Item | Value |
---|---|
geneid | 5239 |
ensemblid | ENSG00000154330.13 |
hgncid | 8908 |
symbol | PGM5 |
name | phosphoglucomutase 5 |
refseq_nuc | NM_021965.4 |
refseq_prot | NP_068800.2 |
ensembl_nuc | ENST00000396396.6 |
ensembl_prot | ENSP00000379678.1 |
mane_status | MANE Select |
chr | chr9 |
start | 68356611 |
end | 68531061 |
strand | + |
ver | v1.2 |
region | chr9:68356611-68531061 |
region5000 | chr9:68351611-68536061 |
regionname0 | PGM5_chr9_68356611_68531061 |
regionname5000 | PGM5_chr9_68351611_68536061 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 567 | 239 | 70 | 42 | 89 | 12 | 24 | 61 | PGM5_chr9_68351611_68536061 | PGM5 | MEGSP others(562): Show |
chr9 | 68351611 | 68536061 |
a0002 | 0/0 | 506 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | MVVGS others(501): Show |
chr9 | 68351611 | 68536061 |
a0003 | 0/0 | 567 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | MEGSP others(562): Show |
chr9 | 68351611 | 68536061 |
a0004 | 0/0 | 567 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | MEGSP others(562): Show |
chr9 | 68351611 | 68536061 |
a0005 | 0/0 | 567 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | MEGSP others(562): Show |
chr9 | 68351611 | 68536061 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1701 | 149 | 43 | 21 | 56 | 7 | 21 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0002 | 0/1 | 1701 | 55 | 5 | 17 | 26 | 3 | 3 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0003 | 0/0 | 1701 | 10 | 2 | 2 | 4 | 2 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0004 | 0/0 | 1701 | 7 | 6 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0005 | 0/0 | 1701 | 6 | 5 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0006 | 0/0 | 1701 | 3 | 3 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0007 | 0/0 | 1701 | 2 | 2 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0011 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0012 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0014 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0016 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0017 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0019 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0001c0020 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0002c0009 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATAGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0002c0010 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATAGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0003c0008 | 0/0 | 1701 | 2 | 2 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0004c0013 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0004c0018 | 0/0 | 1701 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 | ||
a0005c0015 | 0/0 | 1701 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | ATGGA others(1696): Show |
chr9 | 68351611 | 68536061 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3625 | 53 | 10 | 9 | 27 | 3 | 4 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0002 | 0/0 | 3625 | 8 | 3 | 0 | 2 | 2 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0003 | 0/0 | 3625 | 18 | 2 | 4 | 3 | 1 | 8 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0004 | 1/0 | 3626 | 10 | 8 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0005 | 0/0 | 3626 | 9 | 1 | 0 | 8 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0006 | 0/0 | 3626 | 5 | 1 | 2 | 0 | 1 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0007 | 0/0 | 3626 | 8 | 7 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0008 | 0/0 | 3626 | 2 | 0 | 0 | 2 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0009 | 0/0 | 3626 | 2 | 1 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0010 | 0/0 | 3626 | 7 | 0 | 0 | 5 | 0 | 2 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0011 | 0/0 | 3625 | 6 | 0 | 1 | 5 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0012 | 0/0 | 3626 | 4 | 1 | 0 | 0 | 0 | 3 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0014 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0015 | 0/0 | 3626 | 3 | 3 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0017 | 0/0 | 3626 | 2 | 0 | 0 | 0 | 0 | 2 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0018 | 0/0 | 3625 | 2 | 0 | 2 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0019 | 0/0 | 3626 | 2 | 2 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0020 | 0/0 | 3626 | 2 | 2 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0021 | 0/0 | 3625 | 2 | 0 | 2 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0028 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0029 | 0/0 | 3625 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0001t0031 | 0/0 | 3625 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0002t0001 | 0/0 | 3625 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0002t0002 | 0/1 | 3625 | 44 | 3 | 13 | 23 | 2 | 2 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0002t0008 | 0/0 | 3626 | 5 | 1 | 0 | 3 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0002t0013 | 0/0 | 3625 | 4 | 0 | 4 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0002t0023 | 0/0 | 3625 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0003t0001 | 0/0 | 3625 | 4 | 0 | 0 | 4 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0003t0005 | 0/0 | 3626 | 4 | 0 | 2 | 0 | 2 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0003t0009 | 0/0 | 3626 | 2 | 2 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0004t0002 | 0/0 | 3625 | 3 | 3 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0004t0006 | 0/0 | 3626 | 2 | 2 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0004t0024 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0004t0025 | 0/0 | 3626 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0005t0004 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0005t0009 | 0/0 | 3626 | 3 | 2 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0005t0014 | 0/0 | 3626 | 2 | 2 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0006t0001 | 0/0 | 3625 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0006t0004 | 0/0 | 3626 | 2 | 2 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0007t0004 | 0/0 | 3626 | 2 | 2 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0011t0002 | 0/0 | 3625 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0012t0001 | 0/0 | 3625 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0014t0004 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0016t0022 | 0/0 | 3625 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0001c0017t0004 | 0/0 | 3626 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0019t0006 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0001c0020t0030 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0002c0009t0016 | 0/0 | 3625 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0002c0010t0016 | 0/0 | 3625 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0003c0008t0026 | 0/0 | 3611 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3606): Show |
chr9 | 68351611 | 68536061 |
a0003c0008t0027 | 0/0 | 3611 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3606): Show |
chr9 | 68351611 | 68536061 |
a0004c0013t0001 | 0/0 | 3625 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3620): Show |
chr9 | 68351611 | 68536061 |
a0004c0018t0006 | 0/0 | 3626 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
a0005c0015t0012 | 0/0 | 3626 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | GCACT others(3621): Show |
chr9 | 68351611 | 68536061 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0004g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0006g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0007g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0007g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0009g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0009g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0010g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0010g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0010g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0010g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0010g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0010g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0010g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0011g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0011g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0011g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0011g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0011g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0011g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0012g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0012g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0012g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0012g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0014g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0015g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0015g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0015g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0017g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0017g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0018g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0018g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0019g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0019g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0020g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0020g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0021g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0021g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0028g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0029g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0001t0031g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0022 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0008g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0008g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0008g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0013g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0013g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0013g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0013g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0002t0023g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0003t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0003t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0003t0005g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0003t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0003t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0003t0009g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0003t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0004t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0004t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0004t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0004t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0004t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0004t0024g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0004t0025g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0005t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0005t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0005t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0005t0009g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0005t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0005t0014g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0006t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0006t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0006t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0007t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0007t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0011t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0012t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0014t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0016t0022g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0017t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0019t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0001c0020t0030g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0002c0009t0016g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0002c0010t0016g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0003c0008t0026g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0003c0008t0027g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0004c0013t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0004c0018t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
a0005c0015t0012g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0205 | EUR | GBR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0021 | EUR | GBR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00280 | hp1 | a0001 | c0002 | t0023 | g0061 | EUR | FIN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00280 | hp2 | a0001 | c0001 | t0006 | g0079 | EUR | FIN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0071 | EUR | FIN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00323 | hp2 | a0001 | c0003 | t0005 | g0020 | EUR | FIN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00408 | hp1 | a0001 | c0001 | t0010 | g0214 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00423 | hp2 | a0002 | c0009 | t0016 | g0246 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00597 | hp1 | a0001 | c0001 | t0007 | g0167 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00597 | hp2 | a0001 | c0002 | t0008 | g0025 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00609 | hp2 | a0001 | c0001 | t0008 | g0078 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00642 | hp1 | a0001 | c0003 | t0005 | g0007 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00735 | hp1 | a0001 | c0002 | t0013 | g0045 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00735 | hp2 | a0001 | c0001 | t0021 | g0207 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG00741 | hp2 | a0001 | c0002 | t0013 | g0046 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0059 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01081 | hp1 | a0001 | c0003 | t0005 | g0013 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01106 | hp2 | a0001 | c0002 | t0013 | g0047 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0063 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0075 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0076 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01175 | hp1 | a0001 | c0004 | t0025 | g0236 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01255 | hp2 | a0001 | c0005 | t0009 | g0210 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01261 | hp2 | a0001 | c0001 | t0018 | g0226 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01346 | hp2 | a0001 | c0002 | t0013 | g0048 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01433 | hp1 | a0001 | c0001 | t0021 | g0134 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01433 | hp2 | a0001 | c0001 | t0011 | g0219 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01891 | hp1 | a0001 | c0001 | t0019 | g0002 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01891 | hp2 | a0001 | c0004 | t0002 | g0242 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PEL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0217 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02055 | hp1 | a0001 | c0001 | t0015 | g0116 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02055 | hp2 | a0001 | c0001 | t0012 | g0231 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02056 | hp1 | a0001 | c0012 | t0001 | g0109 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02080 | hp1 | a0001 | c0001 | t0011 | g0215 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02080 | hp2 | a0005 | c0015 | t0012 | g0152 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02083 | hp1 | a0001 | c0017 | t0004 | g0069 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0135 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02148 | hp1 | a0001 | c0001 | t0018 | g0227 | AMR | PEL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PEL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | CDX | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02257 | hp1 | a0001 | c0004 | t0006 | g0244 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0105 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02451 | hp1 | a0001 | c0001 | t0020 | g0156 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02451 | hp2 | a0001 | c0006 | t0004 | g0122 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02523 | hp1 | a0001 | c0002 | t0008 | g0034 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02572 | hp1 | a0001 | c0001 | t0009 | g0119 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02622 | hp1 | a0001 | c0020 | t0030 | g0090 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0171 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0085 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02647 | hp2 | a0001 | c0016 | t0022 | g0084 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02698 | hp1 | a0001 | c0001 | t0006 | g0077 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02698 | hp2 | a0001 | c0001 | t0012 | g0118 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0169 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02809 | hp2 | a0001 | c0007 | t0004 | g0091 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02895 | hp1 | a0001 | c0003 | t0009 | g0230 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02895 | hp2 | a0001 | c0005 | t0009 | g0209 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02896 | hp1 | a0001 | c0001 | t0020 | g0157 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02897 | hp1 | a0001 | c0003 | t0009 | g0229 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0232 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0233 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02965 | hp2 | a0001 | c0007 | t0004 | g0098 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02970 | hp1 | a0001 | c0001 | t0014 | g0094 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02970 | hp2 | a0001 | c0004 | t0002 | g0243 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03041 | hp1 | a0001 | c0005 | t0004 | g0089 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03041 | hp2 | a0004 | c0018 | t0006 | g0237 | AFR | GWD | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0165 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03195 | hp1 | a0001 | c0019 | t0006 | g0239 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03209 | hp1 | a0001 | c0006 | t0001 | g0092 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03209 | hp2 | a0003 | c0008 | t0026 | g0234 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03486 | hp1 | a0004 | c0013 | t0001 | g0146 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03486 | hp2 | a0001 | c0005 | t0009 | g0208 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03490 | hp1 | a0001 | c0001 | t0017 | g0222 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0027 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03492 | hp2 | a0001 | c0001 | t0017 | g0221 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03516 | hp1 | a0001 | c0004 | t0024 | g0240 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03516 | hp2 | a0001 | c0001 | t0015 | g0097 | AFR | ESN | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0113 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03654 | hp1 | a0001 | c0001 | t0012 | g0153 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0194 | SAS | BEB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | BEB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03942 | hp2 | a0001 | c0002 | t0008 | g0065 | SAS | BEB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG04199 | hp1 | a0001 | c0001 | t0010 | g0224 | SAS | STU | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0170 | SAS | STU | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0193 | SAS | STU | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG04204 | hp2 | a0001 | c0001 | t0012 | g0187 | SAS | STU | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0206 | SAS | STU | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | STU | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18522 | hp1 | a0001 | c0006 | t0004 | g0107 | AFR | YRI | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | YRI | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18612 | hp1 | a0001 | c0001 | t0009 | g0211 | EAS | CHB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0168 | AFR | YRI | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18906 | hp2 | a0001 | c0004 | t0002 | g0238 | AFR | YRI | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18952 | hp2 | a0001 | c0011 | t0002 | g0033 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18961 | hp1 | a0001 | c0001 | t0010 | g0228 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18963 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18965 | hp1 | a0001 | c0001 | t0008 | g0081 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18980 | hp2 | a0001 | c0001 | t0010 | g0216 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0149 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18992 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18994 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18994 | hp2 | a0001 | c0001 | t0011 | g0225 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19003 | hp2 | a0002 | c0010 | t0016 | g0245 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19005 | hp2 | a0001 | c0001 | t0010 | g0223 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19009 | hp1 | a0001 | c0001 | t0011 | g0213 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19030 | hp2 | a0001 | c0002 | t0008 | g0044 | AFR | LWK | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0188 | AFR | LWK | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | LWK | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19063 | hp2 | a0001 | c0001 | t0029 | g0111 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19067 | hp1 | a0001 | c0001 | t0011 | g0212 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19067 | hp2 | a0001 | c0002 | t0008 | g0029 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19075 | hp2 | a0001 | c0001 | t0031 | g0126 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19081 | hp2 | a0001 | c0001 | t0011 | g0218 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19086 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA20129 | hp1 | a0001 | c0005 | t0014 | g0088 | AFR | ASW | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA20129 | hp2 | a0001 | c0004 | t0006 | g0241 | AFR | ASW | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0072 | EUR | TSI | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | TSI | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0050 | EUR | TSI | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA20805 | hp2 | a0001 | c0003 | t0005 | g0012 | EUR | TSI | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA20905 | hp1 | a0001 | c0001 | t0010 | g0220 | SAS | GIH | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02109 | hp1 | a0003 | c0008 | t0027 | g0235 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0155 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02559 | hp1 | a0001 | c0001 | t0028 | g0040 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG02559 | hp2 | a0001 | c0014 | t0004 | g0018 | AFR | ACB | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG03471 | hp2 | a0001 | c0001 | t0019 | g0001 | AFR | MSL | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG06807 | hp1 | a0001 | c0005 | t0014 | g0087 | AFR | USA | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | USA | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0022 | REF | REF | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0125 | REF | REF | PGM5_chr9_68351611_68536061 | PGM5 | chr9 | 68351611 | 68536061 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:68357130 | G | A | 1 | a0002 | 2 | HG00423.hp2 NA19003.hp2 |
start_lost | HIGH | c.3G>A | p.Met1? | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 520/3626 | 3/1704 | 1/567 | chr9 | 68357130 | |||
chr9:68357149 | G | T | 1 | a0003 | 2 | HG02109.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.22G>T | p.Val8Leu | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 539/3626 | 22/1704 | 8/567 | chr9 | 68357149 | |||
chr9:68357191 | G | T | 1 | a0002 | 2 | HG00423.hp2 NA19003.hp2 |
missense_variant | MODERATE | c.64G>T | p.Ala22Ser | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 581/3626 | 64/1704 | 22/567 | chr9 | 68357191 | |||
chr9:68392431 | G | A | 1 | a0004 | 2 | HG03041.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.1001G>A | p.Arg334His | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/11 | 1518/3626 | 1001/1704 | 334/567 | chr9 | 68392431 | |||
chr9:68499332 | G | A | 1 | a0005 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1585G>A | p.Asp529Asn | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/11 | 2102/3626 | 1585/1704 | 529/567 | chr9 | 68499332 | |||
chr9:68529654 | T | C | 1 | a0001 | 1 | NA19063.hp2 | stop_lost | HIGH | c.1702T>C | p.Ter568Argext*? | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 11/11 | 2219/3626 | 1702/1704 | 568/567 | chr9 | 68529654 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:68357169 | G | A | 2 | a0002c0009 a0002c0010 |
2 | HG00423.hp2 NA19003.hp2 |
synonymous_variant | LOW | c.42G>A | p.Ala14Ala | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 559/3626 | 42/1704 | 14/567 | chr9 | 68357169 | |||
chr9:68357172 | C | T | 1 | a0001c0020 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.45C>T | p.Pro15Pro | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 562/3626 | 45/1704 | 15/567 | chr9 | 68357172 | |||
chr9:68357193 | C | T | 3 | a0001c0004 a0001c0019 a0004c0018 |
9 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
synonymous_variant | LOW | c.66C>T | p.Ala22Ala | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 583/3626 | 66/1704 | 22/567 | chr9 | 68357193 | |||
chr9:68378237 | G | A | 3 | a0001c0006 a0001c0007 a0001c0020 |
6 | HG02451.hp2 HG02622.hp1 HG02809.hp2 others(3): Show |
synonymous_variant | LOW | c.300G>A | p.Ser100Ser | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/11 | 817/3626 | 300/1704 | 100/567 | chr9 | 68378237 | |||
chr9:68378303 | C | T | 3 | a0001c0003 a0001c0016 a0001c0017 |
12 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(9): Show |
synonymous_variant | LOW | c.366C>T | p.Ser122Ser | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/11 | 883/3626 | 366/1704 | 122/567 | chr9 | 68378303 | |||
chr9:68384399 | T | C | 7 | a0001c0002 a0001c0004 a0001c0007 others(4): Show |
67 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(64): Show |
splice_region_variant&synonymous_variant | LOW | c.426T>C | p.Gly142Gly | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/11 | 943/3626 | 426/1704 | 142/567 | chr9 | 68384399 | |||
chr9:68384537 | A | G | 1 | a0001c0005 | 6 | HG01255.hp2 HG02895.hp2 HG03041.hp1 others(3): Show |
synonymous_variant | LOW | c.564A>G | p.Pro188Pro | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/11 | 1081/3626 | 564/1704 | 188/567 | chr9 | 68384537 | |||
chr9:68387467 | G | A | 2 | a0001c0004 a0004c0018 |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
synonymous_variant | LOW | c.576G>A | p.Glu192Glu | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/11 | 1093/3626 | 576/1704 | 192/567 | chr9 | 68387467 | |||
chr9:68387548 | A | G | 1 | a0001c0017 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.657A>G | p.Gly219Gly | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/11 | 1174/3626 | 657/1704 | 219/567 | chr9 | 68387548 | |||
chr9:68387578 | A | G | 1 | a0001c0016 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.687A>G | p.Ala229Ala | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/11 | 1204/3626 | 687/1704 | 229/567 | chr9 | 68387578 | |||
chr9:68392411 | T | C | 1 | a0001c0012 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.981T>C | p.Tyr327Tyr | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/11 | 1498/3626 | 981/1704 | 327/567 | chr9 | 68392411 | |||
chr9:68479422 | T | C | 1 | a0001c0014 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1164T>C | p.Ser388Ser | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/11 | 1681/3626 | 1164/1704 | 388/567 | chr9 | 68479422 | |||
chr9:68529593 | C | T | 1 | a0001c0011 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.1641C>T | p.Ile547Ile | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 11/11 | 2158/3626 | 1641/1704 | 547/567 | chr9 | 68529593 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:68356620 | G | A | 2 | a0002c0009t0016 a0002c0010t0016 |
2 | HG00423.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-508G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 508 | chr9 | 68356620 | ||||||
chr9:68356626 | C | T | 2 | a0002c0009t0016 a0002c0010t0016 |
2 | HG00423.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-502C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 502 | chr9 | 68356626 | ||||||
chr9:68356646 | C | G | 1 | a0001c0001t0031 | 1 | NA19075.hp2 | 5_prime_UTR_variant | MODIFIER | c.-482C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 482 | chr9 | 68356646 | ||||||
chr9:68356657 | C | A | 1 | a0001c0001t0017 | 2 | HG03490.hp1 HG03492.hp2 |
5_prime_UTR_variant | MODIFIER | c.-471C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 471 | chr9 | 68356657 | ||||||
chr9:68356702 | G | A | 2 | a0002c0009t0016 a0002c0010t0016 |
2 | HG00423.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-426G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 426 | chr9 | 68356702 | ||||||
chr9:68356712 | C | A | 1 | a0001c0002t0013 | 4 | HG00735.hp1 HG00741.hp2 HG01106.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-416C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 416 | chr9 | 68356712 | ||||||
chr9:68356712 | C | T | 2 | a0002c0009t0016 a0002c0010t0016 |
2 | HG00423.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-416C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 416 | chr9 | 68356712 | ||||||
chr9:68356728 | T | G | 2 | a0002c0009t0016 a0002c0010t0016 |
2 | HG00423.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-400T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 400 | chr9 | 68356728 | ||||||
chr9:68356787 | G | A | 1 | a0001c0016t0022 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-341G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 341 | chr9 | 68356787 | ||||||
chr9:68356812 | C | T | 2 | a0002c0009t0016 a0002c0010t0016 |
2 | HG00423.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-316C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 316 | chr9 | 68356812 | ||||||
chr9:68356851 | G | C | 2 | a0002c0009t0016 a0002c0010t0016 |
2 | HG00423.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-277G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 277 | chr9 | 68356851 | ||||||
chr9:68356870 | G | C | 2 | a0002c0009t0016 a0002c0010t0016 |
2 | HG00423.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-258G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 258 | chr9 | 68356870 | ||||||
