Item | Value |
---|---|
geneid | 2820 |
ensemblid | ENSG00000115159.17 |
hgncid | 4456 |
symbol | GPD2 |
name | glycerol-3-phosphate dehydrogenase 2 |
refseq_nuc | NM_000408.5 |
refseq_prot | NP_000399.3 |
ensembl_nuc | ENST00000438166.7 |
ensembl_prot | ENSP00000409708.2 |
mane_status | MANE Select |
chr | chr2 |
start | 156436379 |
end | 156586403 |
strand | + |
ver | v1.2 |
region | chr2:156436379-156586403 |
region5000 | chr2:156431379-156591403 |
regionname0 | GPD2_chr2_156436379_156586403 |
regionname5000 | GPD2_chr2_156431379_156591403 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 727 | 167 | 27 | 25 | 86 | 4 | 25 | 65 | GPD2_chr2_156431379_156591403 | GPD2 | MAFQK others(722): Show |
chr2 | 156431379 | 156591403 |
a0002 | 1/1 | 727 | 78 | 23 | 17 | 27 | 2 | 7 | 20 | GPD2_chr2_156431379_156591403 | GPD2 | MAFQK others(722): Show |
chr2 | 156431379 | 156591403 |
a0003 | 0/0 | 727 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | MAFQK others(722): Show |
chr2 | 156431379 | 156591403 |
a0004 | 0/0 | 727 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | MAFQK others(722): Show |
chr2 | 156431379 | 156591403 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2181 | 160 | 27 | 24 | 82 | 3 | 24 | GPD2_chr2_156431379_156591403 | GPD2 | ATGGC others(2176): Show |
chr2 | 156431379 | 156591403 | ||
a0001c0004 | 0/0 | 2181 | 3 | 0 | 1 | 0 | 1 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | ATGGC others(2176): Show |
chr2 | 156431379 | 156591403 | ||
a0001c0005 | 0/0 | 2181 | 2 | 0 | 0 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | ATGGC others(2176): Show |
chr2 | 156431379 | 156591403 | ||
a0001c0006 | 0/0 | 2181 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | ATGGC others(2176): Show |
chr2 | 156431379 | 156591403 | ||
a0001c0007 | 0/0 | 2181 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | ATGGC others(2176): Show |
chr2 | 156431379 | 156591403 | ||
a0002c0002 | 1/1 | 2181 | 78 | 23 | 17 | 27 | 2 | 7 | GPD2_chr2_156431379_156591403 | GPD2 | ATGGC others(2176): Show |
chr2 | 156431379 | 156591403 | ||
a0003c0003 | 0/0 | 2181 | 8 | 8 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | ATGGC others(2176): Show |
chr2 | 156431379 | 156591403 | ||
a0004c0008 | 0/0 | 2181 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | ATGGC others(2176): Show |
chr2 | 156431379 | 156591403 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5812 | 125 | 18 | 21 | 65 | 3 | 18 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0001c0001t0003 | 0/0 | 5810 | 18 | 2 | 2 | 9 | 0 | 5 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5805): Show |
chr2 | 156431379 | 156591403 |
a0001c0001t0005 | 0/0 | 5812 | 7 | 7 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0001c0001t0010 | 0/0 | 5812 | 4 | 0 | 0 | 4 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0001c0001t0013 | 0/0 | 5812 | 2 | 0 | 0 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0001c0001t0015 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0001c0001t0016 | 0/0 | 5812 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0001c0001t0017 | 0/0 | 5812 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0001c0001t0018 | 0/0 | 5810 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5805): Show |
chr2 | 156431379 | 156591403 |
a0001c0004t0001 | 0/0 | 5812 | 3 | 0 | 1 | 0 | 1 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0001c0005t0001 | 0/0 | 5812 | 2 | 0 | 0 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0001c0006t0001 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0001c0007t0001 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0001 | 0/0 | 5812 | 5 | 4 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0002 | 0/1 | 5812 | 32 | 7 | 6 | 12 | 1 | 5 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0004 | 0/0 | 5812 | 11 | 0 | 0 | 11 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0005 | 0/0 | 5812 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0006 | 0/0 | 5812 | 8 | 3 | 3 | 2 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0008 | 1/0 | 5812 | 5 | 4 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0009 | 0/0 | 5812 | 5 | 0 | 5 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0011 | 0/0 | 5812 | 3 | 0 | 1 | 0 | 0 | 2 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0012 | 0/0 | 5812 | 3 | 3 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0014 | 0/0 | 5812 | 2 | 0 | 2 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0019 | 0/0 | 5812 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0020 | 0/0 | 5812 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0002c0002t0021 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0003c0003t0005 | 0/0 | 5812 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0003c0003t0007 | 0/0 | 5812 | 7 | 7 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
a0004c0008t0001 | 0/0 | 5812 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | GAGTG others(5807): Show |
chr2 | 156431379 | 156591403 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0010g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0010g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0010g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0013g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0013g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0015g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0016g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0017g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0001t0018g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0006t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0001c0007t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0008g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0009g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0009g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0009g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0009g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0011g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0011g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0011g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0014g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0014g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0019g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0020g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0002c0002t0021g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0003c0003t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0003c0003t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0003c0003t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0003c0003t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0003c0003t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0003c0003t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0003c0003t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0003c0003t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
a0004c0008t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00140 | hp2 | a0001 | c0004 | t0001 | g0219 | EUR | GBR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | FIN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0122 | EUR | FIN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00438 | hp1 | a0001 | c0001 | t0010 | g0128 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00438 | hp2 | a0002 | c0002 | t0004 | g0025 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00621 | hp1 | a0002 | c0002 | t0004 | g0028 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00673 | hp2 | a0002 | c0002 | t0006 | g0039 | EAS | CHS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00735 | hp1 | a0002 | c0002 | t0006 | g0156 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01070 | hp2 | a0002 | c0002 | t0014 | g0067 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01099 | hp2 | a0002 | c0002 | t0006 | g0155 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0085 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0125 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01192 | hp2 | a0002 | c0002 | t0014 | g0078 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01243 | hp1 | a0002 | c0002 | t0006 | g0157 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0147 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01261 | hp2 | a0001 | c0001 | t0016 | g0049 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01346 | hp2 | a0002 | c0002 | t0009 | g0120 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0152 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01433 | hp1 | a0001 | c0004 | t0001 | g0199 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01433 | hp2 | a0002 | c0002 | t0009 | g0118 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01496 | hp1 | a0002 | c0002 | t0009 | g0119 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01496 | hp2 | a0002 | c0002 | t0011 | g0051 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01517 | hp2 | a0002 | c0002 | t0020 | g0021 | EUR | IBS | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0150 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01891 | hp1 | a0003 | c0003 | t0007 | g0063 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01891 | hp2 | a0003 | c0003 | t0005 | g0158 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01928 | hp1 | a0002 | c0002 | t0009 | g0034 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01975 | hp1 | a0002 | c0002 | t0009 | g0137 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02055 | hp1 | a0003 | c0003 | t0007 | g0012 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0149 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02056 | hp1 | a0001 | c0001 | t0015 | g0098 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02071 | hp2 | a0001 | c0001 | t0010 | g0031 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02074 | hp2 | a0002 | c0002 | t0021 | g0054 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CDX | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02258 | hp1 | a0002 | c0002 | t0006 | g0154 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02258 | hp2 | a0002 | c0002 | t0012 | g0075 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0151 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02523 | hp2 | a0001 | c0001 | t0013 | g0069 | EAS | KHV | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0030 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0180 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02630 | hp2 | a0002 | c0002 | t0005 | g0159 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0037 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02683 | hp2 | a0001 | c0001 | t0017 | g0135 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0177 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0171 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02723 | hp1 | a0002 | c0002 | t0008 | g0127 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02738 | hp1 | a0002 | c0002 | t0011 | g0050 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02886 | hp2 | a0003 | c0003 | t0007 | g0164 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02897 | hp1 | a0003 | c0003 | t0007 | g0184 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0161 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02976 | hp2 | a0003 | c0003 | t0007 | g0174 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03098 | hp2 | a0002 | c0002 | t0019 | g0185 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03486 | hp1 | a0002 | c0002 | t0008 | g0162 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03486 | hp2 | a0002 | c0002 | t0012 | g0074 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0066 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | GWD | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03579 | hp2 | a0003 | c0003 | t0007 | g0163 | AFR | MSL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0084 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03704 | hp1 | a0001 | c0004 | t0001 | g0218 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG03834 | hp2 | a0002 | c0002 | t0011 | g0080 | SAS | BEB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG04115 | hp1 | a0002 | c0002 | t0002 | g0065 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | BEB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | STU | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0173 | AFR | YRI | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18906 | hp2 | a0002 | c0002 | t0008 | g0167 | AFR | YRI | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18948 | hp2 | a0002 | c0002 | t0004 | g0036 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18952 | hp1 | a0001 | c0005 | t0001 | g0246 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18952 | hp2 | a0002 | c0002 | t0004 | g0140 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18959 | hp1 | a0004 | c0008 | t0001 | g0193 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18964 | hp2 | a0002 | c0002 | t0006 | g0117 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18971 | hp2 | a0002 | c0002 | t0004 | g0130 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18984 | hp2 | a0001 | c0001 | t0013 | g0115 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18991 | hp1 | a0002 | c0002 | t0004 | g0035 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA18999 | hp2 | a0002 | c0002 | t0004 | g0141 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19007 | hp2 | a0001 | c0001 | t0010 | g0110 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19043 | hp1 | a0002 | c0002 | t0006 | g0170 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19057 | hp2 | a0002 | c0002 | t0004 | g0045 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19060 | hp1 | a0001 | c0005 | t0001 | g0245 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19066 | hp1 | a0001 | c0007 | t0001 | g0224 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19067 | hp2 | a0001 | c0006 | t0001 | g0249 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19076 | hp1 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19082 | hp1 | a0002 | c0002 | t0004 | g0083 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19087 | hp1 | a0002 | c0002 | t0004 | g0121 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19087 | hp2 | a0001 | c0001 | t0018 | g0009 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19091 | hp1 | a0002 | c0002 | t0004 | g0044 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | GIH | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0148 | SAS | GIH | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0081 | AMR | CLM | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02109 | hp1 | a0002 | c0002 | t0006 | g0175 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02559 | hp1 | a0002 | c0002 | t0002 | g0176 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG02559 | hp2 | a0002 | c0002 | t0012 | g0046 | AFR | ACB | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG06807 | hp1 | a0003 | c0003 | t0007 | g0165 | AFR | USA | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
HG06807 | hp2 | a0002 | c0002 | t0008 | g0168 | AFR | USA | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0178 | AFR | USA | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | USA | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0014 | REF | REF | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
homoSapiens | grch38p0 | a0002 | c0002 | t0008 | g0169 | REF | REF | GPD2_chr2_156431379_156591403 | GPD2 | chr2 | 156431379 | 156591403 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:156476190 | C | T | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.85C>T | p.His29Tyr | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/17 | 228/5812 | 85/2184 | 29/727 | chr2 | 156476190 | |||
chr2:156549737 | G | A | 2 | a0001 a0004 |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
missense_variant | MODERATE | c.791G>A | p.Arg264His | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/17 | 934/5812 | 791/2184 | 264/727 | chr2 | 156549737 | |||
chr2:156569419 | A | C | 1 | a0003 | 8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
missense_variant | MODERATE | c.1357A>C | p.Lys453Gln | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 11/17 | 1500/5812 | 1357/2184 | 453/727 | chr2 | 156569419 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:156513495 | C | T | 1 | a0001c0007 | 1 | NA19066.hp1 | splice_region_variant&synonymous_variant | LOW | c.660C>T | p.Asp220Asp | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/17 | 803/5812 | 660/2184 | 220/727 | chr2 | 156513495 | |||
chr2:156549675 | A | G | 1 | a0001c0005 | 2 | NA18952.hp1 NA19060.hp1 |
synonymous_variant | LOW | c.729A>G | p.Thr243Thr | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/17 | 872/5812 | 729/2184 | 243/727 | chr2 | 156549675 | |||
chr2:156569460 | G | A | 1 | a0001c0004 | 3 | HG00140.hp2 HG01433.hp1 HG03704.hp1 |
synonymous_variant | LOW | c.1398G>A | p.Gly466Gly | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 11/17 | 1541/5812 | 1398/2184 | 466/727 | chr2 | 156569460 | |||
chr2:156571286 | G | A | 1 | a0001c0006 | 1 | NA19067.hp2 | synonymous_variant | LOW | c.1761G>A | p.Lys587Lys | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/17 | 1904/5812 | 1761/2184 | 587/727 | chr2 | 156571286 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:156436387 | G | T | 1 | a0002c0002t0004 | 11 | HG00438.hp2 HG00621.hp1 NA18948.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-135G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/17 | 39719 | chr2 | 156436387 | ||||||
chr2:156436417 | C | T | 1 | a0002c0002t0021 | 1 | HG02074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-105C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/17 | 39689 | chr2 | 156436417 | ||||||
chr2:156583078 | G | C | 1 | a0001c0001t0013 | 2 | HG02523.hp2 NA18984.hp2 |
3_prime_UTR_variant | MODIFIER | c.*160G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 160 | chr2 | 156583078 | ||||||
chr2:156583140 | C | T | 1 | a0002c0002t0020 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*222C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 222 | chr2 | 156583140 | ||||||
chr2:156583345 | A | G | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(25): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*427A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 427 | chr2 | 156583345 | ||||||
chr2:156583401 | A | G | 1 | a0002c0002t0012 | 3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*483A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 483 | chr2 | 156583401 | ||||||
chr2:156583657 | C | G | 1 | a0002c0002t0011 | 3 | HG01496.hp2 HG02738.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*739C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 739 | chr2 | 156583657 | ||||||
chr2:156584007 | C | A | 1 | a0001c0001t0015 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1089C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1089 | chr2 | 156584007 | ||||||
chr2:156584132 | G | C | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0010 others(12): Show |
169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1214G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1214 | chr2 | 156584132 | ||||||
chr2:156584454 | A | G | 1 | a0002c0002t0019 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1536A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1536 | chr2 | 156584454 | ||||||
chr2:156584584 | G | T | 1 | a0001c0001t0018 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1666G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1666 | chr2 | 156584584 | ||||||
chr2:156584597 | C | T | 1 | a0003c0003t0007 | 7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1679C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1679 | chr2 | 156584597 | ||||||
chr2:156584789 | A | G | 1 | a0001c0001t0010 | 4 | HG00438.hp1 HG02071.hp2 NA19007.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1871A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 1871 | chr2 | 156584789 | ||||||
chr2:156585152 | G | C | 9 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0006 others(6): Show |
63 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2234G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2234 | chr2 | 156585152 | ||||||
chr2:156585158 | A | G | 1 | a0002c0002t0014 | 2 | HG01070.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2240A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2240 | chr2 | 156585158 | ||||||
chr2:156585291 | C | T | 2 | a0002c0002t0006 a0002c0002t0019 |
9 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2373C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2373 | chr2 | 156585291 | ||||||
chr2:156585613 | G | C | 1 | a0001c0001t0016 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2695G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2695 | chr2 | 156585613 | ||||||
chr2:156585725 | G | A | 1 | a0002c0002t0009 | 5 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2807G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2807 | chr2 | 156585725 | ||||||
chr2:156585741 | G | A | 9 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0006 others(6): Show |
63 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2823G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 2823 | chr2 | 156585741 | ||||||
chr2:156586242 | CTG | C | 2 | a0001c0001t0003 a0001c0001t0018 |
19 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3328_*3329delGT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 3328 | INFO_REALIGN_3_PRIME | chr2 | 156586242 | |||||
chr2:156586245 | T | G | 1 | a0001c0001t0017 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3327T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 17/17 | 3327 | chr2 | 156586245 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:156436560 | G | C | 11 | a0001c0001t0001g0003 a0001c0001t0003g0001 a0001c0001t0003g0002 others(8): Show |
11 | HG00558.hp1 HG02015.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+47G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156436560 | |||||||
chr2:156436561 | G | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-9+48G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156436561 | |||||||
chr2:156436627 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-9+114C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156436627 | |||||||
chr2:156437434 | A | C | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-9+921A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156437434 | |||||||
chr2:156437479 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+966A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156437479 | |||||||
chr2:156437527 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+1014C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156437527 | |||||||
chr2:156437595 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-9+1082C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156437595 | |||||||
chr2:156438037 | T | G | 1 | a0003c0003t0007g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9+1524T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156438037 | |||||||
chr2:156438432 | T | A | 146 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-9+1919T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156438432 | |||||||
chr2:156438915 | G | A | 1 | a0002c0002t0002g0013 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-9+2402G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156438915 | |||||||
chr2:156439136 | G | A | 146 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-9+2623G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439136 | |||||||
chr2:156439474 | T | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-9+2961T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439474 | |||||||
chr2:156439513 | G | GA | 19 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(16): Show |
19 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.-9+3026dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439513 | ||||||
chr2:156439513 | G | GAAA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(3): Show |
6 | HG01358.hp2 HG01517.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+3024_-9+3026dup others(3): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439513 | ||||||
chr2:156439513 | G | GAAAA | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(2): Show |
5 | HG00735.hp2 HG00741.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9+3023_-9+3026dup others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439513 | ||||||
chr2:156439517 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-9+3018_-9+3040del others(23): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439517 | ||||||
chr2:156439518 | AAAAAAAA others(15): Show |
A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+3019_-9+3040del others(22): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439518 | ||||||
chr2:156439519 | AAAAAAAA others(14): Show |
A | 1 | a0002c0002t0001g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-9+3020_-9+3040del others(21): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439519 | ||||||
chr2:156439520 | AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0005g0055 a0002c0002t0012g0075 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-9+3021_-9+3040del others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439520 | ||||||
chr2:156439522 | AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0001g0056 a0002c0002t0001g0183 |
2 | NA18950.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-9+3023_-9+3040del others(18): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439522 | ||||||
chr2:156439523 | AAAAAAAA others(10): Show |
A | 4 | a0002c0002t0006g0154 a0002c0002t0006g0155 a0002c0002t0006g0156 others(1): Show |
4 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+3024_-9+3040del others(17): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439523 | ||||||
chr2:156439524 | AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0058 a0002c0002t0002g0065 |
2 | HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-9+3025_-9+3040del others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439524 | ||||||
chr2:156439525 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0010g0110 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-9+3026_-9+3040del others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439525 | ||||||
chr2:156439528 | A | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+3015A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439528 | |||||||
chr2:156439529 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-9+3027_-9+3037del others(11): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439529 | ||||||
chr2:156439530 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-9+3027_-9+3036del others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439530 | ||||||
chr2:156439535 | AAAAAC | A | 8 | a0001c0001t0001g0234 a0001c0001t0003g0001 a0001c0001t0003g0004 others(5): Show |
8 | HG00558.hp1 HG02015.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3027_-9+3031del others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439535 | ||||||
chr2:156439536 | A | C | 1 | a0001c0001t0001g0107 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-9+3023A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439536 | |||||||
chr2:156439536 | AAAAC | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0145 others(6): Show |
9 | HG01256.hp1 HG02056.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+3027_-9+3030del others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439536 | ||||||
chr2:156439537 | AAAC | A | 23 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(20): Show |
23 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9+3027_-9+3029del others(3): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439537 | ||||||
chr2:156439538 | AAC | A | 51 | a0001c0001t0001g0040 a0001c0001t0001g0077 a0001c0001t0001g0102 others(48): Show |
51 | HG00323.hp1 HG00544.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.-9+3027_-9+3028del others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439538 | ||||||
chr2:156439539 | AC | A | 60 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0047 others(57): Show |
60 | HG00621.hp2 HG00639.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.-9+3027delC | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439539 | |||||||
chr2:156439540 | C | A | 68 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(65): Show |
68 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-9+3027C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439540 | |||||||
chr2:156439541 | A | C | 3 | a0002c0002t0002g0152 a0002c0002t0005g0159 a0002c0002t0019g0185 |
3 | HG01358.hp1 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-9+3028A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439541 | |||||||
chr2:156439620 | G | A | 1 | a0001c0001t0003g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-9+3107G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439620 | |||||||
chr2:156439744 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-9+3231G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439744 | |||||||
chr2:156439849 | A | AAAATAAA others(1): Show |
135 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(132): Show |
135 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.-9+3356_-9+3363dup others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439849 | ||||||
chr2:156439849 | A | AAAATAAA others(5): Show |
20 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0143 others(17): Show |
20 | HG01243.hp1 HG01258.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-9+3352_-9+3363dup others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439849 | ||||||
chr2:156439849 | A | AAAATAAA others(9): Show |
62 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0192 others(59): Show |
62 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-9+3348_-9+3363dup others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439849 | ||||||
chr2:156439849 | A | AAAATAAA others(13): Show |
8 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0247 others(5): Show |
8 | HG02698.hp1 HG02818.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+3344_-9+3363dup others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439849 | ||||||
chr2:156439849 | A | AAAATAAA others(17): Show |
1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+3340_-9+3363dup others(24): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156439849 | ||||||
chr2:156439935 | A | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | NA19006.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-9+3422A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156439935 | |||||||
chr2:156440221 | C | T | 1 | a0001c0001t0003g0240 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-9+3708C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440221 | |||||||
chr2:156440264 | A | C | 1 | a0002c0002t0009g0137 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-9+3751A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440264 | |||||||
chr2:156440273 | A | G | 9 | a0001c0001t0005g0180 a0002c0002t0001g0181 a0002c0002t0001g0182 others(6): Show |
9 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+3760A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440273 | |||||||
chr2:156440466 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9+3953G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440466 | |||||||
chr2:156440647 | A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+4134A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440647 | |||||||
chr2:156440679 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-9+4166A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156440679 | |||||||
chr2:156441010 | C | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(238): Show |
241 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9+4497C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441010 | |||||||
