c0008t0001g0114 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-68+1880T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927568 | ||||||
chr1:117927662
|
T | G | 9 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(6): Show | 11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+1786A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927662 | ||||||
chr1:117927952
|
T | C | 3 | a0002c0004t0011g0022a0002c0004t0011g0216a0002c0004t0011g0217 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+1496A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927952 | ||||||
chr1:117928209
|
C | A | 4 | a0001c0001t0005g0047a0001c0001t0005g0219a0001c0001t0005g0220others(1): Show | 5 | HG00140.hp2 HG01361.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+1239G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928209 | ||||||
chr1:117928344
|
A | G | 1 | a0001c0001t0029g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-68+1104T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928344 | ||||||
chr1:117928415
|
T | C | 16 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(13): Show | 19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-68+1033A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928415 | ||||||
chr1:117928438
|
G | A | 2 | a0003c0006t0001g0222a0003c0006t0006g0221 | 2 | HG00438.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.-68+1010C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928438 | ||||||
chr1:117928589
|
C | T | 66 | a0001c0001t0003g0006a0001c0001t0003g0014a0001c0001t0003g0027others(63): Show | 102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-68+859G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928589 | ||||||
chr1:117928697
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-68+751A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928697 | ||||||
chr1:117928777
|
A | C | 4 | a0001c0001t0001g0062a0001c0001t0018g0026a0001c0001t0018g0061others(1): Show | 5 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+671T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928777 | ||||||
chr1:117928850
|
A | G | 3 | a0001c0005t0012g0025a0001c0005t0012g0059a0001c0005t0012g0060 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+598T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928850 | ||||||
chr1:117928916
|
G | A | 1 | a0001c0001t0005g0224 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-68+532C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928916 | ||||||
chr1:117928960
|
G | T | 1 | a0001c0001t0035g0058 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-68+488C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928960 | ||||||
chr1:117928967
|
G | A | 2 | a0001c0001t0005g0225a0001c0001t0053g0226 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-68+481C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928967 | ||||||
chr1:117929034
|
T | C | 1 | a0001c0001t0002g0227 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-68+414A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117929034 | ||||||
chr1:117929077
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-68+371A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117929077 | ||||||
chr1:117929130
|
A | C | 1 | a0001c0001t0038g0057 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-68+318T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117929130 | ||||||
chr1:117929323
|
A | C | 16 | a0001c0001t0008g0024a0001c0001t0008g0053a0001c0001t0008g0054others(13): Show | 19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-68+125T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117929323 |