chr9:68356882 | T | C | 25 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(22): Show |
107 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(104): Show |
5_prime_UTR_variant | MODIFIER | c.-246T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 246 | chr9 | 68356882 | ||||||
chr9:68356925 | A | G | 2 | a0002c0009t0016 a0002c0010t0016 |
2 | HG00423.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-203A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 203 | chr9 | 68356925 | ||||||
chr9:68356956 | GGGCGGGC others(8): Show |
G | 2 | a0003c0008t0026 a0003c0008t0027 |
2 | HG02109.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-162_-148delTCCCCA others(9): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 148 | INFO_REALIGN_3_PRIME | chr9 | 68356956 | |||||
chr9:68356969 | C | G | 5 | a0001c0001t0004 a0001c0003t0001 a0001c0003t0005 others(2): Show |
11 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-159C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 159 | chr9 | 68356969 | ||||||
chr9:68357014 | G | C | 1 | a0001c0001t0028 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-114G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 114 | chr9 | 68357014 | ||||||
chr9:68357025 | G | A | 4 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0012 others(1): Show |
31 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-103G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 103 | chr9 | 68357025 | ||||||
chr9:68357061 | A | G | 2 | a0002c0009t0016 a0002c0010t0016 |
2 | HG00423.hp2 NA19003.hp2 |
5_prime_UTR_variant | MODIFIER | c.-67A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 67 | chr9 | 68357061 | ||||||
chr9:68357096 | G | A | 16 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(13): Show |
81 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
5_prime_UTR_variant | MODIFIER | c.-32G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/11 | 32 | chr9 | 68357096 | ||||||
chr9:68530036 | A | G | 1 | a0001c0004t0025 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*380A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 11/11 | 380 | chr9 | 68530036 | ||||||
chr9:68530461 | A | G | 2 | a0001c0001t0015 a0001c0001t0019 |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*805A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 11/11 | 805 | chr9 | 68530461 | ||||||
chr9:68530463 | C | G | 9 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(6): Show |
36 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*807C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 11/11 | 807 | chr9 | 68530463 | ||||||
chr9:68530776 | G | A | 3 | a0001c0001t0018 a0001c0001t0021 a0001c0020t0030 |
5 | HG00735.hp2 HG01261.hp2 HG01433.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1120G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 11/11 | 1120 | chr9 | 68530776 | ||||||
chr9:68530818 | G | A | 1 | a0001c0002t0023 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1162G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 11/11 | 1162 | chr9 | 68530818 | ||||||
chr9:68530919 | C | T | 5 | a0001c0001t0014 a0001c0004t0024 a0001c0005t0014 others(2): Show |
6 | HG02109.hp1 HG02622.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1263C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 11/11 | 1263 | chr9 | 68530919 | ||||||
chr9:68531019 | CA | C | 21 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(18): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1364delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 11/11 | 1364 | chr9 | 68531019 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:68357407 | C | T | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+19C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357407 | |||||||
chr9:68357426 | C | T | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+38C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357426 | |||||||
chr9:68357519 | C | G | 9 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+131C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357519 | |||||||
chr9:68357552 | G | T | 2 | a0003c0008t0026g0234 a0003c0008t0027g0235 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.261+164G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357552 | |||||||
chr9:68357569 | T | C | 101 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(98): Show |
101 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.261+181T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357569 | |||||||
chr9:68357607 | C | T | 9 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+219C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357607 | |||||||
chr9:68357615 | C | G | 3 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 |
3 | HG03041.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.261+227C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357615 | |||||||
chr9:68357628 | C | G | 3 | a0001c0001t0007g0232 a0001c0001t0007g0233 a0001c0001t0012g0231 |
3 | HG02055.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.261+240C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357628 | |||||||
chr9:68357670 | C | T | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+282C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357670 | |||||||
chr9:68357776 | A | G | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+388A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357776 | |||||||
chr9:68357831 | C | T | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+443C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357831 | |||||||
chr9:68357839 | C | A | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+451C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357839 | |||||||
chr9:68357907 | C | G | 4 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0003c0008t0026g0234 others(1): Show |
4 | HG02109.hp1 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+519C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357907 | |||||||
chr9:68357912 | A | AAC | 22 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(19): Show |
22 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.261+575_261+576dup others(2): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | A | AACAC | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0015g0097 others(3): Show |
6 | HG02896.hp2 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.261+573_261+576dup others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | A | AACACAC | 3 | a0001c0001t0001g0093 a0001c0001t0014g0094 a0001c0006t0001g0092 |
3 | HG00673.hp2 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.261+571_261+576dup others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | A | AACACACA others(1): Show |
2 | a0001c0007t0004g0091 a0001c0020t0030g0090 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.261+569_261+576dup others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AAC | A | 18 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0163 others(15): Show |
18 | HG00597.hp1 HG01891.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.261+575_261+576del others(2): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AACAC | A | 32 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(29): Show |
32 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.261+573_261+576del others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AACACAC | A | 14 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(11): Show |
14 | HG00099.hp1 HG00673.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.261+571_261+576del others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AACACACA others(1): Show |
A | 10 | a0001c0001t0021g0207 a0001c0002t0002g0014 a0001c0002t0002g0015 others(7): Show |
10 | HG00323.hp2 HG00735.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.261+569_261+576del others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AACACACA others(3): Show |
A | 23 | a0001c0001t0028g0040 a0001c0002t0002g0021 a0001c0002t0002g0023 others(20): Show |
23 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(20): Show |
intron_variant | MODIFIER | c.261+567_261+576del others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AACACACA others(5): Show |
A | 38 | a0001c0001t0001g0086 a0001c0002t0002g0041 a0001c0002t0002g0042 others(35): Show |
38 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.261+565_261+576del others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AACACACA others(7): Show |
A | 3 | a0001c0001t0002g0070 a0001c0001t0009g0211 a0001c0004t0006g0244 |
3 | HG02257.hp1 HG02622.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.261+563_261+576del others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AACACACA others(9): Show |
A | 13 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(10): Show |
13 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.261+561_261+576del others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AACACACA others(11): Show |
A | 19 | a0001c0001t0002g0082 a0001c0001t0010g0214 a0001c0001t0010g0216 others(16): Show |
19 | HG00408.hp1 HG00738.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.261+559_261+576del others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AACACACA others(15): Show |
A | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.261+555_261+576del others(22): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357912 | AACACACA others(17): Show |
A | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.261+553_261+576del others(24): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68357912 | ||||||
chr9:68357954 | C | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+566C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68357954 | |||||||
chr9:68358008 | T | A | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+620T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358008 | |||||||
chr9:68358095 | A | C | 5 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+707A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358095 | |||||||
chr9:68358173 | A | G | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+785A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358173 | |||||||
chr9:68358176 | C | T | 1 | a0001c0001t0006g0008 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.261+788C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358176 | |||||||
chr9:68358202 | G | A | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+814G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358202 | |||||||
chr9:68358210 | C | T | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.261+822C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358210 | |||||||
chr9:68358272 | C | A | 3 | a0001c0001t0028g0040 a0002c0009t0016g0246 a0002c0010t0016g0245 |
3 | HG00423.hp2 HG02559.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.261+884C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358272 | |||||||
chr9:68358309 | A | G | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+921A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358309 | |||||||
chr9:68358473 | A | G | 2 | a0003c0008t0026g0234 a0003c0008t0027g0235 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.261+1085A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358473 | |||||||
chr9:68358507 | C | T | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1119C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358507 | |||||||
chr9:68358543 | A | G | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1155A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358543 | |||||||
chr9:68358544 | A | G | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1156A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358544 | |||||||
chr9:68358618 | T | C | 4 | a0001c0001t0009g0119 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+1230T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358618 | |||||||
chr9:68358674 | T | A | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1286T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358674 | |||||||
chr9:68358725 | C | T | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1337C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358725 | |||||||
chr9:68358727 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(1): Show |
4 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+1339G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358727 | |||||||
chr9:68358758 | T | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+1370T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358758 | |||||||
chr9:68358766 | T | C | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1378T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358766 | |||||||
chr9:68358774 | C | A | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1386C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358774 | |||||||
chr9:68358779 | T | C | 3 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0082 |
3 | HG00323.hp1 HG02145.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.261+1391T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358779 | |||||||
chr9:68358810 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+1422G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358810 | |||||||
chr9:68358874 | A | C | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1486A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358874 | |||||||
chr9:68358881 | G | C | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1493G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358881 | |||||||
chr9:68358995 | C | T | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1607C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68358995 | |||||||
chr9:68359029 | T | C | 2 | a0002c0009t0016g0246 a0002c0010t0016g0245 |
2 | HG00423.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.261+1641T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359029 | |||||||
chr9:68359137 | A | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+1749A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359137 | |||||||
chr9:68359176 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+1788A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359176 | |||||||
chr9:68359202 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+1814T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359202 | |||||||
chr9:68359290 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+1902G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359290 | |||||||
chr9:68359309 | G | C | 52 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(49): Show |
52 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.261+1921G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359309 | |||||||
chr9:68359406 | G | A | 2 | a0001c0002t0002g0041 a0001c0002t0002g0042 |
2 | HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.261+2018G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359406 | |||||||
chr9:68359632 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2244A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359632 | |||||||
chr9:68359671 | T | C | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.261+2283T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359671 | |||||||
chr9:68359691 | T | C | 2 | a0001c0001t0003g0120 a0001c0001t0003g0172 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.261+2303T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359691 | |||||||
chr9:68359698 | C | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2310C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359698 | |||||||
chr9:68359740 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2352C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359740 | |||||||
chr9:68359758 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2370A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359758 | |||||||
chr9:68359767 | G | A | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.261+2379G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359767 | |||||||
chr9:68359804 | T | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2416T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359804 | |||||||
chr9:68359821 | C | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2433C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359821 | |||||||
chr9:68359834 | T | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2446T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359834 | |||||||
chr9:68359867 | T | A | 3 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0002c0009t0016g0246 |
3 | HG00423.hp2 HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+2479T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359867 | |||||||
chr9:68359903 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(1): Show |
4 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+2515G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68359903 | |||||||
chr9:68360001 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2613T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360001 | |||||||
chr9:68360002 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2614G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360002 | |||||||
chr9:68360080 | A | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+2692A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360080 | |||||||
chr9:68360105 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2717A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360105 | |||||||
chr9:68360180 | A | G | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.261+2792A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360180 | |||||||
chr9:68360224 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2836A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360224 | |||||||
chr9:68360249 | TAA | T | 3 | a0001c0001t0004g0085 a0003c0008t0026g0234 a0003c0008t0027g0235 |
3 | HG02109.hp1 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.261+2863_261+2864d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68360249 | ||||||
chr9:68360292 | A | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2904A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360292 | |||||||
chr9:68360314 | T | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+2926T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360314 | |||||||
chr9:68360376 | A | C | 4 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(1): Show |
4 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+2988A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360376 | |||||||
chr9:68360388 | T | A | 3 | a0001c0001t0020g0156 a0001c0001t0020g0157 a0002c0009t0016g0246 |
3 | HG00423.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.261+3000T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360388 | |||||||
chr9:68360435 | C | T | 1 | a0001c0004t0002g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.261+3047C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360435 | |||||||
chr9:68360562 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3174C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360562 | |||||||
chr9:68360655 | G | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3267G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360655 | |||||||
chr9:68360709 | C | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3321C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360709 | |||||||
chr9:68360712 | A | G | 2 | a0003c0008t0026g0234 a0003c0008t0027g0235 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.261+3324A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360712 | |||||||
chr9:68360750 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3362G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360750 | |||||||
chr9:68360766 | G | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3378G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360766 | |||||||
chr9:68360796 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3408T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360796 | |||||||
chr9:68360831 | C | T | 4 | a0001c0001t0009g0119 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+3443C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360831 | |||||||
chr9:68360832 | G | A | 3 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0002c0009t0016g0246 |
3 | HG00423.hp2 HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+3444G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360832 | |||||||
chr9:68360834 | AATC | A | 3 | a0001c0004t0002g0242 a0001c0004t0006g0241 a0001c0004t0006g0244 |
3 | HG01891.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.261+3450_261+3452d others(5): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68360834 | ||||||
chr9:68360839 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3451T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360839 | |||||||
chr9:68360862 | G | A | 37 | a0001c0001t0003g0120 a0001c0001t0003g0166 a0001c0001t0003g0170 others(34): Show |
37 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.261+3474G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360862 | |||||||
chr9:68360953 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3565C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68360953 | |||||||
chr9:68361007 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3619T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361007 | |||||||
chr9:68361084 | A | C | 37 | a0001c0001t0003g0120 a0001c0001t0003g0166 a0001c0001t0003g0170 others(34): Show |
37 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.261+3696A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361084 | |||||||
chr9:68361098 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3710G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361098 | |||||||
chr9:68361104 | A | G | 65 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(62): Show |
65 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.261+3716A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361104 | |||||||
chr9:68361116 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3728C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361116 | |||||||
chr9:68361119 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3731C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361119 | |||||||
chr9:68361142 | A | T | 3 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0002c0009t0016g0246 |
3 | HG00423.hp2 HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+3754A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361142 | |||||||
chr9:68361287 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3899C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361287 | |||||||
chr9:68361312 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3924A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361312 | |||||||
chr9:68361331 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3943A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361331 | |||||||
chr9:68361349 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3961C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361349 | |||||||
chr9:68361359 | C | T | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.261+3971C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361359 | |||||||
chr9:68361365 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+3977C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361365 | |||||||
chr9:68361390 | G | A | 13 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(10): Show |
13 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.261+4002G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361390 | |||||||
chr9:68361403 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4015T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361403 | |||||||
chr9:68361667 | G | T | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.261+4279G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361667 | |||||||
chr9:68361686 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4298G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361686 | |||||||
chr9:68361712 | C | T | 3 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0002t0001g0155 |
3 | HG00140.hp1 HG02109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.261+4324C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361712 | |||||||
chr9:68361713 | G | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4325G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361713 | |||||||
chr9:68361790 | G | A | 1 | a0001c0002t0002g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.261+4402G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361790 | |||||||
chr9:68361814 | T | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4426T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361814 | |||||||
chr9:68361876 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4488C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361876 | |||||||
chr9:68361891 | G | T | 47 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(44): Show |
47 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.261+4503G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361891 | |||||||
chr9:68361915 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4527C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361915 | |||||||
chr9:68361922 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4534T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361922 | |||||||
chr9:68361937 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4549T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68361937 | |||||||
chr9:68362020 | T | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4632T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362020 | |||||||
chr9:68362037 | G | A | 2 | a0001c0001t0004g0151 a0001c0001t0014g0094 |
2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.261+4649G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362037 | |||||||
chr9:68362118 | A | C | 86 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0085 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.261+4730A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362118 | |||||||
chr9:68362268 | T | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4880T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362268 | |||||||
chr9:68362275 | T | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+4887T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362275 | |||||||
chr9:68362343 | G | T | 3 | a0001c0001t0007g0232 a0001c0001t0007g0233 a0001c0001t0012g0231 |
3 | HG02055.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.261+4955G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362343 | |||||||
chr9:68362372 | A | G | 9 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+4984A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362372 | |||||||
chr9:68362409 | G | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+5021G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362409 | |||||||
chr9:68362444 | A | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+5056A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362444 | |||||||
chr9:68362523 | A | G | 1 | a0001c0002t0002g0068 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.261+5135A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362523 | |||||||
chr9:68362572 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+5184G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362572 | |||||||
chr9:68362756 | C | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+5368C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362756 | |||||||
chr9:68362778 | G | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+5390G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362778 | |||||||
chr9:68362821 | T | A | 3 | a0001c0001t0004g0151 a0001c0001t0014g0094 a0002c0009t0016g0246 |
3 | HG00423.hp2 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.261+5433T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362821 | |||||||
chr9:68362865 | CT | C | 98 | a0001c0001t0001g0086 a0001c0001t0001g0099 a0001c0001t0002g0005 others(95): Show |
98 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.261+5498delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68362865 | ||||||
chr9:68362865 | CTT | C | 17 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(14): Show |
17 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.261+5497_261+5498d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68362865 | ||||||
chr9:68362872 | T | C | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.261+5484T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362872 | |||||||
chr9:68362918 | G | A | 65 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(62): Show |
65 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.261+5530G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362918 | |||||||
chr9:68362947 | G | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+5559G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362947 | |||||||
chr9:68362954 | C | T | 3 | a0001c0002t0002g0036 a0001c0002t0002g0049 a0001c0002t0002g0066 |
3 | NA18955.hp1 NA18975.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.261+5566C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68362954 | |||||||
chr9:68363025 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+5637C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363025 | |||||||
chr9:68363060 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+5672G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363060 | |||||||
chr9:68363076 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.261+5688G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363076 | |||||||
chr9:68363117 | G | A | 1 | a0001c0003t0005g0007 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.261+5729G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363117 | |||||||
chr9:68363148 | GTGTGAGC others(3): Show |
G | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.261+5763_261+5772d others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68363148 | ||||||
chr9:68363174 | C | T | 1 | a0001c0001t0007g0171 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.261+5786C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363174 | |||||||
chr9:68363237 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.261+5849A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363237 | |||||||
chr9:68363383 | G | A | 2 | a0001c0001t0010g0214 a0001c0001t0011g0215 |
2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.261+5995G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363383 | |||||||
chr9:68363393 | A | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+6005A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363393 | |||||||
chr9:68363416 | C | T | 4 | a0001c0001t0009g0119 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+6028C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363416 | |||||||
chr9:68363430 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+6042C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363430 | |||||||
chr9:68363453 | G | A | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.261+6065G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363453 | |||||||
chr9:68363526 | T | C | 2 | a0001c0001t0001g0100 a0002c0009t0016g0246 |