chr2:156441339 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-9+4826C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441339 | |||||||
chr2:156441414 | C | T | 1 | a0001c0001t0017g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-9+4901C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441414 | |||||||
chr2:156441454 | G | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+4941G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441454 | |||||||
chr2:156441669 | A | G | 146 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-9+5156A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441669 | |||||||
chr2:156441817 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-9+5304G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441817 | |||||||
chr2:156441919 | A | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
5 | HG01070.hp1 HG01192.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+5406A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441919 | |||||||
chr2:156441957 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-9+5444T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156441957 | |||||||
chr2:156442075 | G | T | 146 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-9+5562G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156442075 | |||||||
chr2:156442542 | G | T | 222 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-9+6029G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156442542 | |||||||
chr2:156442679 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+6166G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156442679 | |||||||
chr2:156442756 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+6243A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156442756 | |||||||
chr2:156443127 | C | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA19000.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-9+6614C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156443127 | |||||||
chr2:156443224 | C | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+6711C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156443224 | |||||||
chr2:156443433 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(220): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-9+6920C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156443433 | |||||||
chr2:156443526 | T | C | 3 | a0001c0001t0001g0192 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG02698.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-9+7013T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156443526 | |||||||
chr2:156443650 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-9+7137T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156443650 | |||||||
chr2:156444089 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0003g0001 a0001c0001t0003g0002 others(8): Show |
11 | HG00558.hp1 HG02015.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9+7576T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444089 | |||||||
chr2:156444110 | G | A | 143 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(140): Show |
143 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.-9+7597G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444110 | |||||||
chr2:156444133 | G | A | 2 | a0002c0002t0001g0194 a0004c0008t0001g0193 |
2 | HG02071.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-9+7620G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444133 | |||||||
chr2:156444252 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-9+7739A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444252 | |||||||
chr2:156444329 | T | C | 2 | a0002c0002t0001g0173 a0003c0003t0007g0174 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-9+7816T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444329 | |||||||
chr2:156444436 | G | C | 1 | a0001c0001t0005g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9+7923G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444436 | |||||||
chr2:156444720 | T | TAC | 153 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(150): Show |
153 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.-9+8226_-9+8227dup others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156444720 | ||||||
chr2:156444720 | T | TACAC | 3 | a0002c0002t0004g0044 a0002c0002t0004g0045 a0002c0002t0012g0046 |
3 | HG02559.hp2 NA19057.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-9+8224_-9+8227dup others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156444720 | ||||||
chr2:156444720 | T | TACACACA others(3): Show |
74 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(71): Show |
74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-9+8218_-9+8227dup others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156444720 | ||||||
chr2:156444720 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0195 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-9+8216_-9+8227dup others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156444720 | ||||||
chr2:156444846 | C | T | 1 | a0002c0002t0004g0036 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-9+8333C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444846 | |||||||
chr2:156444925 | A | G | 2 | a0002c0002t0004g0035 a0002c0002t0004g0130 |
2 | NA18971.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-9+8412A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156444925 | |||||||
chr2:156445161 | C | G | 1 | a0001c0001t0001g0235 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-9+8648C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445161 | |||||||
chr2:156445316 | T | G | 2 | a0002c0002t0004g0044 a0002c0002t0004g0045 |
2 | NA19057.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-9+8803T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445316 | |||||||
chr2:156445668 | C | T | 5 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+9155C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445668 | |||||||
chr2:156445679 | A | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(220): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-9+9166A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445679 | |||||||
chr2:156445802 | T | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+9289T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445802 | |||||||
chr2:156445879 | A | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(220): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-9+9366A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156445879 | |||||||
chr2:156446107 | A | AT | 147 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(144): Show |
147 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.-9+9602dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156446107 | ||||||
chr2:156446159 | G | A | 5 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+9646G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446159 | |||||||
chr2:156446256 | C | T | 1 | a0002c0002t0002g0129 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-9+9743C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446256 | |||||||
chr2:156446335 | G | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(220): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-9+9822G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446335 | |||||||
chr2:156446339 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9+9826G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446339 | |||||||
chr2:156446531 | A | G | 4 | a0003c0003t0007g0163 a0003c0003t0007g0164 a0003c0003t0007g0165 others(1): Show |
4 | HG02886.hp2 HG02897.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+10018A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446531 | |||||||
chr2:156446606 | G | A | 2 | a0002c0002t0001g0173 a0003c0003t0007g0174 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-9+10093G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446606 | |||||||
chr2:156446670 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-9+10157G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446670 | |||||||
chr2:156446982 | G | A | 1 | a0002c0002t0002g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-9+10469G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156446982 | |||||||
chr2:156447233 | C | T | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-9+10720C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447233 | |||||||
chr2:156447399 | A | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | NA19000.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-9+10886A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447399 | |||||||
chr2:156447498 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-9+10985T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447498 | |||||||
chr2:156447584 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-9+11071C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447584 | |||||||
chr2:156447690 | T | C | 241 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(238): Show |
241 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9+11177T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447690 | |||||||
chr2:156447934 | G | A | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG02698.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-9+11421G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447934 | |||||||
chr2:156447959 | A | G | 2 | a0001c0001t0010g0019 a0001c0001t0010g0128 |
2 | HG00438.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-9+11446A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156447959 | |||||||
chr2:156448119 | C | CT | 77 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0187 others(74): Show |
77 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-9+11619dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156448119 | ||||||
chr2:156448220 | G | T | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-9+11707G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448220 | |||||||
chr2:156448232 | C | T | 1 | a0001c0001t0005g0171 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-9+11719C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448232 | |||||||
chr2:156448269 | G | A | 146 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-9+11756G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448269 | |||||||
chr2:156448352 | C | A | 146 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-9+11839C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448352 | |||||||
chr2:156448619 | C | T | 146 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-9+12106C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448619 | |||||||
chr2:156448675 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+12162A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448675 | |||||||
chr2:156448742 | T | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(73): Show |
76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-9+12229T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448742 | |||||||
chr2:156448918 | T | G | 1 | a0001c0001t0003g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-9+12405T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156448918 | |||||||
chr2:156449218 | G | C | 146 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-9+12705G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156449218 | |||||||
chr2:156449251 | T | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+12738T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156449251 | |||||||
chr2:156449376 | T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+12863T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156449376 | |||||||
chr2:156449395 | C | A | 1 | a0001c0001t0016g0049 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-9+12882C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156449395 | |||||||
chr2:156449856 | C | CAAAAAAA others(4): Show |
1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+13345_-9+13355d others(13): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156449856 | ||||||
chr2:156449856 | C | CAAAAAAA others(5): Show |
5 | a0001c0001t0001g0126 a0002c0002t0002g0150 a0002c0002t0002g0151 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+13344_-9+13355d others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156449856 | ||||||
chr2:156449856 | C | CAAAAAAA others(6): Show |
181 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.-9+13355_-9+13356i others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156449856 | ||||||
chr2:156449856 | C | CAAAAAAA others(7): Show |
34 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0043 others(31): Show |
34 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.-9+13355_-9+13356i others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156449856 | ||||||
chr2:156450016 | GA | G | 241 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(238): Show |
241 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9+13509delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156450016 | ||||||
chr2:156450176 | A | G | 222 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-9+13663A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450176 | |||||||
chr2:156450208 | T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+13695T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450208 | |||||||
chr2:156450368 | A | G | 1 | a0001c0001t0016g0049 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-9+13855A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450368 | |||||||
chr2:156450516 | G | C | 222 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-9+14003G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450516 | |||||||
chr2:156450652 | C | G | 1 | a0002c0002t0002g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-9+14139C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450652 | |||||||
chr2:156450665 | C | CTTT | 74 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(71): Show |
74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-9+14167_-9+14169d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156450665 | ||||||
chr2:156450665 | C | CTTTT | 17 | a0001c0001t0001g0234 a0001c0001t0005g0180 a0002c0002t0001g0182 others(14): Show |
17 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9+14166_-9+14169d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156450665 | ||||||
chr2:156450682 | T | TTTA | 15 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 others(12): Show |
15 | HG01070.hp1 HG01070.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9+14169_-9+14170i others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450682 | |||||||
chr2:156450682 | T | TTTTA | 134 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(131): Show |
134 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-9+14169_-9+14170i others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450682 | |||||||
chr2:156450687 | C | A | 245 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-9+14174C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450687 | |||||||
chr2:156450707 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-9+14194G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450707 | |||||||
chr2:156450731 | C | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-9+14218C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450731 | |||||||
chr2:156450734 | G | T | 3 | a0002c0002t0002g0149 a0002c0002t0002g0150 a0002c0002t0002g0151 |
3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-9+14221G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450734 | |||||||
chr2:156450917 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+14404C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156450917 | |||||||
chr2:156451122 | G | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-9+14609G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451122 | |||||||
chr2:156451158 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0005g0160 a0001c0001t0005g0171 |
3 | HG00140.hp1 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-9+14645C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451158 | |||||||
chr2:156451183 | C | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+14670C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451183 | |||||||
chr2:156451193 | G | T | 1 | a0002c0002t0002g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-9+14680G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451193 | |||||||
chr2:156451233 | G | C | 150 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(147): Show |
150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-9+14720G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451233 | |||||||
chr2:156451241 | CGGGCAGA others(120): Show |
C | 1 | a0001c0001t0001g0195 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-9+14797_-9+14923d others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451241 | ||||||
chr2:156451296 | A | AC | 57 | a0001c0001t0001g0043 a0001c0001t0001g0187 a0001c0001t0001g0188 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.-9+14790dupC | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451296 | ||||||
chr2:156451303 | C | G | 1 | a0002c0002t0008g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-9+14790C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451303 | |||||||
chr2:156451315 | G | A | 1 | a0002c0002t0020g0021 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-9+14802G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451315 | |||||||
chr2:156451341 | TGCTCCTC others(268): Show |
T | 1 | a0002c0002t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-9+14978_-9+15252d others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451341 | ||||||
chr2:156451393 | G | A | 33 | a0001c0001t0001g0029 a0001c0001t0001g0052 a0001c0001t0001g0077 others(30): Show |
33 | HG00639.hp1 HG01070.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.-9+14880G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451393 | |||||||
chr2:156451424 | CCCCCCCA others(41): Show |
C | 1 | a0001c0001t0001g0057 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-9+14918_-9+14965d others(50): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451424 | ||||||
chr2:156451442 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0096 |
2 | NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-9+14929G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451442 | |||||||
chr2:156451447 | G | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+14934G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451447 | |||||||
chr2:156451462 | CGGGGGGC others(43): Show |
C | 146 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
146 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.-9+14978_-9+15027d others(52): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451462 | ||||||
chr2:156451473 | CCCCCCCA others(42): Show |
C | 3 | a0001c0001t0016g0049 a0002c0002t0002g0079 a0002c0002t0009g0137 |
3 | HG01261.hp1 HG01261.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-9+14967_-9+15015d others(51): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451473 | ||||||
chr2:156451491 | G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+14978G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451491 | |||||||
chr2:156451491 | GGAAGGGG others(43): Show |
G | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0197 others(2): Show |
5 | HG01993.hp2 NA19006.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+14981_-9+15030d others(52): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451491 | ||||||
chr2:156451491 | GGAAGGGG others(268): Show |
G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-9+14981_-9+15255d others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451491 | ||||||
chr2:156451494 | A | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0187 others(73): Show |
76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.-9+14981A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451494 | |||||||
chr2:156451509 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0198 |
2 | NA19006.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-9+14996A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451509 | |||||||
chr2:156451512 | G | A | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-9+14999G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451512 | |||||||
chr2:156451517 | G | A | 5 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+15004G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451517 | |||||||
chr2:156451572 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-9+15059C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451572 | |||||||
chr2:156451598 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-9+15085C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451598 | |||||||
chr2:156451717 | GGACGGGG others(42): Show |
G | 1 | a0002c0002t0002g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-9+15208_-9+15256d others(51): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451717 | ||||||
chr2:156451721 | G | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9+15208G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451721 | |||||||
chr2:156451725 | C | T | 86 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(83): Show |
86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-9+15212C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451725 | |||||||
chr2:156451731 | GCCGGGCG others(10): Show |
G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+15221_-9+15237d others(19): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156451731 | ||||||
chr2:156451766 | A | G | 224 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(221): Show |
224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.-9+15253A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451766 | |||||||
chr2:156451849 | T | C | 2 | a0002c0002t0005g0159 a0003c0003t0005g0158 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-9+15336T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451849 | |||||||
chr2:156451927 | G | C | 3 | a0001c0001t0003g0037 a0001c0001t0003g0071 a0001c0001t0003g0072 |
3 | HG02683.hp1 HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-9+15414G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451927 | |||||||
chr2:156451933 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-9+15420A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156451933 | |||||||
chr2:156452202 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-9+15689C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452202 | |||||||
chr2:156452233 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-9+15720G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452233 | |||||||
chr2:156452360 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-9+15847C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452360 | |||||||
chr2:156452434 | A | G | 2 | a0002c0002t0002g0065 a0002c0002t0002g0066 |
2 | HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-9+15921A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452434 | |||||||
chr2:156452542 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-9+16029G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452542 | |||||||
chr2:156452565 | G | A | 3 | a0002c0002t0002g0149 a0002c0002t0002g0150 a0002c0002t0002g0151 |
3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-9+16052G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156452565 | |||||||
chr2:156453377 | T | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG02735.hp1 HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-9+16864T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156453377 | |||||||
chr2:156453833 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-9+17320C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156453833 | |||||||
chr2:156453948 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-9+17435A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156453948 | |||||||
chr2:156454043 | A | G | 1 | a0002c0002t0002g0122 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-9+17530A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156454043 | |||||||
chr2:156454150 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-9+17637G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156454150 | |||||||
chr2:156454256 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-9+17743T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156454256 | |||||||
chr2:156454493 | G | GA | 92 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(89): Show |
92 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.-9+17991dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156454493 | ||||||
chr2:156454493 | G | GAA | 52 | a0001c0001t0001g0029 a0001c0001t0001g0052 a0001c0001t0001g0077 others(49): Show |
52 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.-9+17990_-9+17991d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156454493 | ||||||
chr2:156454539 | T | C | 1 | a0001c0001t0005g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-9+18026T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156454539 | |||||||
chr2:156455005 | A | G | 1 | a0002c0002t0008g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-9+18492A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455005 | |||||||
chr2:156455216 | C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+18703C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455216 | |||||||
chr2:156455310 | T | C | 3 | a0001c0001t0001g0196 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG00323.hp1 HG01106.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-9+18797T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455310 | |||||||
chr2:156455337 | G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+18824G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455337 | |||||||
chr2:156455635 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-9+19122A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455635 | |||||||
chr2:156455713 | G | T | 4 | a0002c0002t0002g0020 a0002c0002t0002g0089 a0002c0002t0002g0090 others(1): Show |
4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+19200G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455713 | |||||||
chr2:156455759 | GT | G | 225 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-9+19249delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156455759 | ||||||
chr2:156455892 | T | C | 2 | a0002c0002t0001g0173 a0003c0003t0007g0174 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-9+19379T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156455892 | |||||||
chr2:156456023 | A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+19510A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156456023 | |||||||
chr2:156456436 | T | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.-8-19662T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156456436 | |||||||
chr2:156456472 | G | A | 1 | a0003c0003t0007g0063 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-8-19626G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156456472 | |||||||
chr2:156456586 | A | T | 1 | a0002c0002t0004g0045 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-8-19512A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156456586 | |||||||
chr2:156456595 | C | CA | 5 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-19490dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156456595 | ||||||
chr2:156457081 | T | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-19017T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156457081 | |||||||
chr2:156457357 | G | A | 1 | a0002c0002t0012g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-8-18741G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156457357 | |||||||
chr2:156457674 | C | G | 1 | a0001c0001t0005g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-8-18424C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156457674 | |||||||
chr2:156458487 | A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-17611A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156458487 | |||||||
chr2:156458858 | C | T | 1 | a0001c0001t0003g0088 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-8-17240C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156458858 | |||||||
chr2:156458909 | C | T | 3 | a0001c0001t0001g0248 a0001c0001t0001g0250 a0001c0006t0001g0249 |
3 | NA18945.hp2 NA18983.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-8-17189C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156458909 | |||||||
chr2:156458912 | T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-17186T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156458912 | |||||||
chr2:156459006 | A | AAT | 8 | a0002c0002t0001g0181 a0002c0002t0001g0183 a0002c0002t0002g0161 others(5): Show |
8 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-17072_-8-17071d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459006 | ||||||
chr2:156459006 | AAT | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(71): Show |
74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-8-17072_-8-17071d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459006 | ||||||
chr2:156459006 | AATAT | A | 3 | a0001c0001t0001g0234 a0002c0002t0004g0044 a0002c0002t0004g0045 |
3 | HG02451.hp2 NA19057.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-8-17074_-8-17071d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459006 | ||||||
chr2:156459006 | AATATAT | A | 149 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(146): Show |
149 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.-8-17076_-8-17071d others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459006 | ||||||
chr2:156459026 | T | C | 2 | a0001c0001t0005g0180 a0002c0002t0005g0159 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-17072T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459026 | |||||||
chr2:156459236 | G | T | 50 | a0001c0001t0001g0029 a0001c0001t0001g0052 a0001c0001t0001g0077 others(47): Show |
50 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-8-16862G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459236 | |||||||
chr2:156459292 | A | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-16806A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459292 | |||||||
chr2:156459493 | T | C | 5 | a0001c0001t0005g0180 a0003c0003t0007g0163 a0003c0003t0007g0164 others(2): Show |
5 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-16605T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459493 | |||||||
chr2:156459569 | T | G | 3 | a0002c0002t0001g0173 a0002c0002t0019g0185 a0003c0003t0007g0174 |
3 | HG02976.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8-16529T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459569 | |||||||
chr2:156459603 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0003g0001 |
2 | NA18970.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-8-16495G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459603 | |||||||
chr2:156459672 | G | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-16426G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459672 | |||||||
chr2:156459682 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | NA18941.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-8-16416G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156459682 | |||||||
chr2:156459686 | C | CAAA | 11 | a0001c0001t0001g0062 a0001c0001t0001g0209 a0001c0001t0001g0210 others(8): Show |
11 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-16391_-8-16389d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAA | 60 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(57): Show |
60 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8-16392_-8-16389d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAA | 20 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0214 others(17): Show |
20 | HG00621.hp2 HG00741.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-16393_-8-16389d others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA | 10 | a0001c0001t0005g0160 a0001c0001t0005g0166 a0001c0001t0005g0171 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-16395_-8-16389d others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA others(2): Show |