2 | HG00423.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.261+6138T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363526 | |||||||
chr9:68363898 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+6510C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363898 | |||||||
chr9:68363917 | A | G | 17 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0003t0001g0006 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+6529A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68363917 | |||||||
chr9:68364028 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+6640A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364028 | |||||||
chr9:68364066 | G | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+6678G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364066 | |||||||
chr9:68364117 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+6729A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364117 | |||||||
chr9:68364161 | T | C | 56 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(53): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.261+6773T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364161 | |||||||
chr9:68364162 | G | A | 1 | a0001c0002t0008g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.261+6774G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364162 | |||||||
chr9:68364240 | T | C | 56 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(53): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.261+6852T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364240 | |||||||
chr9:68364272 | T | C | 52 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(49): Show |
52 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.261+6884T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364272 | |||||||
chr9:68364292 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+6904G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364292 | |||||||
chr9:68364293 | C | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+6905C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364293 | |||||||
chr9:68364316 | G | A | 1 | a0001c0005t0014g0088 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.261+6928G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364316 | |||||||
chr9:68364322 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+6934G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364322 | |||||||
chr9:68364323 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+6935C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364323 | |||||||
chr9:68364351 | T | A | 1 | a0001c0001t0003g0196 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+6963T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364351 | |||||||
chr9:68364381 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+6993A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364381 | |||||||
chr9:68364583 | A | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+7195A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364583 | |||||||
chr9:68364590 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+7202G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364590 | |||||||
chr9:68364649 | C | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+7261C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364649 | |||||||
chr9:68364683 | A | T | 56 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(53): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.261+7295A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364683 | |||||||
chr9:68364772 | C | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+7384C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364772 | |||||||
chr9:68364806 | G | A | 4 | a0001c0002t0013g0045 a0001c0002t0013g0046 a0001c0002t0013g0047 others(1): Show |
4 | HG00735.hp1 HG00741.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+7418G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364806 | |||||||
chr9:68364896 | AT | A | 3 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0024 |
3 | HG00099.hp2 HG01258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.261+7513delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68364896 | ||||||
chr9:68364994 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+7606C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68364994 | |||||||
chr9:68365131 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+7743T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365131 | |||||||
chr9:68365161 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+7773C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365161 | |||||||
chr9:68365282 | A | T | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.261+7894A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365282 | |||||||
chr9:68365401 | A | T | 3 | a0001c0001t0001g0150 a0001c0001t0005g0117 a0001c0001t0005g0149 |
3 | HG02129.hp1 NA18952.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.261+8013A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365401 | |||||||
chr9:68365442 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8054T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365442 | |||||||
chr9:68365508 | T | C | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.261+8120T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365508 | |||||||
chr9:68365519 | A | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8131A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365519 | |||||||
chr9:68365564 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8176G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365564 | |||||||
chr9:68365632 | G | A | 17 | a0001c0001t0001g0199 a0001c0001t0002g0070 a0001c0001t0002g0071 others(14): Show |
17 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(14): Show |
intron_variant | MODIFIER | c.261+8244G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365632 | |||||||
chr9:68365636 | A | G | 9 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(6): Show |
9 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+8248A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365636 | |||||||
chr9:68365656 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8268C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365656 | |||||||
chr9:68365691 | A | G | 4 | a0001c0001t0009g0119 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+8303A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365691 | |||||||
chr9:68365705 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8317A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365705 | |||||||
chr9:68365852 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8464G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365852 | |||||||
chr9:68365971 | C | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8583C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365971 | |||||||
chr9:68365973 | G | A | 17 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0003t0001g0006 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+8585G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68365973 | |||||||
chr9:68366160 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.261+8772A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366160 | |||||||
chr9:68366162 | T | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8774T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366162 | |||||||
chr9:68366164 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8776G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366164 | |||||||
chr9:68366286 | G | GA | 5 | a0001c0001t0009g0119 a0001c0005t0009g0208 a0001c0005t0009g0209 others(2): Show |
5 | HG00423.hp2 HG01255.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+8904dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68366286 | ||||||
chr9:68366337 | T | C | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8949T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366337 | |||||||
chr9:68366338 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8950G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366338 | |||||||
chr9:68366367 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8979A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366367 | |||||||
chr9:68366379 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+8991G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366379 | |||||||
chr9:68366448 | C | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+9060C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366448 | |||||||
chr9:68366448 | C | T | 60 | a0001c0001t0004g0085 a0001c0002t0002g0009 a0001c0002t0002g0010 others(57): Show |
60 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.261+9060C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366448 | |||||||
chr9:68366562 | G | A | 1 | a0001c0002t0008g0025 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.261+9174G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366562 | |||||||
chr9:68366591 | C | G | 21 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(18): Show |
21 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.261+9203C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366591 | |||||||
chr9:68366597 | A | T | 123 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(120): Show |
123 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.261+9209A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366597 | |||||||
chr9:68366617 | A | G | 18 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.261+9229A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366617 | |||||||
chr9:68366636 | T | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+9248T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366636 | |||||||
chr9:68366708 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.261+9320A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366708 | |||||||
chr9:68366716 | G | C | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.261+9328G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366716 | |||||||
chr9:68366731 | A | G | 124 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(121): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.261+9343A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366731 | |||||||
chr9:68366817 | A | G | 3 | a0001c0003t0005g0007 a0001c0003t0005g0012 a0001c0003t0005g0013 |
3 | HG00642.hp1 HG01081.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.261+9429A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366817 | |||||||
chr9:68366887 | T | G | 4 | a0001c0001t0009g0119 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+9499T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366887 | |||||||
chr9:68366916 | G | A | 3 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 |
3 | HG03041.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.261+9528G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68366916 | |||||||
chr9:68367060 | T | C | 89 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0085 others(86): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.261+9672T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367060 | |||||||
chr9:68367110 | C | G | 57 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.261+9722C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367110 | |||||||
chr9:68367192 | C | CT | 17 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0003t0001g0006 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+9810dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68367192 | ||||||
chr9:68367230 | G | A | 92 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0085 others(89): Show |
92 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.261+9842G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367230 | |||||||
chr9:68367298 | AC | A | 13 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(10): Show |
13 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.261+9913delC | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68367298 | ||||||
chr9:68367310 | T | C | 89 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0085 others(86): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.261+9922T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367310 | |||||||
chr9:68367378 | T | C | 21 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.261+9990T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367378 | |||||||
chr9:68367494 | T | G | 57 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.261+10106T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367494 | |||||||
chr9:68367591 | A | T | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.261+10203A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367591 | |||||||
chr9:68367690 | C | T | 3 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 |
3 | HG03041.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.261+10302C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367690 | |||||||
chr9:68367719 | A | G | 66 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(63): Show |
66 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.261+10331A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367719 | |||||||
chr9:68367739 | G | A | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.261+10351G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367739 | |||||||
chr9:68367749 | G | A | 4 | a0001c0001t0028g0040 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02559.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+10361G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367749 | |||||||
chr9:68367824 | A | T | 13 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(10): Show |
13 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.262-10375A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367824 | |||||||
chr9:68367892 | T | C | 66 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(63): Show |
66 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.262-10307T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367892 | |||||||
chr9:68367914 | G | C | 10 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-10285G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367914 | |||||||
chr9:68367919 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.262-10280T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367919 | |||||||
chr9:68367920 | G | A | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.262-10279G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367920 | |||||||
chr9:68367952 | T | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.262-10247T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367952 | |||||||
chr9:68367957 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.262-10242G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367957 | |||||||
chr9:68367991 | C | T | 1 | a0001c0004t0024g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.262-10208C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367991 | |||||||
chr9:68367992 | G | A | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.262-10207G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68367992 | |||||||
chr9:68368044 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.262-10155T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68368044 | |||||||
chr9:68368109 | A | C | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-10090A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68368109 | |||||||
chr9:68368324 | A | T | 1 | a0001c0002t0008g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.262-9875A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68368324 | |||||||
chr9:68368418 | C | T | 1 | a0001c0002t0002g0064 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.262-9781C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68368418 | |||||||
chr9:68368587 | T | G | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-9612T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68368587 | |||||||
chr9:68368605 | A | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.262-9594A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68368605 | |||||||
chr9:68368638 | G | GT | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-9551dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68368638 | ||||||
chr9:68368639 | T | G | 57 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.262-9560T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68368639 | |||||||
chr9:68368791 | C | T | 1 | a0001c0002t0002g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.262-9408C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68368791 | |||||||
chr9:68368981 | G | A | 1 | a0001c0005t0004g0089 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.262-9218G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68368981 | |||||||
chr9:68368992 | T | C | 3 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 |
3 | HG03041.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.262-9207T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68368992 | |||||||
chr9:68369272 | G | A | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.262-8927G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369272 | |||||||
chr9:68369456 | A | G | 124 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(121): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.262-8743A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369456 | |||||||
chr9:68369535 | TA | T | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-8663delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369535 | |||||||
chr9:68369537 | C | G | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-8662C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369537 | |||||||
chr9:68369632 | T | A | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.262-8567T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369632 | |||||||
chr9:68369638 | G | A | 3 | a0001c0001t0010g0216 a0001c0001t0010g0217 a0001c0001t0011g0212 |
3 | HG02027.hp1 NA18980.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.262-8561G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369638 | |||||||
chr9:68369798 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.262-8401G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369798 | |||||||
chr9:68369814 | CT | C | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-8383delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68369814 | ||||||
chr9:68369824 | T | G | 4 | a0001c0001t0028g0040 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02559.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-8375T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369824 | |||||||
chr9:68369914 | C | T | 9 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-8285C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369914 | |||||||
chr9:68369984 | A | G | 161 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.262-8215A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369984 | |||||||
chr9:68369991 | T | C | 89 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0085 others(86): Show |
89 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.262-8208T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68369991 | |||||||
chr9:68370054 | G | A | 14 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(11): Show |
14 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.262-8145G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370054 | |||||||
chr9:68370105 | G | A | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.262-8094G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370105 | |||||||
chr9:68370129 | A | G | 124 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(121): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.262-8070A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370129 | |||||||
chr9:68370294 | A | G | 37 | a0001c0001t0003g0120 a0001c0001t0003g0166 a0001c0001t0003g0170 others(34): Show |
37 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.262-7905A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370294 | |||||||
chr9:68370308 | AAG | A | 21 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(18): Show |
21 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.262-7887_262-7886d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68370308 | ||||||
chr9:68370387 | A | G | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.262-7812A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370387 | |||||||
chr9:68370391 | A | G | 53 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(50): Show |
53 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.262-7808A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370391 | |||||||
chr9:68370508 | C | G | 1 | a0001c0005t0009g0210 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.262-7691C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370508 | |||||||
chr9:68370581 | A | C | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.262-7618A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370581 | |||||||
chr9:68370681 | A | C | 3 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 |
3 | HG03041.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.262-7518A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370681 | |||||||
chr9:68370828 | G | A | 68 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(65): Show |
68 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.262-7371G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370828 | |||||||
chr9:68370881 | C | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.262-7318C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370881 | |||||||
chr9:68370885 | G | A | 2 | a0001c0007t0004g0091 a0001c0007t0004g0098 |
2 | HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.262-7314G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68370885 | |||||||
chr9:68371068 | A | G | 17 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0003t0001g0006 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-7131A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371068 | |||||||
chr9:68371154 | T | A | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.262-7045T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371154 | |||||||
chr9:68371161 | C | A | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.262-7038C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371161 | |||||||
chr9:68371379 | C | T | 9 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-6820C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371379 | |||||||
chr9:68371381 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.262-6818G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371381 | |||||||
chr9:68371626 | C | A | 4 | a0001c0002t0013g0045 a0001c0002t0013g0046 a0001c0002t0013g0047 others(1): Show |
4 | HG00735.hp1 HG00741.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-6573C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371626 | |||||||
chr9:68371664 | T | TAG | 87 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0001t0009g0211 others(84): Show |
87 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.262-6534_262-6533d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68371664 | ||||||
chr9:68371731 | T | C | 5 | a0001c0001t0001g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 others(2): Show |
5 | HG02257.hp2 HG03195.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-6468T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371731 | |||||||
chr9:68371736 | A | C | 87 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0001t0009g0211 others(84): Show |
87 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.262-6463A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371736 | |||||||
chr9:68371817 | G | A | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.262-6382G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371817 | |||||||
chr9:68371827 | A | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.262-6372A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371827 | |||||||
chr9:68371870 | CAG | C | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-6326_262-6325d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68371870 | ||||||
chr9:68371958 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.262-6241T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371958 | |||||||
chr9:68371976 | C | T | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.262-6223C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68371976 | |||||||
chr9:68372022 | T | G | 1 | a0001c0001t0003g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.262-6177T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372022 | |||||||
chr9:68372096 | ATACAAAC others(12): Show |
A | 4 | a0001c0001t0004g0154 a0001c0002t0001g0155 a0001c0007t0004g0091 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-6087_262-6069d others(21): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68372096 | ||||||
chr9:68372159 | C | A | 1 | a0001c0002t0002g0014 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.262-6040C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372159 | |||||||
chr9:68372213 | G | A | 57 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.262-5986G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372213 | |||||||
chr9:68372236 | C | T | 4 | a0001c0001t0028g0040 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02559.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-5963C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372236 | |||||||
chr9:68372237 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.262-5962G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372237 | |||||||
chr9:68372280 | C | CT | 110 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0085 others(107): Show |
110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.262-5919_262-5918i others(3): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372280 | |||||||
chr9:68372291 | G | C | 14 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(11): Show |
14 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.262-5908G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372291 | |||||||
chr9:68372397 | G | T | 1 | a0001c0001t0001g0147 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.262-5802G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372397 | |||||||
chr9:68372431 | C | T | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-5768C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372431 | |||||||
chr9:68372442 | A | G | 17 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0003t0001g0006 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-5757A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372442 | |||||||
chr9:68372454 | C | G | 87 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0001t0009g0211 others(84): Show |
87 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.262-5745C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372454 | |||||||
chr9:68372479 | T | C | 21 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(18): Show |
21 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.262-5720T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372479 | |||||||
chr9:68372480 | G | A | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.262-5719G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372480 | |||||||
chr9:68372511 | G | A | 9 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(6): Show |
9 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-5688G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372511 | |||||||
chr9:68372551 | G | A | 1 | a0001c0002t0002g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.262-5648G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372551 | |||||||
chr9:68372603 | C | T | 87 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0001t0009g0211 others(84): Show |
87 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.262-5596C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372603 | |||||||
chr9:68372647 | A | G | 1 | a0003c0008t0027g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.262-5552A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372647 | |||||||
chr9:68372725 | C | T | 2 | a0001c0002t0002g0063 a0001c0002t0002g0064 |
2 | HG01109.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.262-5474C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372725 | |||||||
chr9:68372806 | T | A | 21 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.262-5393T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372806 | |||||||
chr9:68372843 | A | G | 21 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(18): Show |
21 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.262-5356A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372843 | |||||||
chr9:68372904 | C | T | 1 | a0004c0013t0001g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.262-5295C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372904 | |||||||
chr9:68372905 | G | A | 23 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(20): Show |
23 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.262-5294G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372905 | |||||||
chr9:68372929 | T | C | 1 | a0001c0001t0014g0094 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.262-5270T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372929 | |||||||
chr9:68372978 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.262-5221C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68372978 | |||||||
chr9:68373034 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.262-5165C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373034 | |||||||
chr9:68373036 | A | T | 15 | a0001c0001t0003g0170 a0001c0001t0003g0189 a0001c0001t0003g0190 others(12): Show |
15 | HG00099.hp1 HG00642.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.262-5163A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373036 | |||||||
chr9:68373053 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.262-5146C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373053 | |||||||
chr9:68373101 | T | C | 21 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(18): Show |
21 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.262-5098T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373101 | |||||||
chr9:68373131 | T | C | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.262-5068T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373131 | |||||||
chr9:68373162 | T | G | 124 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(121): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.262-5037T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373162 | |||||||
chr9:68373185 | C | A | 124 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(121): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.262-5014C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373185 | |||||||
chr9:68373392 | A | T | 57 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.262-4807A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373392 | |||||||
chr9:68373432 | C | T | 4 | a0001c0001t0028g0040 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02559.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-4767C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373432 | |||||||
chr9:68373437 | T | C | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-4762T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373437 | |||||||
chr9:68373562 | C | T | 21 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.262-4637C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373562 | |||||||
chr9:68373646 | C | A | 66 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(63): Show |
66 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.262-4553C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373646 | |||||||
chr9:68373763 | C | A | 4 | a0001c0001t0028g0040 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02559.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-4436C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373763 | |||||||
chr9:68373865 | C | A | 1 | a0001c0001t0005g0159 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.262-4334C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68373865 | |||||||
chr9:68374042 | G | C | 1 | a0001c0002t0002g0041 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.262-4157G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374042 | |||||||
chr9:68374136 | C | T | 17 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0003t0001g0006 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-4063C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374136 | |||||||
chr9:68374274 | A | G | 17 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0003t0001g0006 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-3925A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374274 | |||||||
chr9:68374290 | G | C | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.262-3909G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374290 | |||||||
chr9:68374333 | A | G | 124 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(121): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.262-3866A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374333 | |||||||
chr9:68374390 | T | C | 53 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(50): Show |
53 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.262-3809T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374390 | |||||||
chr9:68374401 | C | A | 1 | a0001c0001t0007g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.262-3798C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374401 | |||||||
chr9:68374518 | G | A | 1 | a0001c0001t0007g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.262-3681G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374518 | |||||||
chr9:68374683 | A | G | 1 | a0001c0002t0013g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.262-3516A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374683 | |||||||
chr9:68374712 | C | T | 1 | a0001c0001t0010g0228 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.262-3487C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374712 | |||||||
chr9:68374826 | A | T | 3 | a0001c0001t0004g0085 a0003c0008t0026g0234 a0003c0008t0027g0235 |
3 | HG02109.hp1 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.262-3373A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374826 | |||||||
chr9:68374899 | C | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.262-3300C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374899 | |||||||
chr9:68374915 | C | A | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.262-3284C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68374915 | |||||||
chr9:68375231 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.262-2968T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375231 | |||||||
chr9:68375238 | T | C | 4 | a0001c0001t0028g0040 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02559.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-2961T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375238 | |||||||
chr9:68375239 | A | C | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.262-2960A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375239 | |||||||
chr9:68375262 | C | T | 2 | a0001c0001t0003g0195 a0001c0001t0003g0196 |
2 | HG00642.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.262-2937C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375262 | |||||||
chr9:68375263 | G | A | 3 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 |
3 | HG03041.hp1 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.262-2936G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375263 | |||||||
chr9:68375314 | C | T | 13 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(10): Show |
13 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.262-2885C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375314 | |||||||
chr9:68375426 | A | G | 9 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-2773A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375426 | |||||||
chr9:68375480 | C | T | 66 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(63): Show |
66 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.262-2719C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375480 | |||||||
chr9:68375503 | C | T | 1 | a0001c0002t0002g0062 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.262-2696C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375503 | |||||||
chr9:68375606 | G | A | 66 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(63): Show |
66 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.262-2593G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375606 | |||||||
chr9:68375713 | G | A | 66 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(63): Show |
66 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.262-2486G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375713 | |||||||
chr9:68375925 | C | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0173 |
2 | NA18612.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.262-2274C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68375925 | |||||||
chr9:68376129 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.262-2070G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376129 | |||||||
chr9:68376135 | A | G | 1 | a0001c0002t0002g0016 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.262-2064A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376135 | |||||||
chr9:68376160 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.262-2039A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376160 | |||||||
chr9:68376238 | G | A | 2 | a0001c0007t0004g0091 a0001c0007t0004g0098 |
2 | HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.262-1961G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376238 | |||||||
chr9:68376402 | G | A | 21 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.262-1797G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376402 | |||||||
chr9:68376475 | C | CTG | 30 | a0001c0001t0001g0199 a0001c0001t0002g0005 a0001c0001t0003g0166 others(27): Show |
30 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.262-1676_262-1675d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376475 | C | CTGTG | 15 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0003g0191 others(12): Show |
15 | HG00099.hp2 HG01258.hp1 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.262-1678_262-1675d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376475 | C | CTGTGTG | 4 | a0001c0001t0003g0195 a0001c0001t0003g0204 a0001c0002t0002g0064 others(1): Show |
4 | HG01168.hp1 HG01255.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-1680_262-1675d others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376475 | C | CTGTGTGT others(3): Show |
1 | a0001c0002t0002g0036 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.262-1684_262-1675d others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376475 | CTG | C | 54 | a0001c0001t0001g0093 a0001c0001t0001g0099 a0001c0001t0001g0100 others(51): Show |
54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.262-1676_262-1675d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376475 | CTGTG | C | 15 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0139 others(12): Show |
15 | HG01496.hp1 HG02055.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.262-1678_262-1675d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376475 | CTGTGTG | C | 6 | a0001c0001t0001g0142 a0001c0001t0004g0106 a0001c0001t0011g0218 others(3): Show |
6 | HG00280.hp1 HG00741.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.262-1680_262-1675d others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376475 | CTGTGTGT others(1): Show |
C | 28 | a0001c0001t0001g0086 a0001c0001t0001g0121 a0001c0001t0001g0143 others(25): Show |
28 | HG00408.hp1 HG00438.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.262-1682_262-1675d others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376475 | CTGTGTGT others(3): Show |
C | 6 | a0001c0001t0002g0073 a0001c0001t0003g0203 a0001c0001t0004g0085 others(3): Show |
6 | HG01261.hp1 HG02027.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.262-1684_262-1675d others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376475 | CTGTGTGT others(5): Show |
C | 11 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0074 others(8): Show |
11 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.262-1686_262-1675d others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376475 | CTGTGTGT others(7): Show |
C | 3 | a0001c0001t0001g0201 a0001c0001t0002g0070 a0001c0001t0009g0119 |
3 | HG02572.hp1 HG02622.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.262-1688_262-1675d others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376475 | ||||||
chr9:68376524 | T | TG | 4 | a0001c0001t0003g0206 a0001c0002t0002g0041 a0001c0002t0002g0063 others(1): Show |
4 | HG01109.hp1 HG02135.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-1675_262-1674i others(3): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376524 | |||||||
chr9:68376733 | C | T | 1 | a0001c0001t0011g0212 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.262-1466C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376733 | |||||||
chr9:68376765 | A | ATTTC | 22 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0096 others(19): Show |
22 | HG00609.hp2 HG00673.hp2 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.262-1368_262-1365d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376765 | ||||||
chr9:68376765 | A | ATTTCTTT others(1): Show |
4 | a0001c0001t0001g0112 a0001c0001t0002g0080 a0001c0001t0006g0079 others(1): Show |
4 | HG00280.hp2 HG02055.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-1372_262-1365d others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376765 | ||||||
chr9:68376765 | A | ATTTCTTT others(5): Show |
1 | a0001c0001t0005g0161 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.262-1376_262-1365d others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376765 | ||||||
chr9:68376765 | A | ATTTCTTT others(13): Show |
1 | a0001c0001t0001g0128 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.262-1384_262-1365d others(22): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376765 | ||||||
chr9:68376765 | ATTTC | A | 28 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0124 others(25): Show |
28 | HG00140.hp1 HG01258.hp2 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.262-1368_262-1365d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376765 | ||||||
chr9:68376765 | ATTTCTTT others(1): Show |
A | 25 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0143 others(22): Show |
25 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.262-1372_262-1365d others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376765 | ||||||
chr9:68376765 | ATTTCTTT others(5): Show |
A | 11 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0002g0074 others(8): Show |
11 | HG01168.hp1 HG01261.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.262-1376_262-1365d others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376765 | ||||||
chr9:68376765 | ATTTCTTT others(9): Show |
A | 4 | a0001c0001t0001g0102 a0001c0001t0001g0108 a0001c0001t0003g0166 others(1): Show |
4 | HG02922.hp2 HG03225.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.262-1380_262-1365d others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376765 | ||||||
chr9:68376765 | ATTTCTTT others(13): Show |
A | 1 | a0001c0001t0001g0129 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.262-1384_262-1365d others(22): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376765 | ||||||
chr9:68376765 | ATTTCTTT others(29): Show |
A | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-1400_262-1365d others(38): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376765 | ||||||
chr9:68376805 | CTTTCTTT others(3): Show |
C | 1 | a0001c0002t0002g0042 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.262-1392_262-1383d others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376805 | ||||||
chr9:68376813 | C | A | 17 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(14): Show |
17 | HG00408.hp1 HG01261.hp2 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-1386C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376813 | |||||||
chr9:68376815 | T | TTCTTTCT others(3): Show |
3 | a0001c0003t0005g0007 a0001c0003t0005g0012 a0001c0014t0004g0018 |
3 | HG00642.hp1 HG02559.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.262-1382_262-1373d others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376815 | ||||||
chr9:68376819 | T | TTC | 10 | a0001c0001t0006g0008 a0001c0002t0002g0032 a0001c0002t0002g0057 others(7): Show |
10 | HG00639.hp2 HG01071.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-1378_262-1377d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376819 | ||||||
chr9:68376823 | T | TTC | 19 | a0001c0001t0002g0005 a0001c0002t0002g0003 a0001c0002t0002g0004 others(16): Show |
19 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.262-1374_262-1373d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376823 | ||||||
chr9:68376825 | C | G | 1 | a0003c0008t0027g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.262-1374C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376825 | |||||||
chr9:68376825 | CTTTCTTT others(5): Show |
C | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.262-1372_262-1361d others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376825 | ||||||
chr9:68376831 | T | C | 12 | a0001c0002t0002g0016 a0001c0002t0002g0026 a0001c0002t0002g0038 others(9): Show |
12 | HG00323.hp2 HG00408.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.262-1368T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376831 | |||||||
chr9:68376832 | TC | T | 6 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0002t0002g0041 others(3): Show |
6 | HG01891.hp1 HG02129.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-1366delC | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376832 | |||||||
chr9:68376833 | C | T | 13 | a0001c0002t0002g0016 a0001c0002t0002g0026 a0001c0002t0002g0038 others(10): Show |
13 | HG00323.hp2 HG00408.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.262-1366C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376833 | |||||||
chr9:68376834 | T | TTTC | 25 | a0001c0001t0002g0005 a0001c0002t0002g0003 a0001c0002t0002g0004 others(22): Show |
25 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.262-1365_262-1364i others(5): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376834 | |||||||
chr9:68376834 | T | TTTCTCTT others(19): Show |
1 | a0001c0003t0001g0011 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.262-1365_262-1364i others(28): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376834 | |||||||
chr9:68376834 | T | TTTCTCTT others(10): Show |
7 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0035 others(4): Show |
7 | HG00438.hp1 HG00738.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-1365_262-1364i others(19): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376834 | |||||||
chr9:68376834 | T | TTTCTCTT others(14): Show |
1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.262-1365_262-1364i others(23): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376834 | |||||||
chr9:68376834 | T | TTTCTCTT others(18): Show |
2 | a0001c0003t0001g0006 a0001c0003t0001g0019 |
2 | NA18992.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.262-1365_262-1364i others(27): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376834 | |||||||
chr9:68376834 | T | TTTCTTTC others(14): Show |
2 | a0001c0002t0002g0049 a0001c0002t0002g0068 |
2 | NA18955.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.262-1365_262-1364i others(23): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376834 | |||||||
chr9:68376834 | T | TTTCTTTC others(22): Show |
1 | a0003c0008t0027g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.262-1365_262-1364i others(31): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376834 | |||||||
chr9:68376834 | TC | T | 13 | a0001c0001t0001g0086 a0001c0001t0006g0008 a0001c0002t0002g0015 others(10): Show |
13 | HG00639.hp2 HG01071.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.262-1364delC | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376834 | |||||||
chr9:68376835 | C | CTTTCTTT others(2): Show |
8 | a0001c0002t0002g0016 a0001c0002t0002g0026 a0001c0002t0002g0038 others(5): Show |
8 | HG00408.hp2 HG00735.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.262-1361_262-1353d others(11): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376835 | ||||||
chr9:68376835 | C | CTTTCTTT others(6): Show |
16 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(13): Show |
16 | HG00741.hp2 HG01106.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.262-1361_262-1349d others(15): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376835 | ||||||
chr9:68376835 | C | CTTTCTTT others(10): Show |
5 | a0001c0001t0004g0085 a0001c0003t0001g0017 a0001c0003t0005g0013 others(2): Show |
5 | HG00323.hp2 HG01081.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-1363_262-1347d others(19): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376835 | ||||||
chr9:68376835 | C | CTTTCTTT others(14): Show |
1 | a0001c0017t0004g0069 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.262-1347_262-1346i others(23): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376835 | ||||||
chr9:68376835 | C | T | 39 | a0001c0001t0002g0005 a0001c0001t0028g0040 a0001c0002t0002g0003 others(36): Show |
39 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.262-1364C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376835 | |||||||
chr9:68376849 | T | C | 6 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0002t0002g0041 others(3): Show |
6 | HG01891.hp1 HG02129.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-1350T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376849 | |||||||
chr9:68376851 | C | T | 8 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0002t0002g0041 others(5): Show |
8 | HG01891.hp1 HG02129.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.262-1348C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376851 | |||||||
chr9:68376853 | C | T | 2 | a0001c0003t0009g0230 a0001c0005t0009g0210 |
2 | HG01255.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.262-1346C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376853 | |||||||
chr9:68376855 | T | C | 1 | a0001c0005t0009g0210 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.262-1344T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376855 | |||||||
chr9:68376861 | C | T | 13 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0001t0019g0001 others(10): Show |
13 | HG01891.hp1 HG02129.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.262-1338C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376861 | |||||||
chr9:68376864 | T | C | 13 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0001t0019g0001 others(10): Show |
13 | HG01891.hp1 HG02129.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.262-1335T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376864 | |||||||
chr9:68376874 | C | T | 76 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.262-1325C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376874 | |||||||
chr9:68376876 | T | C | 74 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(71): Show |
74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.262-1323T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376876 | |||||||
chr9:68376886 | T | C | 57 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.262-1313T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376886 | |||||||
chr9:68376886 | TTTTC | T | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.262-1303_262-1300d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376886 | ||||||
chr9:68376890 | C | T | 55 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(52): Show |
55 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.262-1309C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376890 | |||||||
chr9:68376894 | C | T | 2 | a0001c0005t0004g0089 a0001c0005t0014g0088 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.262-1305C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376894 | |||||||
chr9:68376896 | T | C | 37 | a0001c0001t0003g0120 a0001c0001t0003g0166 a0001c0001t0003g0170 others(34): Show |
37 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.262-1303T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376896 | |||||||
chr9:68376900 | C | T | 57 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.262-1299C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376900 | |||||||
chr9:68376902 | CTCTT | C | 28 | a0001c0001t0002g0005 a0001c0001t0004g0085 a0001c0001t0006g0008 others(25): Show |
28 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.262-1283_262-1280d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68376902 | ||||||
chr9:68376904 | C | T | 2 | a0001c0005t0004g0089 a0001c0005t0014g0088 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.262-1295C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376904 | |||||||
chr9:68376906 | T | C | 57 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.262-1293T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376906 | |||||||
chr9:68376943 | C | T | 24 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(21): Show |
24 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.262-1256C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68376943 | |||||||
chr9:68377055 | T | A | 4 | a0001c0001t0028g0040 a0001c0005t0009g0208 a0001c0005t0009g0209 others(1): Show |
4 | HG01255.hp2 HG02559.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-1144T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377055 | |||||||
chr9:68377072 | G | A | 1 | a0001c0002t0013g0046 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.262-1127G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377072 | |||||||
chr9:68377077 | C | A | 1 | a0001c0001t0010g0214 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.262-1122C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377077 | |||||||
chr9:68377175 | C | T | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.262-1024C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377175 | |||||||
chr9:68377180 | G | A | 21 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.262-1019G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377180 | |||||||
chr9:68377209 | A | C | 5 | a0001c0001t0001g0086 a0001c0005t0004g0089 a0001c0005t0014g0087 others(2): Show |
5 | HG02647.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-990A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377209 | |||||||
chr9:68377414 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.262-785G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377414 | |||||||
chr9:68377495 | A | G | 21 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0001t0028g0040 others(18): Show |
21 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.262-704A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377495 | |||||||
chr9:68377584 | C | T | 33 | a0001c0001t0003g0120 a0001c0001t0003g0166 a0001c0001t0003g0170 others(30): Show |
33 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.262-615C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377584 | |||||||
chr9:68377592 | A | G | 92 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0085 others(89): Show |
92 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.262-607A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377592 | |||||||
chr9:68377891 | T | C | 53 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0014 others(50): Show |
53 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.262-308T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377891 | |||||||
chr9:68377909 | C | G | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.262-290C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68377909 | |||||||
chr9:68378044 | C | T | 4 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0002t0002g0003 others(1): Show |
4 | HG02258.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-155C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68378044 | |||||||
chr9:68378104 | T | G | 161 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.262-95T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68378104 | |||||||
chr9:68378165 | G | C | 92 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0085 others(89): Show |
92 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.262-34G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | chr9 | 68378165 | |||||||
chr9:68378176 | A | AT | 82 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0085 others(79): Show |
82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.262-12dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 68378176 | ||||||
chr9:68378589 | G | A | 124 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(121): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.424+228G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68378589 | |||||||
chr9:68378650 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.424+289C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68378650 | |||||||
chr9:68378685 | T | A | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.424+324T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68378685 | |||||||
chr9:68378776 | C | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.424+415C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68378776 | |||||||
chr9:68378845 | C | T | 1 | a0001c0001t0007g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.424+484C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68378845 | |||||||
chr9:68378852 | C | T | 14 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(11): Show |
14 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.424+491C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68378852 | |||||||
chr9:68379104 | C | T | 2 | a0001c0002t0002g0041 a0001c0002t0002g0042 |
2 | HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.424+743C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68379104 | |||||||
chr9:68379105 | A | G | 2 | a0001c0002t0002g0041 a0001c0002t0002g0042 |
2 | HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.424+744A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68379105 | |||||||
chr9:68379175 | A | G | 3 | a0001c0001t0007g0232 a0001c0001t0007g0233 a0001c0001t0012g0231 |
3 | HG02055.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.424+814A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68379175 | |||||||
chr9:68379304 | A | G | 17 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0003t0001g0006 others(14): Show |
17 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+943A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68379304 | |||||||
chr9:68379421 | G | A | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+1060G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68379421 | |||||||
chr9:68379763 | A | G | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+1402A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68379763 | |||||||
chr9:68379809 | A | T | 10 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+1448A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68379809 | |||||||
chr9:68380088 | A | G | 67 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.424+1727A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380088 | |||||||
chr9:68380112 | A | G | 61 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(58): Show |
61 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.424+1751A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380112 | |||||||
chr9:68380142 | T | C | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+1781T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380142 | |||||||
chr9:68380370 | C | G | 5 | a0001c0001t0001g0143 a0001c0001t0003g0172 a0001c0003t0009g0229 others(2): Show |
5 | HG00438.hp2 HG02647.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+2009C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380370 | |||||||
chr9:68380388 | C | T | 4 | a0001c0001t0003g0172 a0001c0003t0009g0229 a0001c0003t0009g0230 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+2027C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380388 | |||||||
chr9:68380438 | C | T | 4 | a0001c0001t0001g0150 a0001c0001t0005g0117 a0001c0001t0005g0130 others(1): Show |
4 | HG02129.hp1 NA18952.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+2077C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380438 | |||||||
chr9:68380439 | G | A | 4 | a0001c0001t0003g0172 a0001c0003t0009g0229 a0001c0003t0009g0230 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+2078G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380439 | |||||||
chr9:68380548 | A | G | 1 | a0001c0002t0002g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.424+2187A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380548 | |||||||
chr9:68380618 | G | A | 10 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+2257G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380618 | |||||||
chr9:68380704 | T | C | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.424+2343T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380704 | |||||||
chr9:68380717 | C | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+2356C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380717 | |||||||
chr9:68380972 | A | G | 1 | a0001c0002t0002g0052 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.424+2611A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380972 | |||||||
chr9:68380976 | G | A | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.424+2615G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68380976 | |||||||
chr9:68381080 | T | C | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.424+2719T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381080 | |||||||
chr9:68381084 | T | G | 41 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(38): Show |
41 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.424+2723T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381084 | |||||||
chr9:68381088 | C | T | 1 | a0001c0001t0005g0135 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.424+2727C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381088 | |||||||
chr9:68381313 | A | T | 1 | a0001c0001t0003g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.424+2952A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381313 | |||||||
chr9:68381322 | CA | C | 67 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.424+2962delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381322 | |||||||