5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
5 | HG00438.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-16397_-8-16389d others(11): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA others(3): Show |
5 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0001g0123 others(2): Show |
5 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-16398_-8-16389d others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA others(4): Show |
19 | a0001c0001t0001g0023 a0001c0001t0001g0131 a0001c0001t0001g0134 others(16): Show |
19 | HG01070.hp1 HG01070.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-16399_-8-16389d others(13): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA others(5): Show |
46 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0029 others(43): Show |
46 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8-16400_-8-16389d others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA others(6): Show |
28 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(25): Show |
28 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-8-16401_-8-16389d others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA others(7): Show |
21 | a0001c0001t0001g0026 a0001c0001t0001g0058 a0001c0001t0001g0059 others(18): Show |
21 | HG00323.hp2 HG00639.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8-16402_-8-16389d others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0057 a0002c0002t0012g0046 |
2 | HG02559.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-8-16403_-8-16389d others(17): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0076 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-16404_-8-16389d others(18): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0056 a0001c0001t0001g0094 |
2 | HG04184.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.-8-16405_-8-16389d others(19): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0003g0071 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8-16411_-8-16389d others(25): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156459686 | CAAAAAAA others(3): Show |
C | 8 | a0001c0001t0001g0038 a0002c0002t0009g0034 a0002c0002t0009g0118 others(5): Show |
8 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-8-16398_-8-16389d others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156459686 | ||||||
chr2:156460129 | A | C | 3 | a0002c0002t0001g0173 a0002c0002t0019g0185 a0003c0003t0007g0174 |
3 | HG02976.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8-15969A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460129 | |||||||
chr2:156460241 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-8-15857C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460241 | |||||||
chr2:156460241 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-8-15857C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460241 | |||||||
chr2:156460564 | T | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-8-15534T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460564 | |||||||
chr2:156460574 | G | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-8-15524G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460574 | |||||||
chr2:156460574 | G | T | 1 | a0001c0001t0003g0001 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-8-15524G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460574 | |||||||
chr2:156460645 | T | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-15453T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460645 | |||||||
chr2:156460680 | A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-15418A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460680 | |||||||
chr2:156460740 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-8-15358G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460740 | |||||||
chr2:156460952 | T | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-15146T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156460952 | |||||||
chr2:156461033 | T | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(2): Show |
5 | HG02630.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-15065T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461033 | |||||||
chr2:156461161 | C | CT | 6 | a0001c0001t0005g0160 a0002c0002t0001g0182 a0002c0002t0001g0183 others(3): Show |
6 | HG02886.hp2 HG02897.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-14912dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156461161 | ||||||
chr2:156461161 | CT | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(68): Show |
71 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-8-14912delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156461161 | ||||||
chr2:156461161 | CTTTTTTT others(1): Show |
C | 87 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(84): Show |
87 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-8-14919_-8-14912d others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156461161 | ||||||
chr2:156461161 | CTTTTTTT others(2): Show |
C | 61 | a0001c0001t0001g0029 a0001c0001t0001g0052 a0001c0001t0001g0062 others(58): Show |
61 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-8-14920_-8-14912d others(11): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156461161 | ||||||
chr2:156461161 | CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0002g0151 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-8-14921_-8-14912d others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156461161 | ||||||
chr2:156461303 | A | G | 150 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(147): Show |
150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-8-14795A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461303 | |||||||
chr2:156461430 | C | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-14668C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461430 | |||||||
chr2:156461580 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-8-14518A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461580 | |||||||
chr2:156461646 | C | T | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-14452C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461646 | |||||||
chr2:156461915 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-8-14183G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156461915 | |||||||
chr2:156462354 | C | T | 5 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-13744C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462354 | |||||||
chr2:156462379 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(158): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-8-13719G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462379 | |||||||
chr2:156462386 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-8-13712A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462386 | |||||||
chr2:156462435 | A | G | 1 | a0002c0002t0008g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8-13663A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462435 | |||||||
chr2:156462453 | A | AT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0093 others(6): Show |
9 | HG00741.hp2 HG01109.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8-13625dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156462453 | ||||||
chr2:156462453 | AT | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(69): Show |
72 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-8-13625delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156462453 | ||||||
chr2:156462674 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG02602.hp2 NA18941.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.-8-13424G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462674 | |||||||
chr2:156462733 | GA | G | 4 | a0002c0002t0006g0154 a0002c0002t0006g0155 a0002c0002t0006g0156 others(1): Show |
4 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-13363delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156462733 | ||||||
chr2:156462748 | G | C | 1 | a0002c0002t0006g0117 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-8-13350G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462748 | |||||||
chr2:156462864 | G | C | 1 | a0001c0001t0001g0192 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-13234G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156462864 | |||||||
chr2:156463416 | A | G | 5 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-12682A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463416 | |||||||
chr2:156463421 | A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-12677A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463421 | |||||||
chr2:156463510 | T | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-12588T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463510 | |||||||
chr2:156463543 | T | G | 3 | a0002c0002t0004g0121 a0002c0002t0004g0140 a0002c0002t0004g0141 |
3 | NA18952.hp2 NA18999.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-8-12555T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463543 | |||||||
chr2:156463580 | C | T | 1 | a0002c0002t0009g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-8-12518C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463580 | |||||||
chr2:156463598 | G | A | 1 | a0002c0002t0002g0084 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-8-12500G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463598 | |||||||
chr2:156463646 | G | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-12452G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463646 | |||||||
chr2:156463682 | C | T | 85 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(82): Show |
85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-8-12416C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463682 | |||||||
chr2:156463692 | C | A | 3 | a0001c0004t0001g0199 a0001c0004t0001g0218 a0001c0004t0001g0219 |
3 | HG00140.hp2 HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-8-12406C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463692 | |||||||
chr2:156463692 | C | G | 9 | a0001c0001t0005g0180 a0002c0002t0001g0181 a0002c0002t0001g0182 others(6): Show |
9 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-12406C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463692 | |||||||
chr2:156463749 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-8-12349A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463749 | |||||||
chr2:156463825 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-8-12273C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463825 | |||||||
chr2:156463904 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-12194A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156463904 | |||||||
chr2:156464189 | C | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-11909C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464189 | |||||||
chr2:156464262 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0145 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-8-11836T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464262 | |||||||
chr2:156464380 | T | G | 5 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-11718T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464380 | |||||||
chr2:156464486 | A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-11612A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464486 | |||||||
chr2:156464772 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-8-11326A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464772 | |||||||
chr2:156464828 | C | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-11270C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156464828 | |||||||
chr2:156465169 | A | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-10929A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465169 | |||||||
chr2:156465180 | C | T | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-10918C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465180 | |||||||
chr2:156465272 | TAA | T | 150 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(147): Show |
150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.-8-10825_-8-10824d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465272 | |||||||
chr2:156465361 | CT | C | 157 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(154): Show |
157 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.-8-10719delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156465361 | ||||||
chr2:156465361 | CTT | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0001t0001g0077 others(3): Show |
6 | HG02523.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-10720_-8-10719d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156465361 | ||||||
chr2:156465362 | T | TTTC | 75 | a0001c0001t0001g0003 a0001c0001t0001g0093 a0001c0001t0001g0187 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-10734_-8-10733i others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156465362 | ||||||
chr2:156465365 | T | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0124 a0001c0001t0005g0055 others(3): Show |
6 | HG00140.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-10733T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465365 | |||||||
chr2:156465366 | T | C | 138 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(135): Show |
138 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.-8-10732T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465366 | |||||||
chr2:156465367 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0001t0001g0077 others(2): Show |
5 | HG02523.hp2 HG02897.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-10731T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465367 | |||||||
chr2:156465559 | C | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-8-10539C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465559 | |||||||
chr2:156465621 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-10477G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465621 | |||||||
chr2:156465759 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-8-10339A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465759 | |||||||
chr2:156465820 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-8-10278T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465820 | |||||||
chr2:156465867 | A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-10231A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156465867 | |||||||
chr2:156466048 | G | C | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-10050G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156466048 | |||||||
chr2:156466330 | G | A | 2 | a0002c0002t0002g0085 a0002c0002t0021g0054 |
2 | HG01106.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.-8-9768G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156466330 | |||||||
chr2:156466460 | G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-9638G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156466460 | |||||||
chr2:156466792 | T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-9306T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156466792 | |||||||
chr2:156467096 | A | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-9002A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467096 | |||||||
chr2:156467174 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-8-8924G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467174 | |||||||
chr2:156467476 | T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-8622T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467476 | |||||||
chr2:156467494 | T | C | 1 | a0002c0002t0001g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-8-8604T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467494 | |||||||
chr2:156467500 | G | C | 1 | a0002c0002t0001g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-8-8598G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467500 | |||||||
chr2:156467640 | C | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-8458C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467640 | |||||||
chr2:156467654 | G | A | 1 | a0003c0003t0007g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-8-8444G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467654 | |||||||
chr2:156467698 | G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-8400G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467698 | |||||||
chr2:156467926 | T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-8172T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156467926 | |||||||
chr2:156468313 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0052 others(124): Show |
127 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-8-7785T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156468313 | |||||||
chr2:156468540 | CA | C | 3 | a0002c0002t0002g0149 a0002c0002t0002g0150 a0002c0002t0002g0151 |
3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-8-7554delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156468540 | ||||||
chr2:156468615 | T | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-7483T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156468615 | |||||||
chr2:156468862 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-8-7236A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156468862 | |||||||
chr2:156469478 | T | C | 3 | a0001c0004t0001g0199 a0001c0004t0001g0218 a0001c0004t0001g0219 |
3 | HG00140.hp2 HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-8-6620T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469478 | |||||||
chr2:156469525 | T | C | 2 | a0001c0001t0010g0019 a0001c0001t0010g0128 |
2 | HG00438.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-8-6573T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469525 | |||||||
chr2:156469566 | A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-6532A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469566 | |||||||
chr2:156469820 | G | A | 2 | a0002c0002t0014g0067 a0002c0002t0014g0078 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-8-6278G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469820 | |||||||
chr2:156469858 | A | G | 1 | a0002c0002t0002g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-8-6240A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469858 | |||||||
chr2:156469884 | A | C | 25 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(22): Show |
25 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8-6214A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156469884 | |||||||
chr2:156470121 | G | A | 9 | a0001c0001t0005g0180 a0002c0002t0001g0181 a0002c0002t0001g0182 others(6): Show |
9 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-5977G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156470121 | |||||||
chr2:156470164 | C | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-8-5934C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156470164 | |||||||
chr2:156470270 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8-5828T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156470270 | |||||||
chr2:156470496 | C | T | 5 | a0001c0001t0005g0180 a0003c0003t0007g0163 a0003c0003t0007g0164 others(2): Show |
5 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-5602C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156470496 | |||||||
chr2:156470929 | A | G | 1 | a0002c0002t0001g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-8-5169A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156470929 | |||||||
chr2:156471098 | G | C | 5 | a0002c0002t0009g0034 a0002c0002t0009g0118 a0002c0002t0009g0119 others(2): Show |
5 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-5000G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471098 | |||||||
chr2:156471118 | A | G | 228 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(225): Show |
228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.-8-4980A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471118 | |||||||
chr2:156471125 | A | T | 1 | a0002c0002t0002g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-8-4973A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471125 | |||||||
chr2:156471437 | T | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-4661T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471437 | |||||||
chr2:156471761 | A | G | 1 | a0002c0002t0002g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-8-4337A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471761 | |||||||
chr2:156471801 | C | T | 5 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-4297C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471801 | |||||||
chr2:156471852 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-8-4246T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471852 | |||||||
chr2:156471928 | G | T | 2 | a0002c0002t0001g0173 a0003c0003t0007g0174 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-8-4170G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156471928 | |||||||
chr2:156472068 | T | A | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-4030T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472068 | |||||||
chr2:156472189 | A | C | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-3909A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472189 | |||||||
chr2:156472191 | C | CT | 12 | a0001c0001t0005g0180 a0002c0002t0001g0181 a0002c0002t0001g0182 others(9): Show |
12 | HG01884.hp2 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-3897dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156472191 | ||||||
chr2:156472202 | G | T | 1 | a0001c0001t0001g0253 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8-3896G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472202 | |||||||
chr2:156472385 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-8-3713G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472385 | |||||||
chr2:156472435 | C | T | 2 | a0001c0001t0005g0055 a0002c0002t0012g0075 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-8-3663C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472435 | |||||||
chr2:156472448 | G | C | 1 | a0002c0002t0006g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8-3650G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472448 | |||||||
chr2:156472465 | C | T | 7 | a0001c0001t0001g0062 a0002c0002t0006g0039 a0002c0002t0006g0117 others(4): Show |
7 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-3633C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472465 | |||||||
chr2:156472592 | G | T | 4 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0235 others(1): Show |
4 | HG04199.hp2 NA18975.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-3506G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472592 | |||||||
chr2:156472617 | C | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-3481C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472617 | |||||||
chr2:156472646 | T | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0145 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-8-3452T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156472646 | |||||||
chr2:156473172 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-8-2926T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156473172 | |||||||
chr2:156473373 | A | G | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-8-2725A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156473373 | |||||||
chr2:156473823 | T | C | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-2275T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156473823 | |||||||
chr2:156473961 | CA | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.-8-2134delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 156473961 | ||||||
chr2:156474367 | G | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-1731G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474367 | |||||||
chr2:156474471 | G | A | 3 | a0002c0002t0002g0030 a0002c0002t0002g0079 a0002c0002t0002g0084 |
3 | HG01261.hp1 HG02602.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-8-1627G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474471 | |||||||
chr2:156474626 | G | A | 1 | a0001c0004t0001g0199 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-8-1472G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474626 | |||||||
chr2:156474641 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-8-1457C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474641 | |||||||
chr2:156474648 | A | T | 7 | a0001c0001t0001g0233 a0001c0001t0001g0247 a0001c0001t0001g0248 others(4): Show |
7 | NA18945.hp2 NA18952.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-1450A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474648 | |||||||
chr2:156474847 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-8-1251G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474847 | |||||||
chr2:156474870 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-8-1228C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474870 | |||||||
chr2:156474891 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-8-1207G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156474891 | |||||||
chr2:156475308 | C | T | 7 | a0002c0002t0009g0034 a0002c0002t0009g0118 a0002c0002t0009g0119 others(4): Show |
7 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-790C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475308 | |||||||
chr2:156475411 | C | G | 11 | a0001c0001t0001g0003 a0001c0001t0003g0001 a0001c0001t0003g0002 others(8): Show |
11 | HG00558.hp1 HG02015.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-687C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475411 | |||||||
chr2:156475485 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-8-613C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475485 | |||||||
chr2:156475539 | T | C | 1 | a0002c0002t0006g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8-559T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475539 | |||||||
chr2:156475728 | A | G | 1 | a0002c0002t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-8-370A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475728 | |||||||
chr2:156475729 | G | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-369G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475729 | |||||||
chr2:156475781 | C | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-8-317C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475781 | |||||||
chr2:156475816 | A | T | 1 | a0001c0001t0005g0160 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8-282A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475816 | |||||||
chr2:156475957 | G | C | 3 | a0002c0002t0009g0118 a0002c0002t0009g0119 a0002c0002t0009g0120 |
3 | HG01346.hp2 HG01433.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.-8-141G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 1/16 | chr2 | 156475957 | |||||||
chr2:156476387 | C | A | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.102+180C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156476387 | |||||||
chr2:156476735 | A | C | 4 | a0002c0002t0002g0020 a0002c0002t0002g0089 a0002c0002t0002g0090 others(1): Show |
4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+528A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156476735 | |||||||
chr2:156476736 | A | G | 151 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(148): Show |
151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.102+529A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156476736 | |||||||
chr2:156477015 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.102+808T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156477015 | |||||||
chr2:156477417 | A | G | 245 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.102+1210A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156477417 | |||||||
chr2:156477717 | G | A | 2 | a0002c0002t0006g0039 a0002c0002t0006g0117 |
2 | HG00673.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.102+1510G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156477717 | |||||||
chr2:156477886 | A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+1679A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156477886 | |||||||
chr2:156477956 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.102+1749C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156477956 | |||||||
chr2:156478004 | A | G | 1 | a0002c0002t0019g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.102+1797A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478004 | |||||||
chr2:156478097 | T | A | 1 | a0002c0002t0002g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.102+1890T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478097 | |||||||
chr2:156478350 | A | T | 150 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(147): Show |
150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.102+2143A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478350 | |||||||
chr2:156478443 | A | T | 1 | a0001c0001t0003g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.102+2236A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478443 | |||||||
chr2:156478469 | T | TA | 3 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0102 |
3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.102+2263dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156478469 | ||||||
chr2:156478488 | A | G | 1 | a0002c0002t0009g0137 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.102+2281A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478488 | |||||||
chr2:156478573 | A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.102+2366A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478573 | |||||||
chr2:156478648 | G | A | 1 | a0001c0001t0003g0001 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.102+2441G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478648 | |||||||
chr2:156478777 | G | A | 3 | a0002c0002t0001g0173 a0002c0002t0019g0185 a0003c0003t0007g0174 |
3 | HG02976.hp2 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.102+2570G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478777 | |||||||
chr2:156478785 | A | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+2578A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478785 | |||||||
chr2:156478850 | G | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+2643G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156478850 | |||||||
chr2:156479104 | T | G | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.102+2897T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479104 | |||||||
chr2:156479114 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.102+2907G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479114 | |||||||
chr2:156479179 | T | C | 1 | a0001c0001t0001g0241 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.102+2972T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479179 | |||||||
chr2:156479224 | A | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0214 |
2 | HG00741.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.102+3017A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479224 | |||||||
chr2:156479227 | A | T | 1 | a0002c0002t0002g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.102+3020A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479227 | |||||||
chr2:156479267 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.102+3060G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479267 | |||||||
chr2:156479568 | A | G | 1 | a0002c0002t0008g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102+3361A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479568 | |||||||
chr2:156479751 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.102+3544T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479751 | |||||||
chr2:156479864 | G | A | 1 | a0002c0002t0012g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.102+3657G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479864 | |||||||