chr9:68381424 | A | C | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.425-2974A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381424 | |||||||
chr9:68381426 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.425-2972T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381426 | |||||||
chr9:68381443 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.425-2955C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381443 | |||||||
chr9:68381632 | C | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.425-2766C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381632 | |||||||
chr9:68381633 | T | TACAC | 9 | a0001c0002t0001g0155 a0001c0004t0002g0238 a0001c0004t0002g0242 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-2763_425-2760d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68381633 | ||||||
chr9:68381639 | T | C | 67 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.425-2759T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381639 | |||||||
chr9:68381640 | G | A | 67 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.425-2758G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381640 | |||||||
chr9:68381640 | G | GCA | 34 | a0001c0001t0004g0085 a0001c0001t0009g0211 a0001c0001t0010g0214 others(31): Show |
34 | HG00323.hp2 HG00408.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.425-2739_425-2738d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68381640 | ||||||
chr9:68381640 | G | GCACA | 24 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(21): Show |
24 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.425-2741_425-2738d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68381640 | ||||||
chr9:68381661 | A | C | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.425-2737A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381661 | |||||||
chr9:68381851 | T | C | 1 | a0001c0001t0014g0094 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.425-2547T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381851 | |||||||
chr9:68381944 | A | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0173 |
2 | NA18612.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.425-2454A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381944 | |||||||
chr9:68381985 | C | A | 36 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(33): Show |
36 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.425-2413C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68381985 | |||||||
chr9:68382013 | C | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.425-2385C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68382013 | |||||||
chr9:68382030 | A | G | 5 | a0001c0001t0001g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 others(2): Show |
5 | HG02257.hp2 HG03195.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-2368A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68382030 | |||||||
chr9:68382048 | G | T | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.425-2350G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68382048 | |||||||
chr9:68382056 | A | C | 2 | a0001c0001t0005g0159 a0001c0001t0005g0161 |
2 | NA19009.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.425-2342A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68382056 | |||||||
chr9:68382074 | G | A | 5 | a0001c0001t0001g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 others(2): Show |
5 | HG02257.hp2 HG03195.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-2324G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68382074 | |||||||
chr9:68382077 | G | GA | 17 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0002g0071 others(14): Show |
17 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.425-2313dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68382077 | ||||||
chr9:68382101 | C | T | 4 | a0001c0001t0001g0121 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG00438.hp2 NA18941.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-2297C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68382101 | |||||||
chr9:68382235 | A | AT | 16 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0002g0071 others(13): Show |
16 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.425-2159dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68382235 | ||||||
chr9:68382506 | A | G | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.425-1892A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68382506 | |||||||
chr9:68382524 | C | T | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.425-1874C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68382524 | |||||||
chr9:68382569 | G | A | 2 | a0003c0008t0026g0234 a0003c0008t0027g0235 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.425-1829G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68382569 | |||||||
chr9:68382695 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.425-1703T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68382695 | |||||||
chr9:68383084 | G | A | 10 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-1314G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68383084 | |||||||
chr9:68383173 | C | T | 67 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.425-1225C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68383173 | |||||||
chr9:68383268 | A | G | 3 | a0001c0001t0004g0085 a0003c0008t0026g0234 a0003c0008t0027g0235 |
3 | HG02109.hp1 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.425-1130A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68383268 | |||||||
chr9:68383388 | A | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.425-1010A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68383388 | |||||||
chr9:68383400 | G | A | 16 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0002g0071 others(13): Show |
16 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.425-998G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68383400 | |||||||
chr9:68383430 | TG | T | 16 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0002g0071 others(13): Show |
16 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.425-966delG | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68383430 | ||||||
chr9:68383511 | T | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.425-887T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68383511 | |||||||
chr9:68383666 | T | A | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-732T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68383666 | |||||||
chr9:68383694 | C | CA | 60 | a0001c0001t0001g0176 a0001c0001t0003g0192 a0001c0001t0015g0097 others(57): Show |
60 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.425-690dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68383694 | ||||||
chr9:68383694 | C | CAA | 11 | a0001c0001t0011g0215 a0001c0002t0002g0003 a0001c0002t0002g0004 others(8): Show |
11 | HG01175.hp1 HG01891.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.425-691_425-690dup others(2): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68383694 | ||||||
chr9:68383694 | C | CAAA | 16 | a0001c0001t0010g0214 a0001c0001t0010g0216 a0001c0001t0010g0217 others(13): Show |
16 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.425-692_425-690dup others(3): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68383694 | ||||||
chr9:68383694 | CA | C | 9 | a0001c0001t0001g0115 a0001c0001t0004g0151 a0001c0001t0007g0171 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-690delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68383694 | ||||||
chr9:68383740 | TAA | T | 135 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0096 others(132): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.425-638_425-637del others(2): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68383740 | ||||||
chr9:68383740 | TAAA | T | 88 | a0001c0001t0001g0144 a0001c0001t0002g0070 a0001c0001t0006g0076 others(85): Show |
88 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.425-639_425-637del others(3): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68383740 | ||||||
chr9:68383740 | TAAAA | T | 14 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0003t0001g0006 others(11): Show |
14 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.425-640_425-637del others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 68383740 | ||||||
chr9:68383762 | G | C | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.425-636G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68383762 | |||||||
chr9:68383777 | G | A | 34 | a0001c0001t0003g0120 a0001c0001t0003g0166 a0001c0001t0003g0170 others(31): Show |
34 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.425-621G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68383777 | |||||||
chr9:68384051 | C | G | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.425-347C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68384051 | |||||||
chr9:68384086 | C | T | 59 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(56): Show |
59 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.425-312C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68384086 | |||||||
chr9:68384087 | G | A | 1 | a0001c0001t0010g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.425-311G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68384087 | |||||||
chr9:68384190 | A | G | 59 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(56): Show |
59 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.425-208A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68384190 | |||||||
chr9:68384200 | G | C | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.425-198G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68384200 | |||||||
chr9:68384225 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.425-173T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68384225 | |||||||
chr9:68384242 | A | G | 2 | a0001c0001t0002g0070 a0001c0001t0009g0119 |
2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.425-156A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68384242 | |||||||
chr9:68384269 | G | A | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.425-129G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 2/10 | chr9 | 68384269 | |||||||
chr9:68384758 | A | G | 1 | a0001c0004t0025g0236 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.571+214A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68384758 | |||||||
chr9:68384789 | G | A | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.571+245G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68384789 | |||||||
chr9:68384870 | G | A | 2 | a0001c0003t0005g0007 a0001c0003t0005g0012 |
2 | HG00642.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.571+326G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68384870 | |||||||
chr9:68384888 | C | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.571+344C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68384888 | |||||||
chr9:68384946 | C | T | 18 | a0001c0001t0009g0211 a0001c0001t0010g0214 a0001c0001t0010g0216 others(15): Show |
18 | HG00408.hp1 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.571+402C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68384946 | |||||||
chr9:68385143 | A | G | 1 | a0001c0002t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.571+599A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68385143 | |||||||
chr9:68385171 | T | G | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.571+627T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68385171 | |||||||
chr9:68385225 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.571+681A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68385225 | |||||||
chr9:68385230 | T | TACA | 37 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(34): Show |
37 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.571+687_571+689dup others(3): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 68385230 | ||||||
chr9:68385274 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.571+730G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68385274 | |||||||
chr9:68385312 | T | C | 2 | a0001c0001t0017g0221 a0001c0001t0017g0222 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.571+768T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68385312 | |||||||
chr9:68385385 | C | G | 67 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.571+841C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68385385 | |||||||
chr9:68385420 | A | G | 67 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(64): Show |
67 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.571+876A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68385420 | |||||||
chr9:68385629 | T | C | 106 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(103): Show |
106 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.571+1085T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68385629 | |||||||
chr9:68385903 | T | C | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.571+1359T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68385903 | |||||||
chr9:68385941 | T | C | 18 | a0001c0001t0001g0086 a0001c0001t0004g0085 a0001c0003t0001g0006 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.571+1397T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68385941 | |||||||
chr9:68386005 | A | G | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.572-1458A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386005 | |||||||
chr9:68386009 | C | A | 34 | a0001c0001t0003g0120 a0001c0001t0003g0166 a0001c0001t0003g0170 others(31): Show |
34 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.572-1454C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386009 | |||||||
chr9:68386172 | A | C | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.572-1291A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386172 | |||||||
chr9:68386178 | T | C | 1 | a0001c0001t0003g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.572-1285T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386178 | |||||||
chr9:68386202 | A | T | 1 | a0001c0001t0003g0205 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.572-1261A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386202 | |||||||
chr9:68386248 | G | A | 2 | a0003c0008t0026g0234 a0003c0008t0027g0235 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.572-1215G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386248 | |||||||
chr9:68386249 | T | C | 34 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(31): Show |
34 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.572-1214T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386249 | |||||||
chr9:68386262 | A | C | 16 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0002g0071 others(13): Show |
16 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.572-1201A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386262 | |||||||
chr9:68386288 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.572-1175T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386288 | |||||||
chr9:68386398 | A | G | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.572-1065A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386398 | |||||||
chr9:68386581 | T | C | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.572-882T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386581 | |||||||
chr9:68386607 | G | A | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.572-856G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386607 | |||||||
chr9:68386629 | G | A | 2 | a0001c0001t0010g0223 a0001c0001t0010g0228 |
2 | NA18961.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.572-834G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386629 | |||||||
chr9:68386657 | A | G | 1 | a0001c0001t0021g0134 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.572-806A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386657 | |||||||
chr9:68386993 | T | A | 161 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.572-470T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68386993 | |||||||
chr9:68387110 | C | G | 1 | a0001c0002t0013g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.572-353C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68387110 | |||||||
chr9:68387147 | A | G | 69 | a0001c0002t0001g0155 a0001c0002t0002g0003 a0001c0002t0002g0004 others(66): Show |
69 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.572-316A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68387147 | |||||||
chr9:68387222 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.572-241G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68387222 | |||||||
chr9:68387231 | A | G | 2 | a0003c0008t0026g0234 a0003c0008t0027g0235 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.572-232A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68387231 | |||||||
chr9:68387287 | G | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.572-176G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68387287 | |||||||
chr9:68387447 | G | A | 3 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0016t0022g0084 |
3 | HG02647.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.572-16G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 3/10 | chr9 | 68387447 | |||||||
chr9:68387616 | T | G | 8 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0002t0002g0003 others(5): Show |
8 | HG01891.hp1 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.697+28T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68387616 | |||||||
chr9:68387638 | G | C | 33 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0002g0071 others(30): Show |
33 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(30): Show |
intron_variant | MODIFIER | c.697+50G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68387638 | |||||||
chr9:68387702 | G | C | 1 | a0001c0002t0008g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.697+114G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68387702 | |||||||
chr9:68387732 | A | G | 1 | a0001c0002t0013g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.697+144A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68387732 | |||||||
chr9:68387768 | T | C | 1 | a0001c0001t0006g0079 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.697+180T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68387768 | |||||||
chr9:68387834 | G | A | 1 | a0001c0006t0004g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.697+246G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68387834 | |||||||
chr9:68387905 | C | A | 2 | a0001c0007t0004g0091 a0001c0007t0004g0098 |
2 | HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.697+317C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68387905 | |||||||
chr9:68387964 | C | A | 2 | a0001c0003t0005g0012 a0001c0007t0004g0091 |
2 | HG02809.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.697+376C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68387964 | |||||||
chr9:68387981 | CT | C | 3 | a0001c0003t0005g0012 a0001c0007t0004g0091 a0001c0020t0030g0090 |
3 | HG02622.hp1 HG02809.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.697+399delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 68387981 | ||||||
chr9:68387993 | T | C | 4 | a0001c0005t0009g0208 a0001c0005t0009g0209 a0001c0005t0009g0210 others(1): Show |
4 | HG01255.hp2 HG02895.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+405T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68387993 | |||||||
chr9:68388037 | G | A | 129 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0121 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.697+449G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68388037 | |||||||
chr9:68388203 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.697+615A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68388203 | |||||||
chr9:68388235 | G | A | 1 | a0001c0001t0021g0134 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.697+647G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68388235 | |||||||
chr9:68388352 | T | C | 7 | a0001c0001t0001g0086 a0001c0001t0028g0040 a0001c0002t0002g0003 others(4): Show |
7 | HG01255.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.697+764T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68388352 | |||||||
chr9:68388369 | G | C | 53 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(50): Show |
53 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.697+781G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68388369 | |||||||
chr9:68388577 | A | G | 9 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0070 others(6): Show |
9 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.697+989A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68388577 | |||||||
chr9:68388602 | A | G | 1 | a0004c0013t0001g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.697+1014A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68388602 | |||||||
chr9:68388755 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.697+1167G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68388755 | |||||||
chr9:68388899 | CTATCTT | C | 35 | a0001c0001t0001g0110 a0001c0001t0001g0124 a0001c0001t0001g0142 others(32): Show |
35 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.697+1315_697+1320d others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 68388899 | ||||||
chr9:68389058 | G | A | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.697+1470G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389058 | |||||||
chr9:68389133 | A | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+1545A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389133 | |||||||
chr9:68389177 | G | T | 57 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(54): Show |
57 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.697+1589G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389177 | |||||||
chr9:68389186 | T | C | 1 | a0001c0005t0004g0089 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.697+1598T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389186 | |||||||
chr9:68389297 | T | G | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.697+1709T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389297 | |||||||
chr9:68389548 | T | A | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.697+1960T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389548 | |||||||
chr9:68389643 | A | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-1891A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389643 | |||||||
chr9:68389667 | C | A | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.698-1867C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389667 | |||||||
chr9:68389689 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.698-1845A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389689 | |||||||
chr9:68389805 | A | G | 1 | a0001c0001t0007g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.698-1729A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389805 | |||||||
chr9:68389842 | C | T | 3 | a0001c0001t0001g0086 a0001c0002t0002g0003 a0001c0002t0002g0004 |
3 | HG02723.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.698-1692C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389842 | |||||||
chr9:68389979 | A | T | 4 | a0001c0005t0009g0208 a0001c0005t0009g0209 a0001c0005t0009g0210 others(1): Show |
4 | HG01255.hp2 HG02559.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-1555A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68389979 | |||||||
chr9:68390224 | T | C | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.698-1310T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68390224 | |||||||
chr9:68390399 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-1135G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68390399 | |||||||
chr9:68390414 | A | C | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.698-1120A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68390414 | |||||||
chr9:68390426 | C | T | 2 | a0001c0004t0002g0238 a0001c0004t0002g0243 |
2 | HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.698-1108C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68390426 | |||||||
chr9:68390502 | C | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-1032C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68390502 | |||||||
chr9:68390683 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.698-851C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68390683 | |||||||
chr9:68390807 | G | GA | 62 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(59): Show |
62 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.698-725dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 68390807 | ||||||
chr9:68390965 | C | T | 1 | a0001c0002t0013g0046 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.698-569C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68390965 | |||||||
chr9:68391152 | C | A | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.698-382C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68391152 | |||||||
chr9:68391202 | A | G | 153 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.698-332A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68391202 | |||||||
chr9:68391227 | A | G | 153 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.698-307A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68391227 | |||||||
chr9:68391273 | A | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-261A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68391273 | |||||||
chr9:68391428 | G | A | 153 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.698-106G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68391428 | |||||||
chr9:68391461 | G | C | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.698-73G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 4/10 | chr9 | 68391461 | |||||||
chr9:68391878 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.888+154G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 5/10 | chr9 | 68391878 | |||||||
chr9:68391922 | C | T | 2 | a0001c0001t0004g0085 a0001c0001t0028g0040 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.888+198C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 5/10 | chr9 | 68391922 | |||||||
chr9:68392170 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.889-149C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 5/10 | chr9 | 68392170 | |||||||
chr9:68392237 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.889-82G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 5/10 | chr9 | 68392237 | |||||||
chr9:68392522 | T | C | 71 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(68): Show |
71 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.1043+49T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68392522 | |||||||
chr9:68392547 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1043+74C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68392547 | |||||||
chr9:68392573 | G | T | 5 | a0001c0001t0007g0188 a0001c0002t0001g0155 a0001c0007t0004g0091 others(2): Show |
5 | HG02109.hp2 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+100G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68392573 | |||||||
chr9:68392578 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+105C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68392578 | |||||||
chr9:68392729 | G | A | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1043+256G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68392729 | |||||||
chr9:68392932 | A | G | 60 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(57): Show |
60 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1043+459A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68392932 | |||||||
chr9:68393192 | A | T | 34 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(31): Show |
34 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1043+719A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393192 | |||||||
chr9:68393213 | G | A | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1043+740G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393213 | |||||||
chr9:68393300 | T | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+827T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393300 | |||||||
chr9:68393467 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1043+994C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393467 | |||||||
chr9:68393471 | C | T | 60 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(57): Show |
60 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1043+998C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393471 | |||||||
chr9:68393472 | G | A | 1 | a0003c0008t0027g0235 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1043+999G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393472 | |||||||
chr9:68393499 | G | A | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1043+1026G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393499 | |||||||
chr9:68393558 | T | C | 242 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1043+1085T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393558 | |||||||
chr9:68393563 | G | A | 1 | a0001c0001t0014g0094 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1043+1090G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393563 | |||||||
chr9:68393641 | T | C | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+1168T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393641 | |||||||
chr9:68393877 | G | C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+1404G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393877 | |||||||
chr9:68393883 | G | C | 1 | a0001c0002t0002g0068 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1043+1410G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393883 | |||||||
chr9:68393919 | A | C | 58 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(55): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1043+1446A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393919 | |||||||
chr9:68393957 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+1484G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393957 | |||||||
chr9:68393990 | T | C | 1 | a0001c0002t0002g0026 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1043+1517T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68393990 | |||||||
chr9:68394040 | T | C | 2 | a0001c0001t0004g0085 a0001c0001t0028g0040 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1043+1567T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394040 | |||||||
chr9:68394121 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+1648C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394121 | |||||||
chr9:68394265 | A | G | 1 | a0001c0001t0003g0204 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1043+1792A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394265 | |||||||
chr9:68394335 | C | T | 5 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 others(2): Show |
5 | HG02109.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+1862C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394335 | |||||||
chr9:68394344 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+1871G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394344 | |||||||
chr9:68394490 | A | C | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+2017A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394490 | |||||||
chr9:68394647 | G | T | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043+2174G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394647 | |||||||
chr9:68394675 | C | A | 1 | a0001c0002t0002g0026 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1043+2202C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394675 | |||||||
chr9:68394723 | C | A | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1043+2250C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394723 | |||||||
chr9:68394732 | C | T | 1 | a0001c0017t0004g0069 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1043+2259C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394732 | |||||||
chr9:68394768 | G | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+2295G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394768 | |||||||
chr9:68394791 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+2318A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394791 | |||||||
chr9:68394869 | G | A | 3 | a0001c0002t0002g0036 a0001c0002t0002g0049 a0001c0002t0002g0066 |
3 | NA18955.hp1 NA18975.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1043+2396G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394869 | |||||||
chr9:68394875 | G | A | 3 | a0001c0001t0006g0075 a0001c0001t0006g0076 a0001c0001t0006g0079 |
3 | HG00280.hp2 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1043+2402G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394875 | |||||||
chr9:68394915 | C | A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0085 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+2442C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68394915 | |||||||
chr9:68395030 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1043+2557C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68395030 | |||||||
chr9:68395056 | T | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0200 a0001c0001t0004g0138 |
3 | HG01496.hp1 HG03098.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1043+2583T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68395056 | |||||||
chr9:68395163 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0132 a0001c0001t0001g0140 |
3 | HG02135.hp1 NA18965.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1043+2690G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68395163 | |||||||
chr9:68395176 | G | A | 6 | a0001c0001t0010g0220 a0001c0001t0010g0224 a0001c0001t0012g0118 others(3): Show |
6 | HG02698.hp2 HG03490.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1043+2703G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68395176 | |||||||
chr9:68395205 | G | A | 1 | a0001c0002t0008g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1043+2732G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68395205 | |||||||
chr9:68395371 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+2898G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68395371 | |||||||
chr9:68395384 | T | C | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+2911T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68395384 | |||||||
chr9:68395577 | G | A | 90 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1043+3104G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68395577 | |||||||
chr9:68395707 | T | G | 6 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0085 others(3): Show |
6 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043+3234T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68395707 | |||||||
chr9:68395961 | T | TA | 5 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+3500dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68395961 | ||||||
chr9:68396187 | G | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+3714G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68396187 | |||||||
chr9:68396297 | G | T | 1 | a0001c0002t0002g0057 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1043+3824G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68396297 | |||||||
chr9:68396402 | A | C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+3929A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68396402 | |||||||
chr9:68396440 | T | C | 4 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0002t0002g0003 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+3967T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68396440 | |||||||
chr9:68396530 | C | G | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1043+4057C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68396530 | |||||||
chr9:68396949 | C | T | 2 | a0001c0002t0008g0034 a0002c0009t0016g0246 |
2 | HG00423.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1043+4476C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68396949 | |||||||
chr9:68397007 | C | T | 1 | a0001c0002t0002g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1043+4534C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397007 | |||||||
chr9:68397041 | T | G | 74 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1043+4568T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397041 | |||||||
chr9:68397044 | T | A | 6 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0085 others(3): Show |
6 | HG02258.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043+4571T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397044 | |||||||
chr9:68397068 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1043+4595C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397068 | |||||||
chr9:68397252 | C | T | 5 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 others(2): Show |
5 | HG02109.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+4779C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397252 | |||||||
chr9:68397312 | C | T | 4 | a0001c0002t0002g0010 a0001c0002t0002g0014 a0001c0002t0002g0055 others(1): Show |
4 | NA18946.hp2 NA18963.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+4839C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397312 | |||||||
chr9:68397335 | G | A | 1 | a0001c0001t0004g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1043+4862G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397335 | |||||||
chr9:68397367 | G | A | 1 | a0001c0019t0006g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1043+4894G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397367 | |||||||
chr9:68397376 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1043+4903C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397376 | |||||||
chr9:68397427 | A | G | 1 | a0001c0005t0009g0210 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1043+4954A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397427 | |||||||
chr9:68397496 | A | G | 2 | a0001c0002t0002g0063 a0001c0002t0002g0064 |
2 | HG01109.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1043+5023A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397496 | |||||||
chr9:68397649 | G | A | 3 | a0001c0002t0002g0036 a0001c0002t0002g0049 a0001c0002t0002g0066 |
3 | NA18955.hp1 NA18975.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1043+5176G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397649 | |||||||
chr9:68397815 | T | C | 3 | a0001c0005t0009g0208 a0001c0005t0009g0209 a0001c0005t0009g0210 |
3 | HG01255.hp2 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1043+5342T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397815 | |||||||
chr9:68397976 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+5503G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68397976 | |||||||
chr9:68398118 | G | A | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1043+5645G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398118 | |||||||
chr9:68398131 | A | C | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1043+5658A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398131 | |||||||
chr9:68398301 | T | A | 184 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(181): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1043+5828T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398301 | |||||||
chr9:68398333 | C | T | 173 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0101 others(170): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.1043+5860C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398333 | |||||||
chr9:68398340 | A | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1043+5867A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398340 | |||||||
chr9:68398350 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+5877A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398350 | |||||||
chr9:68398476 | C | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+6003C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398476 | |||||||
chr9:68398493 | G | T | 58 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(55): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1043+6020G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398493 | |||||||
chr9:68398532 | G | C | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+6059G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398532 | |||||||
chr9:68398661 | C | T | 1 | a0001c0005t0009g0209 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1043+6188C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398661 | |||||||
chr9:68398698 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+6225G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398698 | |||||||
chr9:68398780 | C | A | 1 | a0001c0002t0002g0037 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1043+6307C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398780 | |||||||
chr9:68398785 | T | G | 2 | a0001c0001t0004g0085 a0001c0001t0028g0040 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1043+6312T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398785 | |||||||
chr9:68398808 | C | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+6335C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398808 | |||||||
chr9:68398856 | T | C | 5 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 others(2): Show |
5 | HG02109.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+6383T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398856 | |||||||
chr9:68398884 | T | C | 2 | a0001c0001t0004g0085 a0001c0001t0028g0040 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1043+6411T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398884 | |||||||
chr9:68398895 | T | C | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1043+6422T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68398895 | |||||||
chr9:68399022 | T | G | 4 | a0001c0001t0007g0188 a0001c0007t0004g0091 a0001c0007t0004g0098 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+6549T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399022 | |||||||
chr9:68399145 | G | A | 3 | a0001c0001t0007g0232 a0001c0001t0007g0233 a0001c0001t0012g0231 |
3 | HG02055.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1043+6672G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399145 | |||||||
chr9:68399225 | G | A | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1043+6752G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399225 | |||||||
chr9:68399315 | G | A | 74 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1043+6842G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399315 | |||||||
chr9:68399356 | G | C | 1 | a0001c0002t0002g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1043+6883G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399356 | |||||||
chr9:68399526 | A | G | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043+7053A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399526 | |||||||
chr9:68399547 | C | T | 2 | a0001c0001t0002g0005 a0001c0001t0006g0008 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1043+7074C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399547 | |||||||
chr9:68399636 | AT | A | 12 | a0001c0001t0001g0144 a0001c0001t0003g0202 a0001c0001t0007g0232 others(9): Show |
12 | HG01169.hp1 HG01255.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1043+7174delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68399636 | ||||||
chr9:68399656 | G | A | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1043+7183G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399656 | |||||||
chr9:68399684 | C | T | 58 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(55): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1043+7211C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399684 | |||||||
chr9:68399685 | G | A | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1043+7212G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399685 | |||||||
chr9:68399796 | G | A | 64 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1043+7323G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68399796 | |||||||
chr9:68400106 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+7633T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400106 | |||||||
chr9:68400266 | C | G | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1043+7793C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400266 | |||||||
chr9:68400280 | C | T | 92 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1043+7807C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400280 | |||||||
chr9:68400291 | C | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+7818C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400291 | |||||||
chr9:68400426 | C | G | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+7953C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400426 | |||||||
chr9:68400456 | T | C | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1043+7983T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400456 | |||||||
chr9:68400466 | T | C | 1 | a0001c0002t0008g0029 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1043+7993T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400466 | |||||||
chr9:68400499 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1043+8026A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400499 | |||||||
chr9:68400637 | A | C | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1043+8164A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400637 | |||||||
chr9:68400668 | A | G | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1043+8195A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400668 | |||||||
chr9:68400689 | G | A | 5 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 others(2): Show |
5 | HG02109.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+8216G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400689 | |||||||
chr9:68400723 | G | A | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+8250G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400723 | |||||||
chr9:68400817 | T | C | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043+8344T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400817 | |||||||
chr9:68400885 | C | T | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1043+8412C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400885 | |||||||
chr9:68400956 | C | T | 1 | a0001c0004t0024g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1043+8483C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68400956 | |||||||
chr9:68401063 | G | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+8590G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401063 | |||||||
chr9:68401077 | G | T | 2 | a0001c0001t0004g0085 a0001c0001t0028g0040 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1043+8604G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401077 | |||||||
chr9:68401107 | TA | T | 242 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1043+8637delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401107 | ||||||
chr9:68401340 | G | A | 1 | a0001c0005t0014g0087 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1043+8867G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401340 | |||||||
chr9:68401477 | C | T | 99 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1043+9004C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401477 | |||||||
chr9:68401559 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1043+9086C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401559 | |||||||
chr9:68401598 | G | T | 1 | a0001c0002t0013g0046 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1043+9125G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401598 | |||||||
chr9:68401629 | A | C | 16 | a0001c0001t0001g0176 a0001c0001t0003g0170 a0001c0001t0003g0190 others(13): Show |
16 | HG00099.hp1 HG00642.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.1043+9156A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401629 | |||||||
chr9:68401642 | T | G | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043+9169T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401642 | |||||||
chr9:68401645 | C | T | 10 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1043+9172C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401645 | |||||||
chr9:68401672 | T | G | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043+9199T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401672 | |||||||
chr9:68401725 | T | A | 64 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1043+9252T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401725 | |||||||
chr9:68401877 | CTATA | C | 11 | a0001c0001t0001g0147 a0001c0001t0001g0164 a0001c0001t0001g0199 others(8): Show |
11 | HG00323.hp2 HG00673.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1043+9414_1043+941 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401877 | ||||||
chr9:68401883 | ATATATAT others(7): Show |
A | 1 | a0001c0006t0001g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1043+9412_1043+942 others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401883 | ||||||
chr9:68401885 | ATATATG | A | 57 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(54): Show |
57 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1043+9414_1043+941 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401885 | ||||||
chr9:68401885 | ATATATGT others(1): Show |
A | 19 | a0001c0001t0003g0204 a0001c0001t0003g0205 a0001c0001t0003g0206 others(16): Show |
19 | HG00099.hp1 HG00642.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1043+9414_1043+942 others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401885 | ||||||
chr9:68401885 | ATATATGT others(3): Show |
A | 78 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(75): Show |
78 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1043+9414_1043+942 others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401885 | ||||||
chr9:68401885 | ATATATGT others(5): Show |
A | 6 | a0001c0001t0003g0166 a0001c0001t0015g0097 a0001c0002t0002g0056 others(3): Show |
6 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043+9414_1043+942 others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401885 | ||||||
chr9:68401885 | ATATATGT others(7): Show |
A | 51 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1043+9414_1043+942 others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401885 | ||||||
chr9:68401885 | ATATATGT others(9): Show |
A | 1 | a0001c0001t0001g0150 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1043+9414_1043+942 others(20): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401885 | ||||||
chr9:68401885 | ATATATGT others(11): Show |
A | 6 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
6 | HG01496.hp1 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1043+9414_1043+943 others(22): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401885 | ||||||
chr9:68401889 | A | G | 3 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0001t0028g0040 |
3 | HG01891.hp1 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+9416A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401889 | |||||||
chr9:68401921 | GTGTGTGT others(3): Show |
G | 1 | a0001c0005t0009g0209 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1043+9450_1043+945 others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401921 | ||||||
chr9:68401923 | GTGTGTGT others(3): Show |
G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+9452_1043+946 others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401923 | ||||||
chr9:68401927 | G | A | 1 | a0001c0002t0023g0061 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1043+9454G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401927 | |||||||
chr9:68401929 | G | A | 4 | a0001c0001t0003g0205 a0001c0001t0019g0001 a0001c0001t0019g0002 others(1): Show |
4 | HG00099.hp1 HG00280.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+9456G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401929 | |||||||
chr9:68401929 | GTATA | G | 26 | a0001c0001t0001g0128 a0001c0001t0001g0164 a0001c0001t0001g0199 others(23): Show |
26 | HG00408.hp1 HG00673.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.1043+9460_1043+946 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68401929 | ||||||
chr9:68401931 | A | G | 117 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.1043+9458A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401931 | |||||||
chr9:68401933 | A | G | 29 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(26): Show |
29 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1043+9460A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401933 | |||||||
chr9:68401988 | C | T | 1 | a0001c0006t0004g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1043+9515C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68401988 | |||||||
chr9:68402083 | C | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+9610C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402083 | |||||||
chr9:68402148 | C | G | 1 | a0004c0018t0006g0237 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1043+9675C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402148 | |||||||
chr9:68402155 | T | C | 1 | a0001c0002t0002g0058 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1043+9682T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402155 | |||||||
chr9:68402179 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1043+9706G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402179 | |||||||
chr9:68402264 | A | AAAAAAAT others(6058): Show |
1 | a0001c0002t0023g0061 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1043+9806_1043+980 others(6069): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68402264 | ||||||
chr9:68402343 | T | G | 174 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1043+9870T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402343 | |||||||
chr9:68402344 | A | T | 174 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1043+9871A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402344 | |||||||
chr9:68402543 | C | A | 1 | a0004c0013t0001g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1043+10070C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402543 | |||||||
chr9:68402616 | A | G | 10 | a0001c0001t0001g0110 a0001c0001t0001g0142 a0001c0001t0001g0162 others(7): Show |
10 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1043+10143A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402616 | |||||||
chr9:68402637 | T | C | 174 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1043+10164T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402637 | |||||||
chr9:68402651 | G | T | 1 | a0004c0013t0001g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1043+10178G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402651 | |||||||
chr9:68402734 | G | A | 91 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1043+10261G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402734 | |||||||
chr9:68402735 | T | C | 5 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 others(2): Show |
5 | HG02109.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+10262T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68402735 | |||||||
chr9:68403143 | C | T | 74 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1043+10670C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403143 | |||||||
chr9:68403161 | G | A | 91 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1043+10688G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403161 | |||||||
chr9:68403207 | C | T | 2 | a0001c0001t0004g0085 a0001c0001t0028g0040 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1043+10734C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403207 | |||||||
chr9:68403238 | C | T | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+10765C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403238 | |||||||
chr9:68403287 | T | A | 1 | a0002c0010t0016g0245 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1043+10814T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403287 | |||||||
chr9:68403288 | G | A | 13 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0082 others(10): Show |
13 | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.1043+10815G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403288 | |||||||
chr9:68403369 | T | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+10896T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403369 | |||||||
chr9:68403448 | C | T | 91 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1043+10975C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403448 | |||||||
chr9:68403452 | C | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+10979C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403452 | |||||||
chr9:68403640 | A | C | 56 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(53): Show |
56 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1043+11167A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403640 | |||||||
chr9:68403659 | A | G | 56 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(53): Show |
56 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1043+11186A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403659 | |||||||
chr9:68403703 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1043+11230C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403703 | |||||||
chr9:68403714 | T | G | 1 | a0001c0002t0002g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1043+11241T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403714 | |||||||
chr9:68403866 | C | T | 2 | a0001c0001t0004g0085 a0001c0001t0028g0040 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1043+11393C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403866 | |||||||
chr9:68403867 | A | G | 62 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(59): Show |
62 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1043+11394A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403867 | |||||||
chr9:68403882 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+11409G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403882 | |||||||
chr9:68403963 | G | A | 58 | a0001c0001t0001g0095 a0001c0001t0002g0071 a0001c0001t0002g0072 others(55): Show |
58 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1043+11490G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68403963 | |||||||
chr9:68404058 | C | T | 1 | a0001c0001t0004g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1043+11585C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404058 | |||||||
chr9:68404059 | G | A | 1 | a0001c0001t0004g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1043+11586G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404059 | |||||||
chr9:68404099 | G | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+11626G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404099 | |||||||
chr9:68404199 | T | C | 64 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1043+11726T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404199 | |||||||
chr9:68404285 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+11812C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404285 | |||||||
chr9:68404326 | G | T | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043+11853G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404326 | |||||||
chr9:68404384 | T | C | 62 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(59): Show |
62 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.1043+11911T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404384 | |||||||
chr9:68404494 | A | G | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043+12021A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404494 | |||||||
chr9:68404542 | C | T | 1 | a0001c0001t0029g0111 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1043+12069C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404542 | |||||||
chr9:68404657 | C | T | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043+12184C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404657 | |||||||
chr9:68404662 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+12189C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404662 | |||||||
chr9:68404665 | T | C | 2 | a0001c0001t0004g0085 a0001c0001t0028g0040 |
2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1043+12192T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404665 | |||||||
chr9:68404756 | T | C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+12283T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404756 | |||||||
chr9:68404877 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+12404A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404877 | |||||||
chr9:68404927 | C | G | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+12454C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68404927 | |||||||
chr9:68405087 | G | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+12614G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405087 | |||||||
chr9:68405178 | A | T | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+12705A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405178 | |||||||
chr9:68405289 | A | G | 56 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(53): Show |
56 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1043+12816A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405289 | |||||||
chr9:68405352 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1043+12879G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405352 | |||||||
chr9:68405372 | C | G | 180 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(177): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1043+12899C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405372 | |||||||
chr9:68405410 | T | C | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+12937T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405410 | |||||||
chr9:68405475 | G | C | 178 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1043+13002G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405475 | |||||||
chr9:68405544 | A | G | 1 | a0001c0002t0002g0024 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1043+13071A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405544 | |||||||
chr9:68405558 | C | T | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+13085C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405558 | |||||||
chr9:68405593 | T | C | 56 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(53): Show |
56 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1043+13120T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405593 | |||||||
chr9:68405620 | C | G | 4 | a0001c0001t0012g0118 a0001c0001t0012g0153 a0001c0001t0017g0221 others(1): Show |