chr2:156479897 | G | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.102+3690G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156479897 | |||||||
chr2:156480362 | A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+4155A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156480362 | |||||||
chr2:156480429 | G | GT | 87 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(84): Show |
87 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.102+4225dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156480429 | ||||||
chr2:156480631 | TGGCTTTG | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.102+4432_102+4438d others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156480631 | ||||||
chr2:156480694 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.102+4487G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156480694 | |||||||
chr2:156480774 | C | CT | 9 | a0001c0001t0001g0052 a0001c0001t0005g0180 a0001c0006t0001g0249 others(6): Show |
9 | HG01891.hp2 HG02622.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.102+4584dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156480774 | ||||||
chr2:156481079 | C | T | 1 | a0003c0003t0007g0165 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.102+4872C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481079 | |||||||
chr2:156481248 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.102+5041G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481248 | |||||||
chr2:156481385 | T | C | 2 | a0002c0002t0006g0039 a0002c0002t0006g0117 |
2 | HG00673.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.102+5178T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481385 | |||||||
chr2:156481486 | C | CA | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+5281dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156481486 | ||||||
chr2:156481606 | G | C | 1 | a0001c0001t0001g0188 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.102+5399G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481606 | |||||||
chr2:156481650 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.102+5443T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481650 | |||||||
chr2:156481815 | T | G | 1 | a0001c0001t0001g0241 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.102+5608T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481815 | |||||||
chr2:156481874 | G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+5667G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481874 | |||||||
chr2:156481899 | C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+5692C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481899 | |||||||
chr2:156481974 | T | C | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.102+5767T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156481974 | |||||||
chr2:156482054 | T | C | 4 | a0002c0002t0006g0154 a0002c0002t0006g0155 a0002c0002t0006g0156 others(1): Show |
4 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+5847T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482054 | |||||||
chr2:156482115 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.102+5908C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482115 | |||||||
chr2:156482140 | T | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+5933T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482140 | |||||||
chr2:156482166 | C | T | 1 | a0002c0002t0002g0053 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.102+5959C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482166 | |||||||
chr2:156482413 | G | A | 1 | a0001c0001t0016g0049 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.102+6206G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482413 | |||||||
chr2:156482500 | GGA | G | 4 | a0002c0002t0002g0020 a0002c0002t0002g0089 a0002c0002t0002g0090 others(1): Show |
4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+6294_102+6295d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482500 | |||||||
chr2:156482658 | G | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.102+6451G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482658 | |||||||
chr2:156482721 | C | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+6514C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156482721 | |||||||
chr2:156483286 | C | T | 1 | a0002c0002t0001g0182 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.102+7079C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156483286 | |||||||
chr2:156483386 | A | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+7179A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156483386 | |||||||
chr2:156483460 | C | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+7253C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156483460 | |||||||
chr2:156483663 | T | A | 53 | a0001c0001t0001g0029 a0001c0001t0001g0052 a0001c0001t0001g0077 others(50): Show |
53 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.102+7456T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156483663 | |||||||
chr2:156483848 | T | A | 1 | a0001c0001t0003g0005 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.102+7641T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156483848 | |||||||
chr2:156483987 | CT | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0052 others(111): Show |
114 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.102+7804delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156483987 | ||||||
chr2:156483987 | CTT | C | 98 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(95): Show |
98 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.102+7803_102+7804d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156483987 | ||||||
chr2:156484204 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+7997G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484204 | |||||||
chr2:156484227 | C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+8020C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484227 | |||||||
chr2:156484388 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.102+8181C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484388 | |||||||
chr2:156484407 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+8200G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484407 | |||||||
chr2:156484449 | A | G | 225 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.102+8242A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484449 | |||||||
chr2:156484472 | A | G | 6 | a0001c0001t0005g0180 a0002c0002t0008g0162 a0003c0003t0007g0163 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+8265A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484472 | |||||||
chr2:156484788 | C | T | 1 | a0002c0002t0001g0182 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.102+8581C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484788 | |||||||
chr2:156484824 | A | G | 1 | a0002c0002t0008g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102+8617A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484824 | |||||||
chr2:156484949 | A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+8742A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156484949 | |||||||
chr2:156485043 | C | G | 1 | a0001c0001t0001g0236 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.102+8836C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485043 | |||||||
chr2:156485180 | A | G | 1 | a0002c0002t0002g0030 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.102+8973A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485180 | |||||||
chr2:156485217 | T | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+9010T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485217 | |||||||
chr2:156485309 | A | G | 1 | a0002c0002t0008g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.102+9102A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485309 | |||||||
chr2:156485463 | C | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(227): Show |
230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.102+9256C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485463 | |||||||
chr2:156485637 | G | A | 7 | a0002c0002t0002g0138 a0002c0002t0006g0039 a0002c0002t0006g0117 others(4): Show |
7 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.102+9430G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485637 | |||||||
chr2:156485715 | C | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.102+9508C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485715 | |||||||
chr2:156485795 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG02895.hp1 HG02897.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.102+9588T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485795 | |||||||
chr2:156485930 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(72): Show |
75 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.102+9723G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156485930 | |||||||
chr2:156486450 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.103-9594T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156486450 | |||||||
chr2:156486677 | G | A | 2 | a0002c0002t0001g0181 a0002c0002t0001g0183 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.103-9367G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156486677 | |||||||
chr2:156487038 | G | A | 3 | a0001c0001t0001g0196 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG00323.hp1 HG01106.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.103-9006G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156487038 | |||||||
chr2:156487299 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.103-8745G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156487299 | |||||||
chr2:156487450 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.103-8594G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156487450 | |||||||
chr2:156487915 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.103-8129A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156487915 | |||||||
chr2:156488038 | G | C | 7 | a0001c0001t0001g0062 a0002c0002t0006g0039 a0002c0002t0006g0117 others(4): Show |
7 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-8006G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156488038 | |||||||
chr2:156488219 | A | G | 1 | a0002c0002t0006g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.103-7825A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156488219 | |||||||
chr2:156488405 | G | T | 1 | a0002c0002t0001g0182 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.103-7639G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156488405 | |||||||
chr2:156488761 | A | G | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103-7283A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156488761 | |||||||
chr2:156488946 | A | G | 1 | a0002c0002t0002g0030 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.103-7098A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156488946 | |||||||
chr2:156489083 | G | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG02698.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.103-6961G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489083 | |||||||
chr2:156489086 | C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.103-6958C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489086 | |||||||
chr2:156489114 | C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.103-6930C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489114 | |||||||
chr2:156489247 | T | G | 3 | a0001c0001t0001g0233 a0001c0005t0001g0245 a0001c0005t0001g0246 |
3 | NA18952.hp1 NA18969.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.103-6797T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489247 | |||||||
chr2:156489397 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.103-6647T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489397 | |||||||
chr2:156489474 | A | G | 1 | a0002c0002t0001g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-6570A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489474 | |||||||
chr2:156489687 | TCTTC | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0187 others(81): Show |
84 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.103-6322_103-6319d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489687 | ||||||
chr2:156489687 | TCTTCCTT others(1): Show |
T | 156 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(153): Show |
156 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.103-6326_103-6319d others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489687 | ||||||
chr2:156489687 | TCTTCCTT others(13): Show |
T | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.103-6338_103-6319d others(22): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489687 | ||||||
chr2:156489714 | TCCTTCCT others(13): Show |
T | 1 | a0002c0002t0002g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.103-6326_103-6307d others(22): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489714 | ||||||
chr2:156489722 | T | C | 2 | a0001c0001t0003g0011 a0002c0002t0008g0127 |
2 | HG02723.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.103-6322T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489722 | |||||||
chr2:156489722 | TCCTCCCT others(5): Show |
T | 1 | a0001c0001t0003g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.103-6305_103-6294d others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489722 | ||||||
chr2:156489730 | C | T | 1 | a0001c0001t0003g0011 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.103-6314C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489730 | |||||||
chr2:156489734 | C | T | 222 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.103-6310C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156489734 | |||||||
chr2:156489863 | TTCCTTCC others(37): Show |
T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.103-6170_103-6127d others(46): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489863 | ||||||
chr2:156489949 | A | AC | 13 | a0001c0001t0001g0052 a0001c0001t0001g0096 a0001c0001t0001g0253 others(10): Show |
13 | HG00438.hp1 HG01099.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.103-6090dupC | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156489949 | ||||||
chr2:156490034 | T | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0097 a0001c0001t0001g0104 others(3): Show |
6 | HG00544.hp1 HG02015.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-6010T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490034 | |||||||
chr2:156490185 | C | T | 1 | a0002c0002t0002g0053 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.103-5859C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490185 | |||||||
chr2:156490387 | G | GA | 81 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0029 others(78): Show |
81 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.103-5643dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156490387 | ||||||
chr2:156490387 | G | GAA | 6 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0229 others(3): Show |
6 | HG04199.hp1 HG04199.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-5644_103-5643d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156490387 | ||||||
chr2:156490402 | C | A | 5 | a0001c0001t0001g0124 a0002c0002t0002g0161 a0002c0002t0002g0177 others(2): Show |
5 | HG00140.hp1 HG02109.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5642C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490402 | |||||||
chr2:156490404 | A | T | 5 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5640A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490404 | |||||||
chr2:156490497 | G | C | 2 | a0002c0002t0001g0173 a0003c0003t0007g0174 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.103-5547G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490497 | |||||||
chr2:156490509 | C | T | 1 | a0002c0002t0019g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.103-5535C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490509 | |||||||
chr2:156490689 | C | A | 6 | a0001c0001t0001g0195 a0001c0001t0001g0201 a0001c0001t0001g0223 others(3): Show |
6 | HG00544.hp2 HG00673.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-5355C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490689 | |||||||
chr2:156490927 | GTAAAATT others(42): Show |
G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(73): Show |
76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.103-5073_103-5025d others(51): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156490927 | ||||||
chr2:156490958 | A | G | 151 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(148): Show |
151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.103-5086A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156490958 | |||||||
chr2:156491792 | G | A | 1 | a0003c0003t0007g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.103-4252G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156491792 | |||||||
chr2:156492018 | TA | T | 58 | a0001c0001t0001g0052 a0001c0001t0001g0062 a0001c0001t0001g0077 others(55): Show |
58 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.103-4011delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492018 | ||||||
chr2:156492082 | G | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.103-3962G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492082 | |||||||
chr2:156492117 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.103-3927T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492117 | |||||||
chr2:156492125 | C | G | 245 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.103-3919C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492125 | |||||||
chr2:156492147 | C | CT | 91 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0023 others(88): Show |
91 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.103-3872dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492147 | ||||||
chr2:156492147 | C | CTT | 18 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0026 others(15): Show |
18 | HG00735.hp2 HG00741.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.103-3873_103-3872d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492147 | ||||||
chr2:156492147 | CTT | C | 15 | a0001c0001t0001g0191 a0001c0001t0001g0206 a0001c0001t0001g0208 others(12): Show |
15 | HG02056.hp2 HG02698.hp1 HG02735.hp1 others(12): Show |
intron_variant | MODIFIER | c.103-3873_103-3872d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492147 | ||||||
chr2:156492147 | CTTT | C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(57): Show |
60 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.103-3874_103-3872d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492147 | ||||||
chr2:156492223 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.103-3821G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492223 | |||||||
chr2:156492444 | C | CT | 65 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(62): Show |
65 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.103-3585dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156492444 | ||||||
chr2:156492460 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.103-3584C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492460 | |||||||
chr2:156492596 | G | A | 3 | a0002c0002t0011g0050 a0002c0002t0011g0051 a0002c0002t0011g0080 |
3 | HG01496.hp2 HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.103-3448G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492596 | |||||||
chr2:156492748 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.103-3296G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492748 | |||||||
chr2:156492926 | G | C | 1 | a0001c0001t0005g0160 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.103-3118G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156492926 | |||||||
chr2:156493050 | G | A | 1 | a0002c0002t0001g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-2994G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493050 | |||||||
chr2:156493356 | A | G | 1 | a0003c0003t0007g0063 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.103-2688A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493356 | |||||||
chr2:156493425 | C | T | 245 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(242): Show |
245 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.103-2619C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493425 | |||||||
chr2:156493700 | C | T | 1 | a0001c0001t0017g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.103-2344C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493700 | |||||||
chr2:156493706 | C | T | 1 | a0001c0001t0005g0171 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.103-2338C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493706 | |||||||
chr2:156493813 | A | G | 1 | a0002c0002t0006g0117 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.103-2231A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493813 | |||||||
chr2:156493926 | A | ATGTATGT others(3): Show |
2 | a0001c0001t0001g0095 a0001c0001t0001g0102 |
2 | HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.103-2115_103-2114i others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493926 | ||||||
chr2:156493926 | A | ATGTGTGT others(7): Show |
1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.103-2098_103-2085d others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493926 | ||||||
chr2:156493926 | A | ATGTGTGT others(9): Show |
3 | a0002c0002t0002g0161 a0002c0002t0002g0178 a0002c0002t0006g0175 |
3 | HG02109.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.103-2100_103-2085d others(18): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493926 | ||||||
chr2:156493926 | A | ATGTGTGT others(11): Show |
2 | a0002c0002t0002g0176 a0002c0002t0002g0177 |
2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.103-2102_103-2085d others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493926 | ||||||
chr2:156493926 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.103-2118A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493926 | |||||||
chr2:156493926 | ATG | A | 3 | a0002c0002t0001g0173 a0002c0002t0001g0182 a0002c0002t0019g0185 |
3 | HG03098.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.103-2086_103-2085d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493926 | ||||||
chr2:156493958 | G | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0189 others(1): Show |
4 | HG01993.hp2 HG02109.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-2086G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156493958 | |||||||
chr2:156493958 | G | GTA | 76 | a0001c0001t0001g0003 a0001c0001t0001g0062 a0001c0001t0001g0187 others(73): Show |
76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.103-2083_103-2082d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | ||||||
chr2:156493958 | G | GTGTA | 7 | a0001c0001t0001g0198 a0001c0001t0001g0214 a0001c0001t0001g0241 others(4): Show |
7 | HG00741.hp1 HG01517.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | ||||||
chr2:156493958 | G | GTGTGTA | 39 | a0001c0001t0001g0029 a0001c0001t0001g0052 a0001c0001t0001g0077 others(36): Show |
39 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(36): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | ||||||
chr2:156493958 | G | GTGTGTGT others(1): Show |
15 | a0001c0001t0001g0235 a0002c0002t0002g0065 a0002c0002t0002g0084 others(12): Show |
15 | HG00438.hp2 HG00621.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | ||||||
chr2:156493958 | G | GTGTGTGT others(3): Show |
21 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0033 others(18): Show |
21 | HG00558.hp2 HG00639.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | ||||||
chr2:156493958 | G | GTGTGTGT others(5): Show |
45 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0023 others(42): Show |
45 | HG00140.hp1 HG00544.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | ||||||
chr2:156493958 | G | GTGTGTGT others(7): Show |
11 | a0001c0001t0001g0018 a0001c0001t0001g0027 a0001c0001t0001g0060 others(8): Show |
11 | HG00438.hp1 HG00741.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | ||||||
chr2:156493958 | G | GTGTGTGT others(9): Show |
6 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0073 others(3): Show |
6 | HG01243.hp2 HG03654.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-2085_103-2084i others(18): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | ||||||
chr2:156493958 | G | GTGTGTGT others(11): Show |
2 | a0001c0001t0010g0031 a0002c0002t0008g0127 |
2 | HG02071.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.103-2085_103-2084i others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 156493958 | ||||||
chr2:156494024 | A | G | 1 | a0001c0001t0003g0008 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.103-2020A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494024 | |||||||
chr2:156494031 | A | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(73): Show |
76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.103-2013A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494031 | |||||||
chr2:156494204 | T | C | 1 | a0003c0003t0007g0184 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.103-1840T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494204 | |||||||
chr2:156494336 | T | G | 5 | a0001c0001t0003g0037 a0001c0001t0003g0071 a0001c0001t0003g0072 others(2): Show |
5 | HG00639.hp1 HG01884.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-1708T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494336 | |||||||
chr2:156494414 | A | G | 7 | a0001c0001t0001g0062 a0002c0002t0006g0039 a0002c0002t0006g0117 others(4): Show |
7 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-1630A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494414 | |||||||
chr2:156494555 | T | G | 1 | a0002c0002t0004g0025 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.103-1489T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494555 | |||||||
chr2:156494818 | T | A | 152 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(149): Show |
152 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.103-1226T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494818 | |||||||
chr2:156494855 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.103-1189G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156494855 | |||||||
chr2:156495006 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0102 |
3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.103-1038C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156495006 | |||||||
chr2:156495176 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0187 others(73): Show |
76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.103-868C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156495176 | |||||||
chr2:156495312 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.103-732C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156495312 | |||||||
chr2:156495892 | A | G | 1 | a0002c0002t0006g0039 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.103-152A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156495892 | |||||||
chr2:156495906 | A | G | 74 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0187 others(71): Show |
74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.103-138A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 2/16 | chr2 | 156495906 | |||||||
chr2:156496232 | T | A | 1 | a0002c0002t0002g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.274+17T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156496232 | |||||||
chr2:156496234 | T | A | 1 | a0002c0002t0012g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.274+19T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156496234 | |||||||
chr2:156496478 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.274+263G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156496478 | |||||||
chr2:156496669 | C | CTT | 150 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(147): Show |
150 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.274+455_274+456ins others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156496669 | ||||||
chr2:156496669 | CTATATTT others(6): Show |
C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0057 others(75): Show |
78 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.274+456_274+468del others(13): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156496669 | ||||||
chr2:156496786 | A | G | 1 | a0001c0001t0005g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.274+571A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156496786 | |||||||
chr2:156496869 | T | TC | 228 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(225): Show |
228 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.274+655dupC | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156496869 | ||||||
chr2:156496959 | TTCTG | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(70): Show |
73 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.274+748_274+751del others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156496959 | ||||||
chr2:156497169 | T | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.274+954T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156497169 | |||||||
chr2:156497991 | C | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.274+1776C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156497991 | |||||||
chr2:156498046 | A | G | 1 | a0002c0002t0014g0078 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.274+1831A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498046 | |||||||
chr2:156498132 | G | C | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+1917G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498132 | |||||||
chr2:156498279 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.274+2064A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498279 | |||||||
chr2:156498400 | G | C | 6 | a0003c0003t0005g0158 a0003c0003t0007g0163 a0003c0003t0007g0164 others(3): Show |
6 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+2185G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498400 | |||||||
chr2:156498405 | A | T | 5 | a0002c0002t0002g0030 a0002c0002t0002g0079 a0002c0002t0002g0087 others(2): Show |
5 | HG00323.hp2 HG01261.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+2190A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498405 | |||||||
chr2:156498456 | G | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(167): Show |
170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.274+2241G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498456 | |||||||
chr2:156498566 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(176): Show |
179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.274+2351G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156498566 | |||||||
chr2:156499429 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.274+3214G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156499429 | |||||||
chr2:156499648 | T | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(167): Show |
170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.274+3433T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156499648 | |||||||
chr2:156499739 | T | C | 1 | a0002c0002t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.274+3524T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156499739 | |||||||
chr2:156499944 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.274+3729A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156499944 | |||||||
chr2:156499948 | A | C | 175 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.274+3733A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156499948 | |||||||
chr2:156500454 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.274+4239A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156500454 | |||||||
chr2:156500642 | A | G | 1 | a0002c0002t0020g0021 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.274+4427A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156500642 | |||||||
chr2:156500694 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.274+4479C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156500694 | |||||||
chr2:156500779 | T | C | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.274+4564T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156500779 | |||||||
chr2:156501291 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.274+5076T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501291 | |||||||
chr2:156501342 | G | A | 18 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(15): Show |
18 | HG00558.hp1 HG00639.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.274+5127G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501342 | |||||||
chr2:156501540 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.274+5325A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501540 | |||||||
chr2:156501696 | A | T | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.274+5481A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501696 | |||||||
chr2:156501811 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.274+5596G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501811 | |||||||
chr2:156501874 | T | C | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+5659T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156501874 | |||||||
chr2:156502028 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.274+5813G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502028 | |||||||
chr2:156502057 | T | C | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.274+5842T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502057 | |||||||
chr2:156502104 | A | ATG | 5 | a0003c0003t0007g0163 a0003c0003t0007g0164 a0003c0003t0007g0165 others(2): Show |
5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+5909_274+5910d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156502104 | ||||||
chr2:156502104 | ATG | A | 168 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(165): Show |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.274+5909_274+5910d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156502104 | ||||||
chr2:156502111 | T | C | 1 | a0002c0002t0001g0182 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.274+5896T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502111 | |||||||
chr2:156502168 | C | T | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.274+5953C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502168 | |||||||
chr2:156502200 | C | T | 5 | a0003c0003t0007g0163 a0003c0003t0007g0164 a0003c0003t0007g0165 others(2): Show |
5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.274+5985C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502200 | |||||||
chr2:156502237 | T | A | 1 | a0001c0001t0001g0192 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.274+6022T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502237 | |||||||
chr2:156502238 | T | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.274+6023T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502238 | |||||||
chr2:156502245 | T | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.274+6030T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502245 | |||||||
chr2:156502252 | G | A | 2 | a0002c0002t0002g0020 a0002c0002t0002g0089 |
2 | NA18943.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.274+6037G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502252 | |||||||
chr2:156502326 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0105 |
2 | NA19067.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.274+6111G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502326 | |||||||
chr2:156502552 | G | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01993.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.274+6337G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502552 | |||||||
chr2:156502615 | T | C | 6 | a0003c0003t0005g0158 a0003c0003t0007g0163 a0003c0003t0007g0164 others(3): Show |
6 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+6400T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502615 | |||||||
chr2:156502749 | TTGTTA | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0056 a0001c0001t0001g0092 others(10): Show |
13 | HG00140.hp1 HG02074.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.274+6541_274+6545d others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156502749 | ||||||
chr2:156502862 | A | AT | 179 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(176): Show |
179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.274+6655dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156502862 | ||||||
chr2:156502893 | A | T | 6 | a0003c0003t0005g0158 a0003c0003t0007g0163 a0003c0003t0007g0164 others(3): Show |
6 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.274+6678A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502893 | |||||||
chr2:156502963 | T | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.274+6748T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502963 | |||||||
chr2:156502976 | T | C | 7 | a0002c0002t0009g0034 a0002c0002t0009g0118 a0002c0002t0009g0119 others(4): Show |
7 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.274+6761T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156502976 | |||||||
chr2:156503014 | A | T | 86 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(83): Show |
86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.274+6799A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503014 | |||||||
chr2:156503044 | C | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(173): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.274+6829C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503044 | |||||||
chr2:156503125 | T | A | 2 | a0001c0001t0005g0179 a0002c0002t0001g0194 |
2 | HG02071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.274+6910T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503125 | |||||||
chr2:156503168 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.274+6953G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503168 | |||||||
chr2:156503400 | G | A | 2 | a0002c0002t0012g0046 a0002c0002t0012g0074 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.274+7185G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503400 | |||||||
chr2:156503574 | G | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0145 |
2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.275-7222G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503574 | |||||||
chr2:156503643 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.275-7153A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503643 | |||||||
chr2:156503657 | A | G | 4 | a0002c0002t0009g0034 a0002c0002t0009g0118 a0002c0002t0009g0119 others(1): Show |
4 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-7139A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503657 | |||||||
chr2:156503702 | G | C | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-7094G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503702 | |||||||
chr2:156503748 | TAA | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0102 |
3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.275-7045_275-7044d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156503748 | ||||||
chr2:156503764 | G | A | 87 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(84): Show |
87 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.275-7032G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503764 | |||||||
chr2:156503883 | C | T | 4 | a0002c0002t0002g0020 a0002c0002t0002g0089 a0002c0002t0002g0090 others(1): Show |
4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.275-6913C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503883 | |||||||
chr2:156503935 | A | G | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-6861A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156503935 | |||||||
chr2:156504106 | C | G | 1 | a0002c0002t0002g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.275-6690C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504106 | |||||||
chr2:156504122 | A | AATAG | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-6671_275-6670i others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156504122 | ||||||
chr2:156504220 | A | G | 8 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
8 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-6576A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504220 | |||||||
chr2:156504480 | A | T | 1 | a0002c0002t0002g0178 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.275-6316A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504480 | |||||||
chr2:156504590 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-6206G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504590 | |||||||
chr2:156504777 | G | A | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.275-6019G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504777 | |||||||
chr2:156504778 | G | C | 1 | a0002c0002t0020g0021 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.275-6018G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504778 | |||||||
chr2:156504936 | G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.275-5860G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156504936 | |||||||
chr2:156505200 | A | G | 5 | a0001c0001t0001g0107 a0001c0001t0001g0139 a0001c0001t0001g0142 others(2): Show |
5 | NA18747.hp1 NA18999.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-5596A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505200 | |||||||
chr2:156505287 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.275-5509A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505287 | |||||||
chr2:156505628 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.275-5168T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505628 | |||||||
chr2:156505688 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.275-5108T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505688 | |||||||
chr2:156505780 | G | A | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.275-5016G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505780 | |||||||
chr2:156505782 | A | G | 1 | a0002c0002t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.275-5014A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156505782 | |||||||
chr2:156506263 | A | G | 1 | a0002c0002t0002g0138 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.275-4533A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156506263 | |||||||
chr2:156506763 | C | A | 5 | a0003c0003t0007g0163 a0003c0003t0007g0164 a0003c0003t0007g0165 others(2): Show |
5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-4033C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156506763 | |||||||
chr2:156506816 | C | T | 3 | a0001c0001t0001g0196 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG00323.hp1 HG01106.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.275-3980C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156506816 | |||||||
chr2:156507036 | C | T | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.275-3760C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507036 | |||||||
chr2:156507231 | T | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-3565T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507231 | |||||||
chr2:156507326 | CT | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.275-3457delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156507326 | ||||||
chr2:156507427 | A | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0102 |
3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.275-3369A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507427 | |||||||
chr2:156507516 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-3280A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507516 | |||||||
chr2:156507539 | G | C | 3 | a0001c0004t0001g0199 a0001c0004t0001g0218 a0001c0004t0001g0219 |
3 | HG00140.hp2 HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.275-3257G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507539 | |||||||
chr2:156507596 | G | T | 5 | a0001c0001t0001g0195 a0001c0001t0001g0223 a0001c0001t0001g0237 others(2): Show |
5 | HG00544.hp2 NA18950.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-3200G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507596 | |||||||
chr2:156507682 | G | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-3114G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507682 | |||||||
chr2:156507729 | C | A | 1 | a0002c0002t0011g0080 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.275-3067C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507729 | |||||||
chr2:156507876 | C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.275-2920C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156507876 | |||||||
chr2:156508319 | T | G | 1 | a0003c0003t0007g0063 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.275-2477T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156508319 | |||||||
chr2:156508323 | G | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0092 |
2 | HG02602.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.275-2473G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156508323 | |||||||
chr2:156508561 | G | T | 1 | a0002c0002t0011g0050 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.275-2235G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156508561 | |||||||
chr2:156508571 | G | C | 1 | a0002c0002t0004g0028 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.275-2225G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156508571 | |||||||
chr2:156508629 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.275-2167T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156508629 | |||||||
chr2:156509081 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(52): Show |
55 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.275-1715C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509081 | |||||||
chr2:156509200 | T | C | 1 | a0002c0002t0009g0118 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.275-1596T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509200 | |||||||
chr2:156509528 | T | C | 5 | a0003c0003t0007g0163 a0003c0003t0007g0164 a0003c0003t0007g0165 others(2): Show |
5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.275-1268T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509528 | |||||||
chr2:156509531 | G | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
8 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.275-1265G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509531 | |||||||
chr2:156509559 | C | T | 2 | a0001c0001t0005g0166 a0001c0001t0005g0180 |
2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.275-1237C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509559 | |||||||
chr2:156509753 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.275-1043G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509753 | |||||||
chr2:156509765 | C | CTTTT | 5 | a0001c0001t0001g0042 a0001c0001t0001g0106 a0001c0001t0001g0109 others(2): Show |
5 | HG01261.hp2 HG02895.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-1015_275-1012d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156509765 | ||||||
chr2:156509765 | C | CTTTTT | 84 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.275-1016_275-1012d others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156509765 | ||||||
chr2:156509765 | C | CTTTTTT | 74 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0043 others(71): Show |
74 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.275-1017_275-1012d others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156509765 | ||||||
chr2:156509765 | C | CTTTTTTT | 11 | a0001c0001t0001g0222 a0001c0001t0001g0225 a0001c0001t0003g0011 others(8): Show |
11 | HG02258.hp2 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.275-1018_275-1012d others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156509765 | ||||||
chr2:156509784 | T | TTTTTTTA | 7 | a0001c0001t0005g0179 a0002c0002t0001g0194 a0003c0003t0005g0158 others(4): Show |
7 | HG01891.hp2 HG02071.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.275-1012_275-1011i others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509784 | |||||||
chr2:156509804 | C | T | 7 | a0002c0002t0009g0034 a0002c0002t0009g0118 a0002c0002t0009g0119 others(4): Show |
7 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.275-992C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509804 | |||||||
chr2:156509834 | C | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.275-962C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509834 | |||||||
chr2:156509885 | G | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.275-911G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509885 | |||||||
chr2:156509898 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0100 a0001c0001t0015g0098 |
3 | HG02056.hp1 NA19004.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.275-898C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156509898 | |||||||
chr2:156510218 | C | CTCTT | 5 | a0002c0002t0002g0030 a0002c0002t0002g0079 a0002c0002t0002g0087 others(2): Show |
5 | HG00323.hp2 HG01261.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.275-565_275-562dup others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 156510218 | ||||||
chr2:156510259 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.275-537C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156510259 | |||||||
chr2:156510377 | G | A | 1 | a0002c0002t0002g0084 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.275-419G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156510377 | |||||||
chr2:156510518 | A | G | 1 | a0002c0002t0020g0021 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.275-278A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156510518 | |||||||
chr2:156510590 | C | T | 1 | a0001c0001t0010g0031 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.275-206C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156510590 | |||||||
chr2:156510599 | C | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG00639.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.275-197C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 3/16 | chr2 | 156510599 | |||||||
chr2:156510987 | G | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+67G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 4/16 | chr2 | 156510987 | |||||||
chr2:156511741 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.400-479G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 4/16 | chr2 | 156511741 | |||||||
chr2:156511906 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.400-314A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 4/16 | chr2 | 156511906 | |||||||
chr2:156512365 | T | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.497+48T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 5/16 | chr2 | 156512365 | |||||||
chr2:156512649 | G | T | 3 | a0001c0001t0001g0196 a0001c0001t0001g0212 a0001c0001t0001g0213 |
3 | HG00323.hp1 HG01106.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.497+332G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 5/16 | chr2 | 156512649 | |||||||
chr2:156512710 | G | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.497+393G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 5/16 | chr2 | 156512710 | |||||||
chr2:156512728 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.497+411C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 5/16 | chr2 | 156512728 | |||||||
chr2:156512739 | TA | T | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.497+424delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 156512739 | ||||||
chr2:156513505 | TG | T | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+10delG | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513505 | |||||||
chr2:156513506 | GT | G | 6 | a0001c0001t0003g0037 a0001c0001t0003g0071 a0001c0001t0003g0072 others(3): Show |
6 | HG00639.hp1 HG01884.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+24delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156513506 | ||||||
chr2:156513514 | T | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+18T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513514 | |||||||
chr2:156513585 | A | C | 3 | a0001c0001t0001g0058 a0001c0001t0001g0145 a0001c0001t0017g0135 |
3 | HG02683.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.661+89A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513585 | |||||||
chr2:156513654 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.661+158G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513654 | |||||||
chr2:156513683 | A | G | 1 | a0003c0003t0007g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.661+187A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156513683 | |||||||
chr2:156514129 | C | CT | 5 | a0003c0003t0007g0163 a0003c0003t0007g0164 a0003c0003t0007g0165 others(2): Show |
5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+648dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156514129 | ||||||
chr2:156514129 | CT | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0043 others(88): Show |
91 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.661+648delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156514129 | ||||||
chr2:156514129 | CTT | C | 87 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(84): Show |
87 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.661+647_661+648del others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156514129 | ||||||
chr2:156514493 | T | C | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+997T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156514493 | |||||||
chr2:156514595 | A | G | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.661+1099A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156514595 | |||||||
chr2:156514713 | T | C | 247 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.661+1217T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156514713 | |||||||
chr2:156514737 | A | G | 1 | a0002c0002t0001g0182 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.661+1241A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156514737 | |||||||
chr2:156515221 | C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.661+1725C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156515221 | |||||||
chr2:156515345 | C | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(78): Show |
81 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.661+1849C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156515345 | |||||||
chr2:156515488 | ATTG | A | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+1997_661+1999d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156515488 | ||||||
chr2:156515620 | T | A | 1 | a0001c0001t0001g0145 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.661+2124T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156515620 | |||||||
chr2:156515922 | A | G | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+2426A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156515922 | |||||||
chr2:156516001 | T | C | 1 | a0002c0002t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.661+2505T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156516001 | |||||||
chr2:156516125 | T | C | 1 | a0002c0002t0002g0053 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.661+2629T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156516125 | |||||||
chr2:156516411 | C | T | 1 | a0002c0002t0008g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.661+2915C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156516411 | |||||||
chr2:156516504 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0225 |
2 | NA19004.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.661+3008T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156516504 | |||||||
chr2:156516595 | A | G | 1 | a0001c0001t0013g0069 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.661+3099A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156516595 | |||||||
chr2:156516813 | CACTT | C | 5 | a0003c0003t0007g0163 a0003c0003t0007g0164 a0003c0003t0007g0165 others(2): Show |
5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+3322_661+3325d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156516813 | ||||||
chr2:156517100 | G | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+3604G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517100 | |||||||
chr2:156517345 | A | G | 2 | a0003c0003t0007g0012 a0003c0003t0007g0063 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.661+3849A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517345 | |||||||
chr2:156517358 | C | T | 2 | a0001c0001t0005g0179 a0002c0002t0001g0194 |
2 | HG02071.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.661+3862C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517358 | |||||||
chr2:156517497 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+4001T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517497 | |||||||
chr2:156517780 | A | G | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+4284A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517780 | |||||||
chr2:156517895 | G | A | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+4399G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156517895 | |||||||
chr2:156518004 | A | G | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.661+4508A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156518004 | |||||||
chr2:156518480 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.661+4984T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156518480 | |||||||
chr2:156518490 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+4994G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156518490 | |||||||
chr2:156518670 | T | C | 2 | a0001c0001t0005g0055 a0002c0002t0012g0075 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.661+5174T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156518670 | |||||||
chr2:156519210 | T | G | 4 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+5714T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519210 | |||||||
chr2:156519211 | G | T | 85 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(82): Show |
85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.661+5715G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519211 | |||||||
chr2:156519305 | A | T | 7 | a0002c0002t0002g0013 a0002c0002t0002g0048 a0002c0002t0002g0053 others(4): Show |
7 | HG02129.hp1 HG03654.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+5809A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519305 | |||||||
chr2:156519444 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.661+5948A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519444 | |||||||
chr2:156519453 | A | T | 1 | a0001c0001t0001g0022 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.661+5957A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519453 | |||||||
chr2:156519658 | T | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+6162T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519658 | |||||||
chr2:156519659 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.661+6163G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519659 | |||||||
chr2:156519663 | C | G | 2 | a0002c0002t0012g0046 a0002c0002t0012g0074 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.661+6167C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519663 | |||||||
chr2:156519707 | C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.661+6211C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519707 | |||||||
chr2:156519725 | G | A | 2 | a0002c0002t0012g0046 a0002c0002t0012g0074 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.661+6229G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519725 | |||||||
chr2:156519779 | C | T | 3 | a0002c0002t0002g0149 a0002c0002t0002g0150 a0002c0002t0002g0151 |
3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.661+6283C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519779 | |||||||
chr2:156519960 | G | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(173): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.661+6464G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519960 | |||||||
chr2:156519961 | G | A | 1 | a0001c0001t0016g0049 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.661+6465G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156519961 | |||||||
chr2:156520207 | G | T | 1 | a0002c0002t0011g0050 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.661+6711G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156520207 | |||||||
chr2:156520270 | A | G | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.661+6774A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156520270 | |||||||
chr2:156520355 | CA | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+6861delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156520355 | ||||||
chr2:156520433 | A | G | 1 | a0001c0001t0005g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661+6937A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156520433 | |||||||
chr2:156520560 | G | GTTATTTA others(1): Show |
2 | a0002c0002t0001g0181 a0002c0002t0001g0183 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+7099_661+7106d others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156520560 | ||||||
chr2:156520560 | GTTAT | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0103 others(82): Show |
85 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.661+7103_661+7106d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156520560 | ||||||
chr2:156520560 | GTTATTTA others(1): Show |
G | 143 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(140): Show |
143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.661+7099_661+7106d others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156520560 | ||||||
chr2:156520560 | GTTATTTA others(5): Show |
G | 2 | a0001c0001t0003g0205 a0001c0001t0005g0160 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.661+7095_661+7106d others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156520560 | ||||||
chr2:156520828 | C | T | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.661+7332C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156520828 | |||||||
chr2:156520990 | A | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+7494A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156520990 | |||||||
chr2:156521444 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.661+7948A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156521444 | |||||||
chr2:156521687 | A | G | 8 | a0001c0001t0005g0179 a0002c0002t0001g0194 a0003c0003t0005g0158 others(5): Show |
8 | HG01891.hp2 HG02071.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.661+8191A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156521687 | |||||||
chr2:156521830 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.661+8334A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156521830 | |||||||
chr2:156521957 | C | T | 5 | a0001c0001t0001g0195 a0001c0001t0001g0223 a0001c0001t0001g0237 others(2): Show |
5 | HG00544.hp2 NA18950.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+8461C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156521957 | |||||||
chr2:156522021 | A | G | 167 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.661+8525A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522021 | |||||||
chr2:156522105 | G | A | 1 | a0002c0002t0004g0083 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.661+8609G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522105 | |||||||
chr2:156522107 | A | G | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.661+8611A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522107 | |||||||
chr2:156522311 | C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.661+8815C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522311 | |||||||
chr2:156522332 | T | C | 1 | a0002c0002t0019g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.661+8836T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522332 | |||||||
chr2:156522444 | C | T | 2 | a0002c0002t0002g0085 a0002c0002t0021g0054 |