4 | HG02698.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+13147C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405620 | |||||||
chr9:68405651 | G | GCTTCTCC others(4): Show |
178 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1043+13186_1043+13 others(17): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68405651 | ||||||
chr9:68405680 | C | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+13207C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405680 | |||||||
chr9:68405681 | C | A | 1 | a0001c0002t0002g0032 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1043+13208C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405681 | |||||||
chr9:68405731 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1043+13258A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405731 | |||||||
chr9:68405753 | T | C | 56 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(53): Show |
56 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.1043+13280T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405753 | |||||||
chr9:68405787 | G | A | 9 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(6): Show |
9 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1043+13314G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405787 | |||||||
chr9:68405832 | CT | C | 178 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1043+13363delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68405832 | ||||||
chr9:68405853 | C | G | 178 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1043+13380C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405853 | |||||||
chr9:68405872 | A | G | 91 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1043+13399A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405872 | |||||||
chr9:68405910 | G | A | 5 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 others(2): Show |
5 | HG02109.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+13437G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405910 | |||||||
chr9:68405913 | C | T | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043+13440C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405913 | |||||||
chr9:68405914 | G | A | 176 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1043+13441G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405914 | |||||||
chr9:68405924 | C | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+13451C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405924 | |||||||
chr9:68405933 | C | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+13460C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68405933 | |||||||
chr9:68406081 | A | T | 57 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(54): Show |
57 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1043+13608A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406081 | |||||||
chr9:68406194 | C | G | 6 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043+13721C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406194 | |||||||
chr9:68406359 | A | G | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+13886A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406359 | |||||||
chr9:68406363 | T | G | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+13890T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406363 | |||||||
chr9:68406365 | G | A | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+13892G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406365 | |||||||
chr9:68406391 | C | T | 55 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(52): Show |
55 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1043+13918C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406391 | |||||||
chr9:68406432 | C | T | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043+13959C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406432 | |||||||
chr9:68406474 | C | G | 1 | a0001c0001t0010g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1043+14001C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406474 | |||||||
chr9:68406659 | GGTATATA others(11): Show |
G | 4 | a0001c0001t0007g0167 a0001c0002t0002g0021 a0001c0004t0024g0240 others(1): Show |
4 | HG00099.hp2 HG00597.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(24): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406659 | ||||||
chr9:68406660 | GTATATAT others(13): Show |
G | 5 | a0001c0001t0003g0192 a0001c0003t0001g0006 a0001c0003t0001g0011 others(2): Show |
5 | HG01891.hp2 HG03041.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(26): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(15): Show |
G | 2 | a0001c0001t0001g0140 a0001c0004t0006g0241 |
2 | NA18980.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(28): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(17): Show |
G | 1 | a0001c0001t0001g0131 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1043+14205_1043+14 others(30): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(19): Show |
G | 7 | a0001c0001t0001g0096 a0001c0001t0001g0129 a0001c0001t0001g0163 others(4): Show |
7 | HG00423.hp2 HG00639.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(32): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(21): Show |
G | 14 | a0001c0001t0001g0099 a0001c0001t0001g0112 a0001c0001t0001g0123 others(11): Show |
14 | HG00639.hp2 HG00642.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(34): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(23): Show |
G | 28 | a0001c0001t0001g0093 a0001c0001t0001g0121 a0001c0001t0001g0127 others(25): Show |
28 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(36): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(25): Show |
G | 10 | a0001c0001t0010g0214 a0001c0001t0010g0223 a0001c0001t0010g0228 others(7): Show |
10 | HG00323.hp2 HG00408.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(38): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(27): Show |
G | 11 | a0001c0001t0001g0175 a0001c0001t0003g0166 a0001c0001t0004g0085 others(8): Show |
11 | HG02027.hp1 HG02155.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(40): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(29): Show |
G | 4 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0005t0014g0087 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(42): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(31): Show |
G | 3 | a0001c0001t0001g0142 a0001c0001t0004g0178 a0001c0002t0002g0062 |
3 | HG00738.hp2 HG00741.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(44): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(35): Show |
G | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1043+14205_1043+14 others(48): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406660 | GTATATAT others(39): Show |
G | 3 | a0001c0005t0009g0208 a0001c0005t0009g0209 a0001c0005t0009g0210 |
3 | HG01255.hp2 HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(52): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406660 | ||||||
chr9:68406662 | A | G | 5 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+14189A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406662 | |||||||
chr9:68406662 | ATATATAT others(9): Show |
A | 7 | a0001c0001t0001g0182 a0001c0001t0006g0075 a0001c0001t0006g0076 others(4): Show |
7 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(22): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406662 | ||||||
chr9:68406664 | ATATATAT others(7): Show |
A | 17 | a0001c0001t0001g0100 a0001c0001t0001g0173 a0001c0001t0001g0176 others(14): Show |
17 | HG00735.hp2 HG01243.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(20): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406664 | ||||||
chr9:68406666 | ATATATAT others(5): Show |
A | 16 | a0001c0001t0001g0086 a0001c0001t0001g0110 a0001c0001t0001g0114 others(13): Show |
16 | HG00280.hp2 HG00741.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406666 | ||||||
chr9:68406668 | ATATATAT others(3): Show |
A | 24 | a0001c0001t0001g0108 a0001c0001t0001g0160 a0001c0001t0001g0186 others(21): Show |
24 | HG01109.hp2 HG01175.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406668 | ||||||
chr9:68406670 | ATATATAT others(1): Show |
A | 18 | a0001c0001t0001g0101 a0001c0001t0001g0180 a0001c0001t0001g0183 others(15): Show |
18 | HG00140.hp2 HG01106.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406670 | ||||||
chr9:68406672 | ATATATG | A | 21 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0115 others(18): Show |
21 | HG01109.hp1 HG01261.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406672 | ||||||
chr9:68406674 | ATATG | A | 12 | a0001c0001t0001g0124 a0001c0001t0001g0181 a0001c0001t0005g0141 others(9): Show |
12 | HG00408.hp2 HG00438.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406674 | ||||||
chr9:68406676 | A | ATATATAT others(23): Show |
1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1043+14204_1043+14 others(36): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406676 | ||||||
chr9:68406676 | ATG | A | 11 | a0001c0001t0001g0185 a0001c0001t0002g0071 a0001c0001t0003g0195 others(8): Show |
11 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(8): Show |
intron_variant | MODIFIER | c.1043+14205_1043+14 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406676 | ||||||
chr9:68406678 | G | A | 23 | a0001c0001t0002g0082 a0001c0001t0003g0120 a0001c0001t0003g0170 others(20): Show |
23 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1043+14205G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406678 | |||||||
chr9:68406692 | A | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+14219A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406692 | |||||||
chr9:68406694 | A | G | 1 | a0001c0002t0013g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1043+14221A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406694 | |||||||
chr9:68406718 | A | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+14245A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406718 | |||||||
chr9:68406720 | A | ATATATAT others(5): Show |
1 | a0001c0002t0002g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1043+14252_1043+14 others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406720 | ||||||
chr9:68406720 | A | ATATG | 5 | a0001c0001t0002g0082 a0001c0002t0002g0015 a0001c0002t0002g0037 others(2): Show |
5 | HG01081.hp2 HG02056.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+14250_1043+14 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406720 | ||||||
chr9:68406720 | A | ATG | 5 | a0001c0001t0003g0170 a0001c0002t0002g0038 a0001c0002t0002g0059 others(2): Show |
5 | HG00735.hp1 HG01071.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+14248_1043+14 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68406720 | ||||||
chr9:68406720 | A | G | 79 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1043+14247A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406720 | |||||||
chr9:68406722 | A | G | 67 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(64): Show |
67 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1043+14249A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406722 | |||||||
chr9:68406740 | C | G | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1043+14267C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406740 | |||||||
chr9:68406757 | A | G | 34 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(31): Show |
34 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.1043+14284A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406757 | |||||||
chr9:68406758 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+14285G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406758 | |||||||
chr9:68406871 | G | A | 58 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(55): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1043+14398G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406871 | |||||||
chr9:68406949 | G | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+14476G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406949 | |||||||
chr9:68406977 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+14504T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406977 | |||||||
chr9:68406978 | C | T | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1043+14505C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68406978 | |||||||
chr9:68407081 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+14608A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407081 | |||||||
chr9:68407086 | T | G | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1043+14613T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407086 | |||||||
chr9:68407133 | G | C | 242 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1043+14660G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407133 | |||||||
chr9:68407136 | C | T | 1 | a0001c0001t0004g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1043+14663C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407136 | |||||||
chr9:68407137 | G | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+14664G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407137 | |||||||
chr9:68407334 | C | T | 1 | a0001c0002t0002g0035 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1043+14861C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407334 | |||||||
chr9:68407570 | TG | T | 9 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(6): Show |
9 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.1043+15100delG | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68407570 | ||||||
chr9:68407640 | A | G | 1 | a0001c0001t0029g0111 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1043+15167A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407640 | |||||||
chr9:68407723 | A | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+15250A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407723 | |||||||
chr9:68407739 | G | T | 32 | a0001c0001t0001g0176 a0001c0001t0003g0120 a0001c0001t0003g0166 others(29): Show |
32 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1043+15266G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407739 | |||||||
chr9:68407821 | C | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+15348C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407821 | |||||||
chr9:68407935 | A | G | 3 | a0001c0001t0010g0216 a0001c0001t0010g0217 a0001c0001t0011g0212 |
3 | HG02027.hp1 NA18980.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1043+15462A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68407935 | |||||||
chr9:68408047 | T | C | 1 | a0001c0002t0002g0021 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1043+15574T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408047 | |||||||
chr9:68408050 | T | C | 32 | a0001c0001t0001g0176 a0001c0001t0003g0120 a0001c0001t0003g0166 others(29): Show |
32 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1043+15577T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408050 | |||||||
chr9:68408208 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1043+15735G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408208 | |||||||
chr9:68408418 | G | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+15945G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408418 | |||||||
chr9:68408576 | G | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+16103G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408576 | |||||||
chr9:68408612 | C | T | 2 | a0001c0002t0002g0041 a0001c0002t0002g0042 |
2 | HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1043+16139C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408612 | |||||||
chr9:68408711 | G | A | 4 | a0001c0001t0007g0188 a0001c0007t0004g0091 a0001c0007t0004g0098 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+16238G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408711 | |||||||
chr9:68408733 | T | C | 1 | a0001c0001t0006g0008 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1043+16260T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408733 | |||||||
chr9:68408756 | G | A | 3 | a0001c0001t0028g0040 a0001c0002t0002g0003 a0001c0002t0002g0004 |
3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+16283G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408756 | |||||||
chr9:68408873 | A | C | 2 | a0001c0001t0015g0097 a0001c0001t0015g0116 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1043+16400A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408873 | |||||||
chr9:68408894 | G | A | 4 | a0001c0001t0007g0188 a0001c0007t0004g0091 a0001c0007t0004g0098 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+16421G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68408894 | |||||||
chr9:68409131 | T | C | 55 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(52): Show |
55 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1043+16658T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409131 | |||||||
chr9:68409176 | T | C | 6 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043+16703T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409176 | |||||||
chr9:68409278 | G | T | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+16805G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409278 | |||||||
chr9:68409317 | C | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+16844C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409317 | |||||||
chr9:68409425 | C | T | 32 | a0001c0001t0001g0176 a0001c0001t0003g0120 a0001c0001t0003g0166 others(29): Show |
32 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1043+16952C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409425 | |||||||
chr9:68409443 | T | C | 7 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
7 | HG02572.hp2 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1043+16970T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409443 | |||||||
chr9:68409452 | A | G | 1 | a0001c0002t0008g0034 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1043+16979A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409452 | |||||||
chr9:68409481 | T | C | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+17008T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409481 | |||||||
chr9:68409496 | C | G | 1 | a0001c0001t0003g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1043+17023C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409496 | |||||||
chr9:68409498 | G | A | 3 | a0001c0001t0028g0040 a0001c0002t0002g0003 a0001c0002t0002g0004 |
3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+17025G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409498 | |||||||
chr9:68409626 | CA | C | 174 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1043+17159delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68409626 | ||||||
chr9:68409632 | A | G | 174 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1043+17159A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409632 | |||||||
chr9:68409671 | A | G | 174 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1043+17198A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409671 | |||||||
chr9:68409684 | A | G | 4 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(1): Show |
4 | NA18963.hp2 NA18992.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+17211A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409684 | |||||||
chr9:68409731 | G | C | 1 | a0001c0005t0009g0210 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1043+17258G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409731 | |||||||
chr9:68409737 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1043+17264A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409737 | |||||||
chr9:68409782 | G | A | 2 | a0001c0001t0004g0085 a0004c0013t0001g0146 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1043+17309G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409782 | |||||||
chr9:68409799 | C | G | 177 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(174): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1043+17326C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409799 | |||||||
chr9:68409823 | T | C | 1 | a0001c0002t0008g0025 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1043+17350T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409823 | |||||||
chr9:68409850 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1043+17377A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409850 | |||||||
chr9:68409872 | T | TA | 13 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0002t0002g0003 others(10): Show |
13 | HG01255.hp2 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1043+17415dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68409872 | ||||||
chr9:68409872 | TA | T | 156 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0096 others(153): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1043+17415delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68409872 | ||||||
chr9:68409919 | T | C | 5 | a0001c0001t0001g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 others(2): Show |
5 | HG02257.hp2 HG03195.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1043+17446T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409919 | |||||||
chr9:68409938 | T | A | 10 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1043+17465T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409938 | |||||||
chr9:68409939 | C | T | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043+17466C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68409939 | |||||||
chr9:68410037 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1043+17564G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410037 | |||||||
chr9:68410191 | T | A | 99 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1043+17718T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410191 | |||||||
chr9:68410244 | A | G | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+17771A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410244 | |||||||
chr9:68410268 | AG | A | 52 | a0001c0001t0001g0095 a0001c0001t0002g0071 a0001c0001t0002g0072 others(49): Show |
52 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1043+17798delG | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68410268 | ||||||
chr9:68410309 | G | A | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1043+17836G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410309 | |||||||
chr9:68410440 | A | G | 237 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1043+17967A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410440 | |||||||
chr9:68410484 | TTAGAC | T | 6 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043+18014_1043+18 others(11): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68410484 | ||||||
chr9:68410520 | C | G | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+18047C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410520 | |||||||
chr9:68410558 | TGAG | T | 3 | a0001c0001t0028g0040 a0001c0002t0002g0003 a0001c0002t0002g0004 |
3 | HG02559.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+18107_1043+18 others(9): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68410558 | ||||||
chr9:68410558 | TGAGGAGG others(5): Show |
T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+18098_1043+18 others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68410558 | ||||||
chr9:68410559 | G | C | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1043+18086G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410559 | |||||||
chr9:68410561 | G | T | 76 | a0001c0001t0001g0086 a0001c0001t0001g0100 a0001c0001t0001g0101 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1043+18088G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410561 | |||||||
chr9:68410564 | G | T | 6 | a0001c0001t0028g0040 a0001c0002t0002g0003 a0001c0002t0002g0004 others(3): Show |
6 | HG02559.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1043+18091G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410564 | |||||||
chr9:68410616 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1043+18143G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410616 | |||||||
chr9:68410926 | G | C | 10 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1043+18453G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68410926 | |||||||
chr9:68411375 | G | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0173 |
3 | HG02129.hp1 NA18612.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1043+18902G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68411375 | |||||||
chr9:68411381 | A | AT | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+18909dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411381 | ||||||
chr9:68411396 | C | T | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1043+18923C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68411396 | |||||||
chr9:68411398 | CACACATA others(29): Show |
C | 54 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(51): Show |
54 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043+18936_1043+18 others(42): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411398 | ||||||
chr9:68411400 | CACATATA others(27): Show |
C | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1043+18931_1043+18 others(40): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411400 | ||||||
chr9:68411465 | A | C | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1043+18992A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68411465 | |||||||
chr9:68411468 | ATG | A | 59 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(56): Show |
59 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.1043+19015_1043+19 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411468 | ||||||
chr9:68411484 | G | GTATATAT others(1): Show |
8 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(5): Show |
8 | HG00642.hp1 HG01081.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+19012_1043+19 others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411484 | ||||||
chr9:68411484 | G | GTATATAT others(5): Show |
1 | a0001c0003t0005g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1043+19012_1043+19 others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411484 | ||||||
chr9:68411486 | G | A | 78 | a0001c0001t0001g0086 a0001c0001t0001g0100 a0001c0001t0001g0101 others(75): Show |
78 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1043+19013G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68411486 | |||||||
chr9:68411486 | G | GTA | 10 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0004t0002g0238 others(7): Show |
10 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1043+19014_1043+19 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411486 | ||||||
chr9:68411486 | G | GTATATAT others(1): Show |
50 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(47): Show |
50 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.1043+19014_1043+19 others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411486 | ||||||
chr9:68411486 | G | GTATATAT others(3): Show |
31 | a0001c0001t0003g0120 a0001c0001t0003g0170 a0001c0001t0003g0172 others(28): Show |
31 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.1043+19014_1043+19 others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411486 | ||||||
chr9:68411486 | G | GTATATAT others(5): Show |
4 | a0001c0001t0003g0190 a0001c0001t0007g0232 a0001c0001t0014g0094 others(1): Show |
4 | HG01346.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+19014_1043+19 others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411486 | ||||||
chr9:68411486 | G | GTATATAT others(7): Show |
1 | a0001c0002t0008g0029 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1043+19014_1043+19 others(20): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411486 | ||||||
chr9:68411488 | G | A | 239 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(236): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1043+19015G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68411488 | |||||||
chr9:68411488 | G | GTATATAT others(3): Show |
1 | a0001c0002t0002g0057 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1043+19021_1043+19 others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68411488 | ||||||
chr9:68411641 | T | C | 2 | a0001c0001t0001g0108 a0001c0002t0008g0044 |
2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1043+19168T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68411641 | |||||||
chr9:68411642 | C | G | 2 | a0001c0001t0001g0108 a0001c0002t0008g0044 |
2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1043+19169C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68411642 | |||||||
chr9:68411691 | A | G | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+19218A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68411691 | |||||||
chr9:68411975 | A | G | 1 | a0001c0001t0021g0207 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1043+19502A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68411975 | |||||||
chr9:68412048 | C | G | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1043+19575C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68412048 | |||||||
chr9:68412110 | C | T | 52 | a0001c0001t0001g0095 a0001c0001t0002g0071 a0001c0001t0002g0072 others(49): Show |
52 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1043+19637C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68412110 | |||||||
chr9:68412243 | A | G | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+19770A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68412243 | |||||||
chr9:68412372 | A | G | 1 | a0001c0001t0018g0227 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1043+19899A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68412372 | |||||||
chr9:68412389 | T | C | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+19916T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68412389 | |||||||
chr9:68412649 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+20176G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68412649 | |||||||
chr9:68412683 | C | T | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043+20210C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68412683 | |||||||
chr9:68412715 | T | C | 39 | a0001c0001t0001g0176 a0001c0001t0003g0120 a0001c0001t0003g0166 others(36): Show |
39 | HG00099.hp1 HG00597.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1043+20242T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68412715 | |||||||
chr9:68412813 | C | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+20340C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68412813 | |||||||
chr9:68412826 | T | C | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1043+20353T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68412826 | |||||||
chr9:68413028 | G | A | 67 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(64): Show |
67 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.1043+20555G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413028 | |||||||
chr9:68413140 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1043+20667A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413140 | |||||||
chr9:68413211 | A | G | 91 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1043+20738A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413211 | |||||||
chr9:68413222 | T | G | 7 | a0001c0001t0001g0121 a0001c0001t0029g0111 a0001c0002t0002g0003 others(4): Show |