2 | HG01106.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.661+8948C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522444 | |||||||
chr2:156522528 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0109 |
2 | NA19060.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.661+9032A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522528 | |||||||
chr2:156522683 | CT | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.661+9202delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156522683 | ||||||
chr2:156522921 | T | A | 4 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+9425T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156522921 | |||||||
chr2:156522948 | AT | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(78): Show |
81 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.661+9456delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156522948 | ||||||
chr2:156523248 | C | T | 1 | a0001c0001t0005g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661+9752C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523248 | |||||||
chr2:156523291 | T | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+9795T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523291 | |||||||
chr2:156523331 | G | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+9835G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523331 | |||||||
chr2:156523500 | C | T | 1 | a0002c0002t0009g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.661+10004C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523500 | |||||||
chr2:156523649 | T | C | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+10153T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523649 | |||||||
chr2:156523670 | C | CTAGA | 76 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0027 others(73): Show |
76 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.661+10221_661+1022 others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | ||||||
chr2:156523670 | C | CTAGATAG others(1): Show |
21 | a0001c0001t0001g0109 a0001c0001t0001g0116 a0001c0001t0001g0136 others(18): Show |
21 | HG01346.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.661+10217_661+1022 others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | ||||||
chr2:156523670 | C | CTAGATAG others(5): Show |
3 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0003g0037 |
3 | HG02683.hp1 HG04199.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.661+10213_661+1022 others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | ||||||
chr2:156523670 | CTAGA | C | 31 | a0001c0001t0001g0026 a0001c0001t0001g0062 a0001c0001t0001g0096 others(28): Show |
31 | HG00323.hp2 HG00558.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.661+10221_661+1022 others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | ||||||
chr2:156523670 | CTAGATAG others(1): Show |
C | 7 | a0001c0001t0001g0216 a0001c0001t0001g0222 a0001c0001t0001g0225 others(4): Show |
7 | HG01123.hp1 HG02451.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+10217_661+1022 others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | ||||||
chr2:156523670 | CTAGATAG others(5): Show |
C | 5 | a0001c0001t0001g0056 a0001c0001t0005g0172 a0002c0002t0002g0087 others(2): Show |
5 | HG01884.hp2 HG01928.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+10213_661+1022 others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | ||||||
chr2:156523670 | CTAGATAG others(9): Show |
C | 2 | a0002c0002t0012g0046 a0002c0002t0012g0075 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.661+10209_661+1022 others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156523670 | ||||||
chr2:156523804 | G | A | 5 | a0001c0001t0003g0037 a0001c0001t0003g0071 a0001c0001t0003g0072 others(2): Show |
5 | HG00639.hp1 HG01884.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+10308G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156523804 | |||||||
chr2:156524040 | A | G | 2 | a0002c0002t0001g0181 a0002c0002t0001g0183 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+10544A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156524040 | |||||||
chr2:156524067 | G | A | 170 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(167): Show |
170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.661+10571G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156524067 | |||||||
chr2:156524560 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.661+11064T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156524560 | |||||||
chr2:156525242 | A | G | 49 | a0002c0002t0002g0013 a0002c0002t0002g0020 a0002c0002t0002g0030 others(46): Show |
49 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.661+11746A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525242 | |||||||
chr2:156525365 | G | C | 1 | a0001c0001t0005g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.661+11869G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525365 | |||||||
chr2:156525567 | A | T | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+12071A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525567 | |||||||
chr2:156525628 | A | C | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+12132A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525628 | |||||||
chr2:156525659 | T | C | 1 | a0002c0002t0001g0182 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.661+12163T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525659 | |||||||
chr2:156525807 | T | G | 4 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.661+12311T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156525807 | |||||||
chr2:156526109 | G | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+12613G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156526109 | |||||||
chr2:156526296 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.661+12800C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156526296 | |||||||
chr2:156526307 | C | A | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.661+12811C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156526307 | |||||||
chr2:156526601 | T | TAGTTTA | 247 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.661+13108_661+1311 others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156526601 | ||||||
chr2:156526750 | T | C | 1 | a0002c0002t0002g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.661+13254T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156526750 | |||||||
chr2:156527106 | C | G | 6 | a0003c0003t0005g0158 a0003c0003t0007g0163 a0003c0003t0007g0164 others(3): Show |
6 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+13610C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527106 | |||||||
chr2:156527163 | C | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+13667C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527163 | |||||||
chr2:156527433 | C | G | 85 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(82): Show |
85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.661+13937C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527433 | |||||||
chr2:156527456 | C | T | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+13960C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527456 | |||||||
chr2:156527706 | G | A | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+14210G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527706 | |||||||
chr2:156527724 | T | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+14228T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527724 | |||||||
chr2:156527849 | G | A | 1 | a0001c0001t0005g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.661+14353G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156527849 | |||||||
chr2:156528239 | C | T | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+14743C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528239 | |||||||
chr2:156528536 | C | G | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+15040C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528536 | |||||||
chr2:156528587 | C | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+15091C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528587 | |||||||
chr2:156528594 | C | G | 1 | a0003c0003t0007g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.661+15098C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528594 | |||||||
chr2:156528633 | C | T | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+15137C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528633 | |||||||
chr2:156528773 | A | AT | 3 | a0002c0002t0002g0149 a0002c0002t0002g0150 a0002c0002t0002g0151 |
3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.661+15283dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156528773 | ||||||
chr2:156528887 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0096 a0001c0001t0001g0186 |
3 | NA18959.hp2 NA19000.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.661+15391C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528887 | |||||||
chr2:156528900 | G | C | 1 | a0001c0001t0016g0049 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.661+15404G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528900 | |||||||
chr2:156528971 | A | T | 1 | a0002c0002t0009g0118 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.661+15475A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156528971 | |||||||
chr2:156529062 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.661+15566A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529062 | |||||||
chr2:156529085 | G | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.661+15589G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529085 | |||||||
chr2:156529093 | G | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(173): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.661+15597G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529093 | |||||||
chr2:156529103 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0113 |
2 | HG01243.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.661+15607T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529103 | |||||||
chr2:156529105 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.661+15609T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529105 | |||||||
chr2:156529134 | C | T | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.661+15638C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529134 | |||||||
chr2:156529210 | A | G | 1 | a0002c0002t0002g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.661+15714A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529210 | |||||||
chr2:156529212 | G | GT | 177 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.661+15722dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156529212 | ||||||
chr2:156529265 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.661+15769G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529265 | |||||||
chr2:156529318 | A | G | 2 | a0003c0003t0007g0012 a0003c0003t0007g0063 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.661+15822A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529318 | |||||||
chr2:156529582 | T | G | 7 | a0002c0002t0006g0039 a0002c0002t0006g0117 a0002c0002t0006g0154 others(4): Show |
7 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.661+16086T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529582 | |||||||
chr2:156529620 | C | G | 5 | a0001c0001t0003g0037 a0001c0001t0003g0071 a0001c0001t0003g0072 others(2): Show |
5 | HG00639.hp1 HG01884.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+16124C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529620 | |||||||
chr2:156529798 | A | C | 2 | a0002c0002t0002g0085 a0002c0002t0021g0054 |
2 | HG01106.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.661+16302A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529798 | |||||||
chr2:156529810 | G | A | 1 | a0001c0001t0005g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.661+16314G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529810 | |||||||
chr2:156529833 | T | G | 3 | a0002c0002t0002g0149 a0002c0002t0002g0150 a0002c0002t0002g0151 |
3 | HG01884.hp2 HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.661+16337T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529833 | |||||||
chr2:156529870 | C | T | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+16374C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529870 | |||||||
chr2:156529915 | G | A | 1 | a0002c0002t0012g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.661+16419G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529915 | |||||||
chr2:156529938 | A | G | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+16442A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529938 | |||||||
chr2:156529981 | G | C | 5 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+16485G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529981 | |||||||
chr2:156529989 | G | A | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+16493G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156529989 | |||||||
chr2:156530038 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.661+16542C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530038 | |||||||
chr2:156530047 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.661+16551T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530047 | |||||||
chr2:156530292 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.661+16796A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530292 | |||||||
chr2:156530302 | T | TTTGCTGA others(2): Show |
183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+16811_661+1681 others(13): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156530302 | ||||||
chr2:156530359 | G | C | 1 | a0002c0002t0019g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.661+16863G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530359 | |||||||
chr2:156530465 | A | G | 2 | a0002c0002t0002g0085 a0002c0002t0021g0054 |
2 | HG01106.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.661+16969A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530465 | |||||||
chr2:156530574 | G | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.661+17078G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530574 | |||||||
chr2:156530642 | C | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+17146C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530642 | |||||||
chr2:156530674 | A | C | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.661+17178A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530674 | |||||||
chr2:156530736 | T | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(173): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.661+17240T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156530736 | |||||||
chr2:156531111 | C | T | 1 | a0002c0002t0002g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.661+17615C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531111 | |||||||
chr2:156531114 | T | G | 3 | a0002c0002t0004g0121 a0002c0002t0004g0140 a0002c0002t0004g0141 |
3 | NA18952.hp2 NA18999.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.661+17618T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531114 | |||||||
chr2:156531136 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.661+17640A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531136 | |||||||
chr2:156531148 | T | G | 1 | a0002c0002t0002g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.661+17652T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531148 | |||||||
chr2:156531207 | T | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.661+17711T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531207 | |||||||
chr2:156531551 | C | T | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.661+18055C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531551 | |||||||
chr2:156531704 | T | A | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.662-17904T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531704 | |||||||
chr2:156531856 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.662-17752G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531856 | |||||||
chr2:156531868 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.662-17740G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156531868 | |||||||
chr2:156532013 | CT | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.662-17589delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156532013 | ||||||
chr2:156532058 | A | C | 1 | a0002c0002t0004g0083 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.662-17550A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532058 | |||||||
chr2:156532122 | C | T | 1 | a0003c0003t0007g0165 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.662-17486C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532122 | |||||||
chr2:156532138 | T | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-17470T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532138 | |||||||
chr2:156532190 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.662-17418A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532190 | |||||||
chr2:156532236 | G | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.662-17372G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532236 | |||||||
chr2:156532270 | G | A | 4 | a0002c0002t0002g0020 a0002c0002t0002g0089 a0002c0002t0002g0090 others(1): Show |
4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-17338G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532270 | |||||||
chr2:156532475 | A | T | 28 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0003g0001 others(25): Show |
28 | HG00558.hp1 HG00639.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.662-17133A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532475 | |||||||
chr2:156532515 | A | G | 3 | a0002c0002t0011g0050 a0002c0002t0011g0051 a0002c0002t0011g0080 |
3 | HG01496.hp2 HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.662-17093A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532515 | |||||||
chr2:156532682 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02735.hp2 HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.662-16926C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532682 | |||||||
chr2:156532699 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-16909G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532699 | |||||||
chr2:156532763 | T | C | 1 | a0002c0002t0006g0117 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.662-16845T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532763 | |||||||
chr2:156532949 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-16659T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532949 | |||||||
chr2:156532978 | G | T | 1 | a0002c0002t0002g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.662-16630G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156532978 | |||||||
chr2:156533505 | A | C | 1 | a0001c0004t0001g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.662-16103A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533505 | |||||||
chr2:156533514 | T | A | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-16094T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533514 | |||||||
chr2:156533532 | G | GT | 7 | a0001c0001t0005g0055 a0001c0001t0005g0160 a0001c0001t0005g0166 others(4): Show |
7 | HG02622.hp2 HG02717.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-16070dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156533532 | ||||||
chr2:156533538 | T | A | 1 | a0001c0001t0001g0003 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.662-16070T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533538 | |||||||
chr2:156533599 | C | T | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-16009C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533599 | |||||||
chr2:156533790 | C | G | 5 | a0003c0003t0007g0163 a0003c0003t0007g0164 a0003c0003t0007g0165 others(2): Show |
5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-15818C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533790 | |||||||
chr2:156533905 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-15703G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533905 | |||||||
chr2:156533940 | T | C | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.662-15668T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156533940 | |||||||
chr2:156534111 | A | G | 6 | a0003c0003t0005g0158 a0003c0003t0007g0163 a0003c0003t0007g0164 others(3): Show |
6 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.662-15497A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156534111 | |||||||
chr2:156534226 | T | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-15382T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156534226 | |||||||
chr2:156534251 | C | CCTT | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-15355_662-1535 others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156534251 | ||||||
chr2:156534428 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.662-15180T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156534428 | |||||||
chr2:156534670 | A | G | 5 | a0003c0003t0007g0163 a0003c0003t0007g0164 a0003c0003t0007g0165 others(2): Show |
5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-14938A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156534670 | |||||||
chr2:156534672 | A | G | 2 | a0002c0002t0001g0173 a0002c0002t0005g0159 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.662-14936A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156534672 | |||||||
chr2:156534810 | T | TA | 6 | a0001c0001t0001g0229 a0002c0002t0001g0173 a0002c0002t0001g0182 others(3): Show |
6 | HG00673.hp2 HG02630.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.662-14785dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156534810 | ||||||
chr2:156535064 | G | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(51): Show |
54 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.662-14544G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535064 | |||||||
chr2:156535118 | G | T | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.662-14490G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535118 | |||||||
chr2:156535222 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.662-14386T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535222 | |||||||
chr2:156535274 | TGAGA | T | 7 | a0002c0002t0001g0194 a0002c0002t0002g0020 a0002c0002t0002g0082 others(4): Show |
7 | HG02040.hp1 HG02071.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-14321_662-1431 others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535274 | ||||||
chr2:156535324 | AAG | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(51): Show |
54 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.662-14270_662-1426 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535324 | ||||||
chr2:156535363 | G | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.662-14245G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535363 | |||||||
chr2:156535389 | TG | T | 160 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(157): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.662-14210delG | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535389 | ||||||
chr2:156535394 | G | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.662-14214G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535394 | |||||||
chr2:156535437 | G | GGAGA | 7 | a0002c0002t0008g0162 a0003c0003t0005g0158 a0003c0003t0007g0163 others(4): Show |
7 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.662-14150_662-1414 others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535437 | ||||||
chr2:156535437 | G | GGGGA | 167 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.662-14170_662-1416 others(8): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535437 | ||||||
chr2:156535437 | GGAGAGAG others(3): Show |
G | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.662-14156_662-1414 others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156535437 | ||||||
chr2:156535439 | A | G | 1 | a0001c0001t0003g0002 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.662-14169A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535439 | |||||||
chr2:156535449 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.662-14159A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535449 | |||||||
chr2:156535462 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.662-14146A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535462 | |||||||
chr2:156535520 | T | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.662-14088T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535520 | |||||||
chr2:156535546 | A | G | 1 | a0001c0001t0005g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.662-14062A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156535546 | |||||||
chr2:156536051 | G | A | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0241 others(1): Show |
4 | HG01993.hp2 NA19006.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-13557G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536051 | |||||||
chr2:156536112 | C | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(51): Show |
54 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.662-13496C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536112 | |||||||
chr2:156536196 | G | A | 1 | a0001c0001t0015g0098 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.662-13412G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536196 | |||||||
chr2:156536494 | G | A | 1 | a0002c0002t0008g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.662-13114G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536494 | |||||||
chr2:156536508 | A | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-13100A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536508 | |||||||
chr2:156536587 | C | A | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.662-13021C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536587 | |||||||
chr2:156536652 | C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.662-12956C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536652 | |||||||
chr2:156536762 | C | A | 26 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(23): Show |
26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.662-12846C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536762 | |||||||
chr2:156536775 | C | G | 1 | a0002c0002t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662-12833C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536775 | |||||||
chr2:156536835 | A | G | 4 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 others(1): Show |
4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-12773A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536835 | |||||||
chr2:156536916 | A | G | 4 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 others(1): Show |
4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-12692A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156536916 | |||||||
chr2:156537062 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.662-12546A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537062 | |||||||
chr2:156537092 | T | C | 1 | a0002c0002t0002g0084 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.662-12516T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537092 | |||||||
chr2:156537225 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.662-12383C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537225 | |||||||
chr2:156537237 | T | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.662-12371T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537237 | |||||||
chr2:156537264 | C | T | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.662-12344C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537264 | |||||||
chr2:156537414 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.662-12194C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537414 | |||||||
chr2:156537549 | G | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.662-12059G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537549 | |||||||
chr2:156537682 | A | C | 4 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 others(1): Show |
4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-11926A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537682 | |||||||
chr2:156537688 | A | G | 4 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 others(1): Show |
4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-11920A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537688 | |||||||
chr2:156537699 | C | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
8 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.662-11909C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537699 | |||||||
chr2:156537886 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0102 |
3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.662-11722G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537886 | |||||||
chr2:156537931 | G | T | 49 | a0002c0002t0002g0013 a0002c0002t0002g0020 a0002c0002t0002g0030 others(46): Show |
49 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.662-11677G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156537931 | |||||||
chr2:156538013 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-11595G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538013 | |||||||
chr2:156538016 | A | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-11592A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538016 | |||||||
chr2:156538243 | C | T | 1 | a0002c0002t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662-11365C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538243 | |||||||
chr2:156538379 | A | G | 1 | a0001c0001t0005g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.662-11229A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538379 | |||||||
chr2:156538437 | A | G | 1 | a0002c0002t0002g0084 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.662-11171A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538437 | |||||||
chr2:156538477 | TA | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(58): Show |
61 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.662-11116delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156538477 | ||||||
chr2:156538554 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.662-11054T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538554 | |||||||
chr2:156538625 | C | A | 1 | a0001c0001t0005g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.662-10983C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538625 | |||||||
chr2:156538631 | T | C | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.662-10977T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538631 | |||||||
chr2:156538760 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.662-10848G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538760 | |||||||
chr2:156538820 | C | CA | 205 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(202): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.662-10770dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156538820 | ||||||
chr2:156538820 | C | CAA | 34 | a0001c0001t0001g0026 a0001c0001t0001g0104 a0001c0001t0001g0109 others(31): Show |
34 | HG00558.hp1 HG00639.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.662-10771_662-1077 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156538820 | ||||||
chr2:156538835 | A | AT | 3 | a0002c0002t0002g0020 a0002c0002t0002g0089 a0002c0002t0002g0091 |
3 | NA18943.hp2 NA18975.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.662-10773_662-1077 others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538835 | |||||||
chr2:156538835 | A | T | 1 | a0002c0002t0002g0090 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.662-10773A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156538835 | |||||||
chr2:156539192 | T | C | 1 | a0002c0002t0002g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.662-10416T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156539192 | |||||||
chr2:156539441 | A | G | 1 | a0002c0002t0002g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.662-10167A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156539441 | |||||||
chr2:156539856 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-9752G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156539856 | |||||||
chr2:156539949 | C | CT | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-9657dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156539949 | ||||||
chr2:156540085 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0100 |
2 | NA19004.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.662-9523A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540085 | |||||||
chr2:156540123 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.662-9485A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540123 | |||||||
chr2:156540349 | C | T | 4 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 others(1): Show |
4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-9259C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540349 | |||||||
chr2:156540596 | C | T | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.662-9012C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540596 | |||||||
chr2:156540605 | A | G | 5 | a0003c0003t0007g0163 a0003c0003t0007g0164 a0003c0003t0007g0165 others(2): Show |
5 | HG02886.hp2 HG02897.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-9003A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540605 | |||||||
chr2:156540642 | G | A | 4 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-8966G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540642 | |||||||
chr2:156540739 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.662-8869A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540739 | |||||||
chr2:156540796 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0105 |
2 | NA19067.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.662-8812G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540796 | |||||||
chr2:156540833 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.662-8775A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540833 | |||||||
chr2:156540981 | C | T | 1 | a0002c0002t0012g0074 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.662-8627C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156540981 | |||||||
chr2:156541327 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(175): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.662-8281A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156541327 | |||||||
chr2:156541820 | G | GTTT | 3 | a0001c0001t0001g0223 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | HG00544.hp2 NA18953.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.662-7787_662-7785d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541820 | ||||||
chr2:156541824 | G | GT | 54 | a0002c0002t0002g0013 a0002c0002t0002g0030 a0002c0002t0002g0048 others(51): Show |
54 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.662-7762dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541824 | ||||||
chr2:156541824 | G | GTT | 18 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 others(15): Show |
18 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.662-7763_662-7762d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541824 | ||||||
chr2:156541824 | G | GTTT | 78 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0042 others(75): Show |
78 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.662-7764_662-7762d others(5): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541824 | ||||||
chr2:156541824 | G | GTTTT | 75 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(72): Show |
75 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.662-7765_662-7762d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541824 | ||||||
chr2:156541824 | G | GTTTTT | 16 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0043 others(13): Show |
16 | HG01192.hp1 HG02071.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.662-7766_662-7762d others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541824 | ||||||
chr2:156541824 | G | T | 5 | a0001c0001t0001g0195 a0001c0001t0001g0223 a0001c0001t0001g0237 others(2): Show |
5 | HG00544.hp2 NA18950.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-7784G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156541824 | |||||||
chr2:156541981 | TG | T | 172 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.662-7625delG | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156541981 | ||||||
chr2:156542171 | C | T | 1 | a0002c0002t0002g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.662-7437C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542171 | |||||||
chr2:156542307 | A | G | 2 | a0001c0001t0010g0019 a0001c0001t0010g0128 |
2 | HG00438.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.662-7301A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542307 | |||||||
chr2:156542335 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.662-7273G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542335 | |||||||
chr2:156542449 | A | C | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.662-7159A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542449 | |||||||
chr2:156542521 | C | T | 5 | a0001c0001t0001g0195 a0001c0001t0001g0223 a0001c0001t0001g0237 others(2): Show |
5 | HG00544.hp2 NA18950.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-7087C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542521 | |||||||
chr2:156542824 | G | A | 1 | a0002c0002t0006g0039 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.662-6784G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542824 | |||||||
chr2:156542879 | T | C | 1 | a0002c0002t0006g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.662-6729T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156542879 | |||||||
chr2:156543038 | C | T | 84 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.662-6570C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543038 | |||||||
chr2:156543100 | A | G | 2 | a0001c0001t0005g0160 a0001c0001t0005g0171 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.662-6508A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543100 | |||||||
chr2:156543206 | C | G | 4 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-6402C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543206 | |||||||
chr2:156543442 | A | C | 1 | a0001c0001t0005g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.662-6166A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543442 | |||||||
chr2:156543784 | C | T | 1 | a0002c0002t0002g0152 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.662-5824C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543784 | |||||||
chr2:156543788 | T | C | 1 | a0002c0002t0006g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.662-5820T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543788 | |||||||
chr2:156543855 | C | T | 1 | a0002c0002t0004g0121 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.662-5753C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156543855 | |||||||
chr2:156544128 | G | A | 1 | a0002c0002t0004g0083 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.662-5480G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544128 | |||||||
chr2:156544188 | G | C | 4 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 others(1): Show |
4 | HG02630.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-5420G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544188 | |||||||
chr2:156544316 | A | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.662-5292A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544316 | |||||||
chr2:156544370 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.662-5238C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544370 | |||||||
chr2:156544376 | G | A | 42 | a0002c0002t0002g0013 a0002c0002t0002g0020 a0002c0002t0002g0030 others(39): Show |
42 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.662-5232G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544376 | |||||||
chr2:156544457 | A | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.662-5151A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544457 | |||||||
chr2:156544593 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.662-5015A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544593 | |||||||
chr2:156544658 | T | C | 4 | a0002c0002t0002g0020 a0002c0002t0002g0089 a0002c0002t0002g0090 others(1): Show |
4 | HG02040.hp1 NA18943.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.662-4950T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544658 | |||||||
chr2:156544757 | A | G | 180 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.662-4851A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544757 | |||||||
chr2:156544894 | T | C | 1 | a0002c0002t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.662-4714T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156544894 | |||||||
chr2:156545042 | A | T | 1 | a0002c0002t0002g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.662-4566A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156545042 | |||||||
chr2:156545114 | A | G | 1 | a0001c0001t0005g0172 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.662-4494A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156545114 | |||||||
chr2:156545342 | C | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.662-4266C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156545342 | |||||||
chr2:156546301 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.662-3307G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156546301 | |||||||
chr2:156546618 | G | A | 86 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(83): Show |
86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.662-2990G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156546618 | |||||||
chr2:156546722 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.662-2886C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156546722 | |||||||
chr2:156546920 | C | CTGTT | 249 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(246): Show |
249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.662-2686_662-2683d others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 156546920 | ||||||
chr2:156547084 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(52): Show |
55 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.662-2524C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547084 | |||||||
chr2:156547125 | G | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(173): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.662-2483G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547125 | |||||||
chr2:156547248 | C | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.662-2360C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547248 | |||||||
chr2:156547399 | A | G | 1 | a0001c0001t0015g0098 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.662-2209A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547399 | |||||||
chr2:156547682 | A | T | 5 | a0001c0001t0005g0160 a0001c0001t0005g0166 a0001c0001t0005g0171 others(2): Show |
5 | HG02622.hp2 HG02717.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.662-1926A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547682 | |||||||
chr2:156547777 | A | G | 1 | a0002c0002t0009g0119 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.662-1831A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156547777 | |||||||
chr2:156548062 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0096 |
2 | NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.662-1546A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548062 | |||||||
chr2:156548201 | G | A | 26 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(23): Show |
26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.662-1407G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548201 | |||||||
chr2:156548309 | C | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.662-1299C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548309 | |||||||
chr2:156548310 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.662-1298C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548310 | |||||||
chr2:156548456 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(53): Show |
56 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.662-1152G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548456 | |||||||
chr2:156548594 | A | G | 1 | a0001c0001t0017g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.662-1014A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548594 | |||||||
chr2:156548909 | C | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.662-699C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156548909 | |||||||
chr2:156549048 | A | G | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.662-560A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156549048 | |||||||
chr2:156549074 | G | A | 1 | a0002c0002t0002g0020 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.662-534G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156549074 | |||||||
chr2:156549451 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.662-157G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 6/16 | chr2 | 156549451 | |||||||
chr2:156549784 | A | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(182): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.826+12A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/16 | chr2 | 156549784 | |||||||
chr2:156549821 | T | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG00639.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+49T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/16 | chr2 | 156549821 | |||||||
chr2:156549956 | A | G | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.826+184A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/16 | chr2 | 156549956 | |||||||
chr2:156550113 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.826+341A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/16 | chr2 | 156550113 | |||||||
chr2:156550246 | T | C | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.827-356T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 7/16 | chr2 | 156550246 | |||||||
chr2:156551111 | A | T | 47 | a0002c0002t0002g0013 a0002c0002t0002g0020 a0002c0002t0002g0030 others(44): Show |
47 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.971+365A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551111 | |||||||
chr2:156551127 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.971+381C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551127 | |||||||
chr2:156551186 | C | A | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.971+440C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551186 | |||||||
chr2:156551208 | AT | A | 172 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(169): Show |
172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.971+463delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551208 | |||||||
chr2:156551265 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.971+519G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551265 | |||||||
chr2:156551353 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.971+607G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551353 | |||||||
chr2:156551355 | C | G | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+609C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551355 | |||||||
chr2:156551539 | A | T | 1 | a0001c0001t0005g0171 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.971+793A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551539 | |||||||
chr2:156551611 | G | A | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+865G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156551611 | |||||||
chr2:156552272 | T | C | 1 | a0002c0002t0001g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.971+1526T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552272 | |||||||
chr2:156552319 | G | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.971+1573G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552319 | |||||||
chr2:156552784 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.971+2038G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552784 | |||||||
chr2:156552822 | G | A | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.971+2076G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552822 | |||||||
chr2:156552894 | C | CT | 15 | a0001c0001t0001g0027 a0001c0001t0001g0058 a0001c0001t0001g0064 others(12): Show |
15 | HG00438.hp1 HG00673.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.971+2171dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 156552894 | ||||||
chr2:156552894 | CT | C | 16 | a0001c0001t0001g0023 a0001c0001t0001g0139 a0001c0001t0001g0143 others(13): Show |
16 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.971+2171delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 156552894 | ||||||
chr2:156552894 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0016g0049 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.971+2160_971+2171d others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 156552894 | ||||||
chr2:156552960 | T | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(176): Show |
179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.971+2214T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552960 | |||||||
chr2:156552986 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(179): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.971+2240A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156552986 | |||||||
chr2:156553048 | C | T | 1 | a0002c0002t0002g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.971+2302C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553048 | |||||||
chr2:156553439 | A | G | 1 | a0001c0001t0005g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.971+2693A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553439 | |||||||
chr2:156553492 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.971+2746G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553492 | |||||||
chr2:156553595 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.971+2849C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553595 | |||||||
chr2:156553597 | C | G | 85 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(82): Show |
85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.971+2851C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553597 | |||||||
chr2:156553616 | C | G | 8 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0100 others(5): Show |
8 | HG00438.hp1 HG02071.hp2 NA19004.hp1 others(5): Show |
intron_variant | MODIFIER | c.971+2870C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553616 | |||||||
chr2:156553671 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.971+2925T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553671 | |||||||
chr2:156553688 | A | T | 12 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(9): Show |
12 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.971+2942A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553688 | |||||||
chr2:156553718 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.971+2972A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553718 | |||||||
chr2:156553784 | G | A | 1 | a0001c0001t0017g0135 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.971+3038G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553784 | |||||||
chr2:156553961 | C | A | 2 | a0002c0002t0004g0140 a0002c0002t0004g0141 |
2 | NA18952.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.971+3215C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156553961 | |||||||
chr2:156554131 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.972-3258C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554131 | |||||||
chr2:156554164 | C | A | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.972-3225C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554164 | |||||||
chr2:156554188 | G | C | 1 | a0002c0002t0002g0086 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.972-3201G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554188 | |||||||
chr2:156554378 | T | A | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.972-3011T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554378 | |||||||
chr2:156554485 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.972-2904A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554485 | |||||||
chr2:156554486 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(182): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.972-2903C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554486 | |||||||
chr2:156554839 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.972-2550A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554839 | |||||||
chr2:156554953 | G | A | 1 | a0001c0001t0013g0115 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.972-2436G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554953 | |||||||
chr2:156554980 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.972-2409A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156554980 | |||||||
chr2:156555031 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.972-2358C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555031 | |||||||
chr2:156555139 | A | G | 1 | a0001c0001t0003g0147 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.972-2250A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555139 | |||||||
chr2:156555334 | A | G | 1 | a0002c0002t0002g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.972-2055A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555334 | |||||||
chr2:156555456 | A | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.972-1933A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555456 | |||||||
chr2:156555498 | G | T | 85 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(82): Show |
85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.972-1891G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555498 | |||||||
chr2:156555849 | C | T | 1 | a0001c0001t0010g0019 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.972-1540C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156555849 | |||||||
chr2:156556350 | A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.972-1039A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156556350 | |||||||
chr2:156556586 | C | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.972-803C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156556586 | |||||||
chr2:156556996 | G | A | 1 | a0001c0001t0005g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.972-393G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156556996 | |||||||
chr2:156557009 | T | C | 1 | a0002c0002t0002g0091 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.972-380T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156557009 | |||||||
chr2:156557238 | T | C | 1 | a0003c0003t0007g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.972-151T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156557238 | |||||||
chr2:156557239 | T | C | 21 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0003g0001 others(18): Show |
21 | HG00558.hp1 HG00639.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.972-150T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 8/16 | chr2 | 156557239 | |||||||
chr2:156557615 | G | C | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165+33G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156557615 | |||||||
chr2:156557743 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1165+161G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156557743 | |||||||
chr2:156558183 | C | T | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165+601C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558183 | |||||||
chr2:156558277 | C | G | 1 | a0002c0002t0008g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1165+695C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558277 | |||||||
chr2:156558441 | G | T | 26 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(23): Show |
26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1165+859G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558441 | |||||||
chr2:156558568 | A | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1165+986A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558568 | |||||||
chr2:156558765 | C | CT | 18 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0003g0001 others(15): Show |
18 | HG00673.hp2 HG01358.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.1165+1214dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | ||||||
chr2:156558765 | C | CTT | 7 | a0002c0002t0012g0074 a0003c0003t0005g0158 a0003c0003t0007g0163 others(4): Show |
7 | HG01891.hp2 HG02886.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1165+1213_1165+121 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | ||||||
chr2:156558765 | C | CTTTTT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(25): Show |
28 | HG01109.hp1 HG01256.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1165+1210_1165+121 others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | ||||||
chr2:156558765 | C | CTTTTTT | 17 | a0001c0001t0001g0191 a0001c0001t0001g0200 a0001c0001t0001g0201 others(14): Show |
17 | HG00140.hp2 HG00544.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.1165+1209_1165+121 others(10): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | ||||||
chr2:156558765 | C | CTTTTTTT | 8 | a0001c0001t0001g0197 a0001c0001t0001g0213 a0001c0001t0001g0230 others(5): Show |
8 | HG00323.hp1 HG01433.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1165+1208_1165+121 others(11): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | ||||||
chr2:156558765 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0212 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1165+1204_1165+121 others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | ||||||
chr2:156558765 | CT | C | 81 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(78): Show |
81 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1165+1214delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | ||||||
chr2:156558765 | CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0006g0155 a0002c0002t0006g0156 |
2 | HG00735.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1165+1204_1165+121 others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156558765 | ||||||
chr2:156558871 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1165+1289C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558871 | |||||||
chr2:156558962 | C | A | 1 | a0002c0002t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1165+1380C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156558962 | |||||||
chr2:156559124 | T | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1165+1542T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559124 | |||||||
chr2:156559203 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1165+1621T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559203 | |||||||
chr2:156559485 | T | A | 1 | a0003c0003t0007g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1165+1903T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559485 | |||||||
chr2:156559523 | C | T | 184 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1165+1941C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559523 | |||||||
chr2:156559548 | A | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0220 |
2 | HG01109.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1165+1966A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559548 | |||||||
chr2:156559641 | T | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(53): Show |
56 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1165+2059T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156559641 | |||||||
chr2:156560199 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0145 a0001c0001t0017g0135 |
3 | HG02683.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1165+2617A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156560199 | |||||||
chr2:156560300 | TG | T | 175 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1165+2720delG | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156560300 | ||||||
chr2:156560581 | A | G | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1165+2999A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156560581 | |||||||
chr2:156560988 | T | C | 1 | a0001c0001t0003g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1165+3406T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156560988 | |||||||
chr2:156561034 | A | G | 1 | a0001c0001t0005g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1165+3452A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561034 | |||||||
chr2:156561040 | C | CT | 45 | a0002c0002t0002g0013 a0002c0002t0002g0020 a0002c0002t0002g0030 others(42): Show |
45 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1165+3483dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTT | 7 | a0002c0002t0002g0065 a0002c0002t0002g0066 a0002c0002t0004g0121 others(4): Show |
7 | HG00735.hp1 HG01099.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1165+3482_1165+348 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0126 a0001c0001t0003g0071 a0001c0001t0003g0072 others(8): Show |
11 | HG00639.hp1 HG01884.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.1165+3474_1165+348 others(14): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTTTTTTT others(4): Show |
30 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0056 others(27): Show |
30 | HG00639.hp2 HG01070.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.1165+3473_1165+348 others(15): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTTTTTTT others(5): Show |
59 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0023 others(56): Show |
59 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1165+3472_1165+348 others(16): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTTTTTTT others(6): Show |
42 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(39): Show |
42 | HG00140.hp2 HG00323.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1165+3471_1165+348 others(17): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTTTTTTT others(7): Show |
19 | a0001c0001t0001g0018 a0001c0001t0001g0070 a0001c0001t0001g0073 others(16): Show |
19 | HG00741.hp1 HG00741.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.1165+3470_1165+348 others(18): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTTTTTTT others(8): Show |
5 | a0001c0001t0001g0064 a0001c0001t0001g0237 a0001c0001t0001g0238 others(2): Show |
5 | HG01261.hp2 NA19000.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.1165+3469_1165+348 others(19): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0253 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1165+3468_1165+348 others(20): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0197 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1165+3467_1165+348 others(21): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1165+3465_1165+348 others(23): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561040 | C | CTTTTTTT others(13): Show |
1 | a0001c0007t0001g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1165+3464_1165+348 others(24): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156561040 | ||||||
chr2:156561193 | A | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(182): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1165+3611A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561193 | |||||||
chr2:156561209 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1165+3627G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561209 | |||||||
chr2:156561253 | G | T | 4 | a0002c0002t0004g0083 a0002c0002t0004g0121 a0002c0002t0004g0140 others(1): Show |
4 | NA18952.hp2 NA18999.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165+3671G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561253 | |||||||
chr2:156561293 | G | A | 84 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1165+3711G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561293 | |||||||
chr2:156561473 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1165+3891A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561473 | |||||||
chr2:156561601 | G | T | 2 | a0002c0002t0014g0067 a0002c0002t0014g0078 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1165+4019G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156561601 | |||||||
chr2:156562114 | A | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1165+4532A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156562114 | |||||||
chr2:156562584 | AC | A | 180 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1165+5007delC | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156562584 | ||||||
chr2:156562585 | C | A | 6 | a0001c0001t0001g0060 a0001c0001t0001g0144 a0001c0001t0001g0197 others(3): Show |
6 | HG00673.hp2 HG02630.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165+5003C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156562585 | |||||||
chr2:156562627 | G | T | 1 | a0001c0001t0001g0192 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1165+5045G>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156562627 | |||||||
chr2:156562764 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1165+5182T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156562764 | |||||||
chr2:156563126 | A | G | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1165+5544A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156563126 | |||||||
chr2:156563714 | G | A | 1 | a0001c0001t0005g0055 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1166-5111G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156563714 | |||||||
chr2:156563962 | C | A | 5 | a0001c0001t0001g0200 a0001c0001t0001g0220 a0001c0001t0001g0227 others(2): Show |
5 | HG01109.hp1 HG01123.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166-4863C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156563962 | |||||||
chr2:156564080 | A | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1166-4745A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564080 | |||||||
chr2:156564081 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1166-4744A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564081 | |||||||
chr2:156564226 | T | C | 1 | a0002c0002t0019g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1166-4599T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564226 | |||||||
chr2:156564340 | T | C | 2 | a0002c0002t0014g0067 a0002c0002t0014g0078 |
2 | HG01070.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1166-4485T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564340 | |||||||
chr2:156564730 | T | G | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1166-4095T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564730 | |||||||
chr2:156564829 | G | C | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1166-3996G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564829 | |||||||
chr2:156564850 | A | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1166-3975A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156564850 | |||||||
chr2:156565357 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0145 a0001c0001t0017g0135 |
3 | HG02683.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1166-3468C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565357 | |||||||
chr2:156565400 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1166-3425C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565400 | |||||||
chr2:156565491 | G | A | 1 | a0002c0002t0002g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1166-3334G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565491 | |||||||
chr2:156565552 | A | G | 1 | a0001c0001t0016g0049 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1166-3273A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565552 | |||||||
chr2:156565633 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(180): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1166-3192C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565633 | |||||||
chr2:156565659 | T | C | 1 | a0002c0002t0002g0086 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1166-3166T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156565659 | |||||||
chr2:156565831 | GGTTTT | G | 84 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1166-2988_1166-298 others(9): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 156565831 | ||||||
chr2:156566067 | G | C | 1 | a0001c0001t0005g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1166-2758G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566067 | |||||||
chr2:156566154 | C | T | 84 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
84 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1166-2671C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566154 | |||||||
chr2:156566295 | A | G | 1 | a0002c0002t0019g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1166-2530A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566295 | |||||||
chr2:156566564 | G | A | 7 | a0003c0003t0007g0012 a0003c0003t0007g0063 a0003c0003t0007g0163 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1166-2261G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566564 | |||||||
chr2:156566658 | G | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(181): Show |
184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1166-2167G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566658 | |||||||
chr2:156566805 | T | C | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1166-2020T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566805 | |||||||
chr2:156566866 | T | C | 85 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(82): Show |
85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1166-1959T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156566866 | |||||||
chr2:156567071 | G | C | 7 | a0003c0003t0007g0012 a0003c0003t0007g0063 a0003c0003t0007g0163 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1166-1754G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567071 | |||||||
chr2:156567110 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1166-1715A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567110 | |||||||
chr2:156567240 | G | A | 1 | a0002c0002t0019g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1166-1585G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567240 | |||||||
chr2:156567306 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1166-1519T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567306 | |||||||
chr2:156567394 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1166-1431C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567394 | |||||||
chr2:156567574 | C | T | 7 | a0003c0003t0007g0012 a0003c0003t0007g0063 a0003c0003t0007g0163 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1166-1251C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567574 | |||||||
chr2:156567614 | C | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0109 |
2 | NA19060.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1166-1211C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567614 | |||||||
chr2:156567670 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1166-1155C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567670 | |||||||
chr2:156567947 | C | T | 1 | a0002c0002t0001g0182 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1166-878C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156567947 | |||||||
chr2:156568025 | T | C | 12 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0018 others(9): Show |
12 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1166-800T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568025 | |||||||
chr2:156568059 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1166-766G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568059 | |||||||
chr2:156568450 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1166-375T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568450 | |||||||
chr2:156568466 | C | T | 5 | a0002c0002t0006g0154 a0002c0002t0006g0155 a0002c0002t0006g0156 others(2): Show |
5 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166-359C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568466 | |||||||
chr2:156568585 | A | G | 2 | a0002c0002t0001g0181 a0002c0002t0001g0183 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1166-240A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568585 | |||||||
chr2:156568719 | C | G | 2 | a0002c0002t0004g0044 a0002c0002t0004g0045 |
2 | NA19057.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1166-106C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 9/16 | chr2 | 156568719 | |||||||
chr2:156568990 | C | CT | 181 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1300+47dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 156568990 | ||||||
chr2:156569100 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0105 |
2 | NA19067.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1300+141A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 10/16 | chr2 | 156569100 | |||||||
chr2:156569223 | T | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0038 others(3): Show |
6 | HG00741.hp2 HG01192.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1301-140T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 10/16 | chr2 | 156569223 | |||||||
chr2:156569289 | A | G | 26 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(23): Show |
26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1301-74A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 10/16 | chr2 | 156569289 | |||||||
chr2:156569306 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1301-57A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 10/16 | chr2 | 156569306 | |||||||
chr2:156569602 | ACTGGCAG others(4): Show |
A | 19 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(16): Show |
19 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1476+66_1476+76del others(11): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 156569602 | ||||||
chr2:156569605 | G | A | 1 | a0002c0002t0002g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1476+67G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 11/16 | chr2 | 156569605 | |||||||
chr2:156570052 | C | T | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1477-35C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 11/16 | chr2 | 156570052 | |||||||
chr2:156570359 | T | C | 1 | a0002c0002t0002g0138 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1608+141T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570359 | |||||||
chr2:156570410 | A | T | 1 | a0002c0002t0004g0141 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1608+192A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570410 | |||||||
chr2:156570486 | A | G | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1608+268A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570486 | |||||||
chr2:156570553 | T | G | 1 | a0002c0002t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1608+335T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570553 | |||||||
chr2:156570671 | T | A | 1 | a0002c0002t0002g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1608+453T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570671 | |||||||
chr2:156570775 | G | A | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1609-359G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570775 | |||||||
chr2:156570810 | A | T | 86 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(83): Show |
86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1609-324A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156570810 | |||||||
chr2:156571081 | T | C | 248 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(245): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1609-53T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 12/16 | chr2 | 156571081 | |||||||
chr2:156571325 | C | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1767+33C>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571325 | |||||||
chr2:156571338 | G | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(172): Show |
175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1767+46G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571338 | |||||||
chr2:156571743 | TAC | T | 83 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(80): Show |
83 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1767+462_1767+463d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156571743 | ||||||
chr2:156571754 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1767+462A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571754 | |||||||
chr2:156571756 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1767+464G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571756 | |||||||
chr2:156571823 | T | A | 64 | a0002c0002t0001g0194 a0002c0002t0002g0013 a0002c0002t0002g0020 others(61): Show |
64 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1767+531T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571823 | |||||||
chr2:156571882 | A | C | 64 | a0002c0002t0001g0194 a0002c0002t0002g0013 a0002c0002t0002g0020 others(61): Show |
64 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1767+590A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571882 | |||||||
chr2:156571963 | C | G | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1767+671C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156571963 | |||||||
chr2:156572095 | C | T | 1 | a0001c0001t0005g0166 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1767+803C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572095 | |||||||
chr2:156572154 | C | G | 85 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(82): Show |
85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1767+862C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572154 | |||||||
chr2:156572191 | T | C | 8 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
8 | HG00639.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767+899T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572191 | |||||||
chr2:156572220 | G | A | 1 | a0002c0002t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1767+928G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572220 | |||||||
chr2:156572253 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1767+961C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572253 | |||||||
chr2:156572297 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1767+1005G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572297 | |||||||
chr2:156572389 | G | A | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767+1097G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572389 | |||||||
chr2:156572576 | G | C | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767+1284G>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572576 | |||||||
chr2:156572649 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1767+1357G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572649 | |||||||
chr2:156572786 | T | G | 6 | a0002c0002t0001g0194 a0002c0002t0009g0034 a0002c0002t0009g0118 others(3): Show |
6 | HG01346.hp2 HG01433.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1767+1494T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156572786 | |||||||
chr2:156573065 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1767+1773G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573065 | |||||||
chr2:156573220 | T | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0145 a0001c0001t0017g0135 |
3 | HG02683.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1767+1928T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573220 | |||||||
chr2:156573274 | A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1767+1982A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573274 | |||||||
chr2:156573645 | A | G | 42 | a0002c0002t0002g0013 a0002c0002t0002g0020 a0002c0002t0002g0030 others(39): Show |
42 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1767+2353A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573645 | |||||||
chr2:156573776 | C | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1767+2484C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573776 | |||||||
chr2:156573893 | G | A | 7 | a0003c0003t0007g0012 a0003c0003t0007g0063 a0003c0003t0007g0163 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1767+2601G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573893 | |||||||
chr2:156573920 | C | T | 248 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(245): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1767+2628C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156573920 | |||||||
chr2:156574020 | T | A | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767+2728T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574020 | |||||||
chr2:156574043 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1767+2751A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574043 | |||||||
chr2:156574155 | G | A | 19 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(16): Show |
19 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1767+2863G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574155 | |||||||
chr2:156574215 | G | GA | 59 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(56): Show |
59 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1767+2934dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156574215 | ||||||
chr2:156574247 | C | T | 3 | a0001c0004t0001g0199 a0001c0004t0001g0218 a0001c0004t0001g0219 |
3 | HG00140.hp2 HG01433.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1767+2955C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574247 | |||||||
chr2:156574338 | T | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0102 |
3 | HG02109.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1767+3046T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574338 | |||||||
chr2:156574408 | C | G | 5 | a0002c0002t0006g0154 a0002c0002t0006g0155 a0002c0002t0006g0156 others(2): Show |
5 | HG00735.hp1 HG01099.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.1767+3116C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574408 | |||||||
chr2:156574557 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(245): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1767+3265A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574557 | |||||||
chr2:156574592 | AT | A | 59 | a0002c0002t0002g0013 a0002c0002t0002g0020 a0002c0002t0002g0030 others(56): Show |
59 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1767+3311delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156574592 | ||||||
chr2:156574909 | G | A | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1767+3617G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156574909 | |||||||
chr2:156575031 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1767+3739A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575031 | |||||||
chr2:156575154 | A | C | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1768-3735A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575154 | |||||||
chr2:156575176 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1768-3713C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575176 | |||||||
chr2:156575206 | A | G | 1 | a0002c0002t0009g0137 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1768-3683A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575206 | |||||||
chr2:156575243 | A | G | 63 | a0002c0002t0002g0013 a0002c0002t0002g0020 a0002c0002t0002g0030 others(60): Show |
63 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1768-3646A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575243 | |||||||
chr2:156575402 | CT | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(226): Show |
229 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.1768-3469delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156575402 | ||||||
chr2:156575402 | CTT | C | 6 | a0001c0001t0001g0131 a0001c0001t0001g0213 a0001c0001t0001g0239 others(3): Show |
6 | HG00323.hp1 HG00323.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1768-3470_1768-346 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156575402 | ||||||
chr2:156575407 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1768-3482T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575407 | |||||||
chr2:156575510 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1768-3379C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575510 | |||||||
chr2:156575523 | C | T | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1768-3366C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575523 | |||||||
chr2:156575769 | AT | A | 7 | a0003c0003t0007g0012 a0003c0003t0007g0063 a0003c0003t0007g0163 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1768-3116delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156575769 | ||||||
chr2:156575936 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1768-2953T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156575936 | |||||||
chr2:156576162 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(174): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.1768-2727G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156576162 | |||||||
chr2:156576226 | A | G | 9 | a0002c0002t0006g0039 a0002c0002t0006g0117 a0002c0002t0006g0154 others(6): Show |
9 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1768-2663A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156576226 | |||||||
chr2:156576288 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1768-2601C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156576288 | |||||||
chr2:156576466 | T | TA | 7 | a0003c0003t0007g0012 a0003c0003t0007g0063 a0003c0003t0007g0163 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1768-2409dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156576466 | ||||||
chr2:156576466 | TA | T | 157 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1768-2409delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156576466 | ||||||
chr2:156576466 | TAA | T | 16 | a0001c0001t0001g0092 a0001c0001t0001g0242 a0001c0001t0003g0001 others(13): Show |
16 | HG00558.hp1 HG01258.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.1768-2410_1768-240 others(6): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156576466 | ||||||
chr2:156576466 | TAAA | T | 61 | a0002c0002t0002g0013 a0002c0002t0002g0020 a0002c0002t0002g0030 others(58): Show |
61 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1768-2411_1768-240 others(7): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156576466 | ||||||
chr2:156576549 | T | C | 26 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(23): Show |
26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1768-2340T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156576549 | |||||||
chr2:156576744 | A | C | 1 | a0003c0003t0005g0158 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1768-2145A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156576744 | |||||||
chr2:156577006 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(245): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1768-1883A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577006 | |||||||
chr2:156577088 | G | A | 2 | a0002c0002t0002g0065 a0002c0002t0002g0066 |
2 | HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1768-1801G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577088 | |||||||
chr2:156577101 | A | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0077 |
2 | NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1768-1788A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577101 | |||||||
chr2:156577166 | C | G | 62 | a0002c0002t0002g0013 a0002c0002t0002g0020 a0002c0002t0002g0030 others(59): Show |
62 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1768-1723C>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577166 | |||||||
chr2:156577319 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0077 |
2 | NA19009.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1768-1570C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577319 | |||||||
chr2:156577338 | A | T | 9 | a0002c0002t0001g0194 a0003c0003t0005g0158 a0003c0003t0007g0012 others(6): Show |
9 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1768-1551A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577338 | |||||||
chr2:156577362 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(245): Show |
248 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.1768-1527A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577362 | |||||||
chr2:156577522 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1768-1367A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577522 | |||||||
chr2:156577777 | T | A | 1 | a0002c0002t0021g0054 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1768-1112T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577777 | |||||||
chr2:156577779 | A | C | 1 | a0002c0002t0021g0054 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1768-1110A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577779 | |||||||
chr2:156577883 | T | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(182): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1768-1006T>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156577883 | |||||||
chr2:156578372 | C | CTT | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1768-505_1768-504d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156578372 | ||||||
chr2:156578377 | T | C | 21 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0003g0001 others(18): Show |
21 | HG00558.hp1 HG00639.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.1768-512T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156578377 | |||||||
chr2:156578455 | T | C | 3 | a0002c0002t0001g0181 a0002c0002t0001g0182 a0002c0002t0001g0183 |
3 | HG03130.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1768-434T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156578455 | |||||||
chr2:156578565 | G | A | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1768-324G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156578565 | |||||||
chr2:156578622 | G | A | 1 | a0001c0001t0003g0205 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1768-267G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156578622 | |||||||
chr2:156578754 | T | C | 3 | a0002c0002t0012g0046 a0002c0002t0012g0074 a0002c0002t0012g0075 |
3 | HG02258.hp2 HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1768-135T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | chr2 | 156578754 | |||||||
chr2:156578834 | G | GA | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1768-48dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156578834 | ||||||
chr2:156578834 | GA | G | 3 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 |
3 | HG02559.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1768-48delA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 156578834 | ||||||
chr2:156579012 | TAA | T | 4 | a0002c0002t0001g0173 a0002c0002t0001g0181 a0002c0002t0001g0182 others(1): Show |
4 | HG03130.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1880+12_1880+13del others(2): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 14/16 | chr2 | 156579012 | |||||||
chr2:156579309 | A | T | 26 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(23): Show |
26 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1959+145A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 15/16 | chr2 | 156579309 | |||||||
chr2:156579310 | T | A | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1959+146T>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 15/16 | chr2 | 156579310 | |||||||
chr2:156579329 | C | CT | 7 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG00639.hp2 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1959+180dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 156579329 | ||||||
chr2:156579329 | CT | C | 27 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(24): Show |
27 | HG00558.hp1 HG00639.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1959+180delT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | 156579329 | ||||||
chr2:156579551 | C | T | 1 | a0002c0002t0019g0185 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1960-139C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 15/16 | chr2 | 156579551 | |||||||
chr2:156579967 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2058+179G>A | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156579967 | |||||||
chr2:156580237 | T | C | 2 | a0001c0001t0005g0055 a0001c0001t0005g0179 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2058+449T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156580237 | |||||||
chr2:156580454 | A | C | 8 | a0003c0003t0005g0158 a0003c0003t0007g0012 a0003c0003t0007g0063 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2058+666A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156580454 | |||||||
chr2:156580702 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2058+914C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156580702 | |||||||
chr2:156580856 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.2058+1068A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156580856 | |||||||
chr2:156581071 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0146 others(55): Show |
58 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.2058+1283T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581071 | |||||||
chr2:156581142 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2058+1354A>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581142 | |||||||
chr2:156581260 | C | T | 1 | a0002c0002t0008g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2058+1472C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581260 | |||||||
chr2:156581311 | A | AT | 4 | a0001c0001t0003g0037 a0001c0001t0003g0072 a0001c0001t0003g0076 others(1): Show |
4 | HG00639.hp1 HG01884.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.2059-1475dupT | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 156581311 | ||||||
chr2:156581500 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2059-1293C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581500 | |||||||
chr2:156581691 | T | C | 1 | a0002c0002t0001g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2059-1102T>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581691 | |||||||
chr2:156581692 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02735.hp2 HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2059-1101C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581692 | |||||||
chr2:156581847 | A | C | 2 | a0001c0001t0003g0076 a0001c0001t0003g0088 |
2 | HG00639.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.2059-946A>C | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156581847 | |||||||
chr2:156581988 | GATGTGTG others(3): Show |
G | 1 | a0001c0001t0005g0179 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2059-796_2059-787d others(12): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 156581988 | ||||||
chr2:156582453 | A | G | 1 | a0002c0002t0005g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2059-340A>G | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156582453 | |||||||
chr2:156582484 | T | TA | 103 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(100): Show |
103 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2059-293dupA | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 156582484 | ||||||
chr2:156582484 | T | TAA | 80 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0001 others(77): Show |
80 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.2059-294_2059-293d others(4): Show |
GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | 156582484 | ||||||
chr2:156582615 | C | T | 1 | a0001c0001t0013g0069 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2059-178C>T | GPD2 | ENSG00000115159.17 | transcript | ENST00000438166.7 | protein_coding | 16/16 | chr2 | 156582615 |