7 | HG01255.hp2 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1043+20749T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413222 | |||||||
chr9:68413283 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+20810T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413283 | |||||||
chr9:68413342 | T | C | 118 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1043+20869T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413342 | |||||||
chr9:68413343 | G | A | 7 | a0001c0001t0007g0232 a0001c0001t0007g0233 a0001c0001t0009g0211 others(4): Show |
7 | HG02055.hp2 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1043+20870G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413343 | |||||||
chr9:68413359 | A | G | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+20886A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413359 | |||||||
chr9:68413360 | A | G | 3 | a0001c0001t0007g0232 a0001c0001t0007g0233 a0001c0001t0012g0231 |
3 | HG02055.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1043+20887A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413360 | |||||||
chr9:68413427 | A | T | 5 | a0001c0001t0001g0102 a0001c0001t0004g0103 a0001c0001t0004g0104 others(2): Show |
5 | HG02257.hp2 HG03195.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1043+20954A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413427 | |||||||
chr9:68413502 | A | G | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+21029A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413502 | |||||||
chr9:68413566 | G | A | 1 | a0001c0001t0004g0085 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1043+21093G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413566 | |||||||
chr9:68413638 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+21165A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413638 | |||||||
chr9:68413790 | A | T | 1 | a0001c0019t0006g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1043+21317A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413790 | |||||||
chr9:68413911 | C | T | 91 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0002g0071 others(88): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1043+21438C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413911 | |||||||
chr9:68413952 | G | A | 55 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(52): Show |
55 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1043+21479G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68413952 | |||||||
chr9:68414018 | G | C | 1 | a0001c0003t0005g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1043+21545G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414018 | |||||||
chr9:68414270 | G | C | 1 | a0001c0002t0008g0025 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1043+21797G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414270 | |||||||
chr9:68414335 | G | T | 3 | a0001c0001t0010g0216 a0001c0001t0010g0217 a0001c0001t0011g0212 |
3 | HG02027.hp1 NA18980.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1043+21862G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414335 | |||||||
chr9:68414420 | A | G | 3 | a0001c0004t0002g0242 a0001c0004t0006g0241 a0001c0004t0006g0244 |
3 | HG01891.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1043+21947A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414420 | |||||||
chr9:68414614 | C | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0006g0008 others(1): Show |
4 | HG02258.hp2 HG02572.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+22141C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414614 | |||||||
chr9:68414684 | C | G | 238 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.1043+22211C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414684 | |||||||
chr9:68414711 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1043+22238C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414711 | |||||||
chr9:68414800 | A | G | 235 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(232): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1043+22327A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414800 | |||||||
chr9:68414883 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0005g0130 a0001c0012t0001g0109 |
3 | HG02056.hp1 NA18955.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1043+22410C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414883 | |||||||
chr9:68414952 | T | C | 71 | a0001c0001t0001g0086 a0001c0001t0001g0100 a0001c0001t0001g0101 others(68): Show |
71 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1043+22479T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414952 | |||||||
chr9:68414954 | T | C | 1 | a0001c0001t0003g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1043+22481T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414954 | |||||||
chr9:68414977 | T | A | 41 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(38): Show |
41 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1043+22504T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414977 | |||||||
chr9:68414985 | A | G | 41 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(38): Show |
41 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1043+22512A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414985 | |||||||
chr9:68414996 | C | T | 1 | a0001c0002t0002g0049 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1043+22523C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414996 | |||||||
chr9:68414999 | A | G | 41 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(38): Show |
41 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1043+22526A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68414999 | |||||||
chr9:68415035 | G | A | 7 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0133 others(4): Show |
7 | HG00609.hp1 HG01175.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1043+22562G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415035 | |||||||
chr9:68415082 | T | G | 1 | a0001c0003t0005g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1043+22609T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415082 | |||||||
chr9:68415177 | A | G | 72 | a0001c0001t0001g0086 a0001c0001t0001g0100 a0001c0001t0001g0101 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1043+22704A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415177 | |||||||
chr9:68415206 | T | C | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+22733T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415206 | |||||||
chr9:68415216 | A | G | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+22743A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415216 | |||||||
chr9:68415220 | A | G | 33 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(30): Show |
33 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1043+22747A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415220 | |||||||
chr9:68415349 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1043+22876T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415349 | |||||||
chr9:68415508 | T | C | 9 | a0001c0001t0001g0163 a0001c0004t0002g0238 a0001c0004t0002g0242 others(6): Show |
9 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1043+23035T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415508 | |||||||
chr9:68415549 | T | C | 1 | a0001c0002t0008g0029 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1043+23076T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415549 | |||||||
chr9:68415598 | G | T | 242 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1043+23125G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415598 | |||||||
chr9:68415755 | A | G | 10 | a0001c0003t0001g0006 a0001c0003t0001g0011 a0001c0003t0001g0017 others(7): Show |
10 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.1043+23282A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415755 | |||||||
chr9:68415779 | A | ATATC | 4 | a0001c0001t0005g0130 a0001c0001t0012g0153 a0001c0002t0002g0058 others(1): Show |
4 | HG02647.hp2 HG03654.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+23340_1043+23 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68415779 | ||||||
chr9:68415779 | A | ATATCTAT others(1): Show |
36 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(33): Show |
36 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1043+23336_1043+23 others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68415779 | ||||||
chr9:68415779 | A | ATATCTAT others(5): Show |
57 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0132 others(54): Show |
57 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.1043+23332_1043+23 others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68415779 | ||||||
chr9:68415779 | A | ATATCTAT others(9): Show |
33 | a0001c0001t0001g0121 a0001c0001t0001g0143 a0001c0001t0001g0199 others(30): Show |
33 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1043+23328_1043+23 others(22): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68415779 | ||||||
chr9:68415779 | A | ATATCTAT others(13): Show |
31 | a0001c0001t0002g0071 a0001c0001t0007g0168 a0001c0001t0009g0119 others(28): Show |
31 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.1043+23324_1043+23 others(26): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68415779 | ||||||
chr9:68415779 | A | ATATCTAT others(17): Show |
9 | a0001c0001t0001g0095 a0001c0001t0002g0082 a0001c0001t0007g0169 others(6): Show |
9 | HG00408.hp2 HG01106.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1043+23320_1043+23 others(30): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68415779 | ||||||
chr9:68415779 | A | ATATCTAT others(21): Show |
1 | a0001c0001t0019g0001 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1043+23316_1043+23 others(34): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68415779 | ||||||
chr9:68415779 | ATATCTAT others(5): Show |
A | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+23332_1043+23 others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68415779 | ||||||
chr9:68415793 | A | ATCTATCT others(5): Show |
58 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(55): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1043+23331_1043+23 others(18): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68415793 | ||||||
chr9:68415831 | C | T | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1043+23358C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415831 | |||||||
chr9:68415938 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+23465A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68415938 | |||||||
chr9:68416277 | A | T | 1 | a0001c0001t0007g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1043+23804A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416277 | |||||||
chr9:68416289 | G | A | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1043+23816G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416289 | |||||||
chr9:68416309 | A | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0184 |
2 | HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1043+23836A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416309 | |||||||
chr9:68416317 | G | A | 1 | a0001c0001t0014g0094 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1043+23844G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416317 | |||||||
chr9:68416335 | T | C | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1043+23862T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416335 | |||||||
chr9:68416402 | G | T | 53 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(50): Show |
53 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1043+23929G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416402 | |||||||
chr9:68416612 | T | C | 9 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0080 others(6): Show |
9 | HG00280.hp2 HG00609.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1043+24139T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416612 | |||||||
chr9:68416616 | G | A | 5 | a0001c0005t0004g0089 a0001c0005t0014g0087 a0001c0005t0014g0088 others(2): Show |
5 | HG02109.hp1 HG03041.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+24143G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416616 | |||||||
chr9:68416659 | G | A | 2 | a0001c0001t0003g0195 a0001c0001t0003g0196 |
2 | HG00642.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1043+24186G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416659 | |||||||
chr9:68416684 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1043+24211T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416684 | |||||||
chr9:68416734 | T | C | 92 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0001g0199 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1043+24261T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416734 | |||||||
chr9:68416742 | G | T | 3 | a0001c0001t0004g0085 a0001c0002t0002g0003 a0001c0002t0002g0004 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+24269G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416742 | |||||||
chr9:68416815 | A | T | 242 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1043+24342A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416815 | |||||||
chr9:68416818 | C | T | 1 | a0001c0002t0002g0028 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1043+24345C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416818 | |||||||
chr9:68416929 | A | T | 53 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(50): Show |
53 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1043+24456A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68416929 | |||||||
chr9:68417126 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1043+24653C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68417126 | |||||||
chr9:68417136 | C | T | 1 | a0001c0001t0003g0192 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1043+24663C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68417136 | |||||||
chr9:68417151 | A | C | 1 | a0001c0001t0029g0111 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1043+24678A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68417151 | |||||||
chr9:68417158 | T | A | 1 | a0001c0001t0001g0174 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1043+24685T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68417158 | |||||||
chr9:68417371 | C | G | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1043+24898C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68417371 | |||||||
chr9:68417422 | C | CG | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+24954dupG | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68417422 | ||||||
chr9:68417507 | T | G | 3 | a0001c0001t0004g0085 a0001c0002t0002g0003 a0001c0002t0002g0004 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1043+25034T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68417507 | |||||||
chr9:68417682 | C | A | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1043+25209C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68417682 | |||||||
chr9:68417863 | CT | C | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+25391delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68417863 | |||||||
chr9:68418068 | G | C | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+25595G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68418068 | |||||||
chr9:68418127 | C | T | 8 | a0001c0004t0002g0238 a0001c0004t0002g0242 a0001c0004t0002g0243 others(5): Show |
8 | HG01175.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1043+25654C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68418127 | |||||||
chr9:68418393 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+25920C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68418393 | |||||||
chr9:68418585 | C | T | 123 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(120): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1043+26112C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68418585 | |||||||
chr9:68418622 | T | C | 129 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(126): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1043+26149T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68418622 | |||||||
chr9:68418648 | T | A | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1043+26175T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68418648 | |||||||
chr9:68418648 | T | TTGGC | 5 | a0001c0005t0009g0208 a0001c0005t0009g0209 a0001c0005t0009g0210 others(2): Show |
5 | HG01255.hp2 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+26177_1043+26 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68418648 | ||||||
chr9:68418651 | A | G | 5 | a0001c0005t0009g0208 a0001c0005t0009g0209 a0001c0005t0009g0210 others(2): Show |
5 | HG01255.hp2 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+26178A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68418651 | |||||||
chr9:68418735 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1043+26262C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68418735 | |||||||
chr9:68418920 | A | G | 57 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(54): Show |
57 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1043+26447A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68418920 | |||||||
chr9:68418983 | C | T | 3 | a0001c0004t0024g0240 a0001c0004t0025g0236 a0004c0018t0006g0237 |
3 | HG01175.hp1 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1043+26510C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68418983 | |||||||
chr9:68419063 | T | C | 2 | a0001c0005t0009g0208 a0001c0005t0009g0210 |
2 | HG01255.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1043+26590T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419063 | |||||||
chr9:68419096 | A | G | 7 | a0001c0003t0005g0007 a0001c0003t0005g0012 a0001c0003t0005g0013 others(4): Show |
7 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1043+26623A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419096 | |||||||
chr9:68419287 | C | T | 53 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(50): Show |
53 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.1043+26814C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419287 | |||||||
chr9:68419294 | C | A | 3 | a0001c0004t0024g0240 a0001c0004t0025g0236 a0004c0018t0006g0237 |
3 | HG01175.hp1 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1043+26821C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419294 | |||||||
chr9:68419311 | A | G | 2 | a0001c0005t0014g0087 a0001c0005t0014g0088 |
2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1043+26838A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419311 | |||||||
chr9:68419395 | G | A | 1 | a0001c0002t0023g0061 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1043+26922G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419395 | |||||||
chr9:68419447 | T | C | 116 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0101 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.1043+26974T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419447 | |||||||
chr9:68419561 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1043+27088C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419561 | |||||||
chr9:68419563 | G | A | 1 | a0001c0002t0002g0030 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1043+27090G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419563 | |||||||
chr9:68419816 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1043+27343C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419816 | |||||||
chr9:68419878 | A | G | 6 | a0001c0001t0001g0100 a0001c0001t0001g0139 a0001c0001t0001g0200 others(3): Show |
6 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043+27405A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68419878 | |||||||
chr9:68420158 | C | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+27685C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68420158 | |||||||
chr9:68420220 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1043+27747G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68420220 | |||||||
chr9:68420536 | C | T | 114 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1043+28063C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68420536 | |||||||
chr9:68420585 | A | C | 5 | a0001c0001t0020g0156 a0001c0001t0020g0157 a0001c0003t0005g0007 others(2): Show |
5 | HG00642.hp1 HG01081.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1043+28112A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68420585 | |||||||
chr9:68420656 | T | A | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1043+28183T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68420656 | |||||||
chr9:68420671 | C | G | 1 | a0001c0004t0002g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1043+28198C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68420671 | |||||||
chr9:68420721 | G | A | 1 | a0001c0001t0005g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1043+28248G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68420721 | |||||||
chr9:68420787 | T | C | 101 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(98): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1043+28314T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68420787 | |||||||
chr9:68420831 | T | G | 2 | a0001c0001t0002g0070 a0001c0001t0009g0119 |
2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1043+28358T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68420831 | |||||||
chr9:68421022 | A | G | 106 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(103): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1043+28549A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421022 | |||||||
chr9:68421091 | T | C | 134 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(131): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1043+28618T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421091 | |||||||
chr9:68421138 | C | T | 10 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(7): Show |
10 | HG00323.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1043+28665C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421138 | |||||||
chr9:68421178 | C | G | 1 | a0001c0001t0001g0186 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1043+28705C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421178 | |||||||
chr9:68421179 | G | A | 1 | a0001c0003t0005g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1043+28706G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421179 | |||||||
chr9:68421208 | T | C | 1 | a0001c0002t0002g0064 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1043+28735T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421208 | |||||||
chr9:68421456 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1043+28983G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421456 | |||||||
chr9:68421499 | C | T | 7 | a0001c0001t0004g0151 a0001c0001t0019g0001 a0001c0001t0019g0002 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1043+29026C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421499 | |||||||
chr9:68421588 | G | A | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1043+29115G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421588 | |||||||
chr9:68421760 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1043+29287A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421760 | |||||||
chr9:68421979 | C | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+29506C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68421979 | |||||||
chr9:68422108 | T | A | 1 | a0001c0001t0005g0158 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1043+29635T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422108 | |||||||
chr9:68422151 | C | A | 2 | a0001c0001t0001g0095 a0001c0002t0002g0031 |
2 | HG00438.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1043+29678C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422151 | |||||||
chr9:68422174 | G | A | 3 | a0001c0005t0009g0208 a0001c0005t0009g0210 a0001c0020t0030g0090 |
3 | HG01255.hp2 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1043+29701G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422174 | |||||||
chr9:68422189 | T | C | 20 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(17): Show |
20 | HG00423.hp2 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1043+29716T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422189 | |||||||
chr9:68422190 | C | T | 20 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(17): Show |
20 | HG00423.hp2 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1043+29717C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422190 | |||||||
chr9:68422214 | A | C | 1 | a0001c0001t0001g0160 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1043+29741A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422214 | |||||||
chr9:68422324 | A | G | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1043+29851A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422324 | |||||||
chr9:68422379 | T | TACCTCTT others(7): Show |
5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+29908_1043+29 others(20): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68422379 | ||||||
chr9:68422457 | GTTTTGTT | G | 4 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0004t0002g0238 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+29996_1043+30 others(13): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68422457 | ||||||
chr9:68422461 | TG | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+29989delG | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422461 | |||||||
chr9:68422593 | G | A | 1 | a0001c0002t0002g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1043+30120G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422593 | |||||||
chr9:68422714 | A | G | 239 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(236): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1043+30241A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422714 | |||||||
chr9:68422814 | G | A | 1 | a0001c0002t0008g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1043+30341G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422814 | |||||||
chr9:68422860 | C | T | 99 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1043+30387C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422860 | |||||||
chr9:68422891 | C | T | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1043+30418C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422891 | |||||||
chr9:68422899 | C | T | 7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(4): Show |
7 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1043+30426C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422899 | |||||||
chr9:68422946 | C | A | 1 | a0001c0002t0002g0066 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1043+30473C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68422946 | |||||||
chr9:68423119 | G | A | 4 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0004t0025g0236 others(1): Show |
4 | HG01175.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+30646G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423119 | |||||||
chr9:68423190 | T | TGCAAGTA others(6126): Show |
1 | a0001c0002t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1043+30732_1043+30 others(6139): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68423190 | ||||||
chr9:68423206 | G | A | 102 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(99): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1043+30733G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423206 | |||||||
chr9:68423375 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1043+30902C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423375 | |||||||
chr9:68423543 | G | T | 99 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1043+31070G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423543 | |||||||
chr9:68423546 | T | C | 102 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(99): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1043+31073T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423546 | |||||||
chr9:68423647 | C | G | 3 | a0001c0003t0005g0007 a0001c0003t0005g0012 a0001c0003t0005g0013 |
3 | HG00642.hp1 HG01081.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1043+31174C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423647 | |||||||
chr9:68423649 | C | CTCTCTCT others(9): Show |
4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+31181_1043+31 others(22): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68423649 | ||||||
chr9:68423649 | C | G | 1 | a0001c0006t0004g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1043+31176C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423649 | |||||||
chr9:68423651 | C | CTCTCTCT others(13): Show |
3 | a0001c0001t0004g0154 a0001c0005t0014g0087 a0001c0005t0014g0088 |
3 | HG03225.hp2 HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1043+31181_1043+31 others(26): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68423651 | ||||||
chr9:68423651 | C | CTCTCTCT others(11): Show |
1 | a0001c0004t0024g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1043+31181_1043+31 others(24): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68423651 | ||||||
chr9:68423651 | C | CTCTCTCT others(9): Show |
5 | a0001c0001t0014g0094 a0001c0002t0002g0003 a0001c0002t0002g0004 others(2): Show |
5 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+31181_1043+31 others(22): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68423651 | ||||||
chr9:68423651 | CTCTG | C | 9 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0185 others(6): Show |
9 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.1043+31182_1043+31 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68423651 | ||||||
chr9:68423655 | G | C | 19 | a0001c0001t0001g0160 a0001c0001t0004g0103 a0001c0001t0004g0104 others(16): Show |
19 | HG00323.hp2 HG02109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1043+31182G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423655 | |||||||
chr9:68423655 | GTC | G | 16 | a0001c0001t0002g0073 a0001c0001t0002g0080 a0001c0001t0004g0178 others(13): Show |
16 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1043+31208_1043+31 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68423655 | ||||||
chr9:68423655 | GTCTCTC | G | 93 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(90): Show |
93 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1043+31204_1043+31 others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68423655 | ||||||
chr9:68423657 | C | G | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1043+31184C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423657 | |||||||
chr9:68423661 | C | G | 9 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0173 others(6): Show |
9 | HG00140.hp1 HG00140.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1043+31188C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423661 | |||||||
chr9:68423671 | C | G | 99 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1043+31198C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423671 | |||||||
chr9:68423687 | C | T | 1 | a0001c0001t0015g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1043+31214C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423687 | |||||||
chr9:68423774 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1043+31301C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423774 | |||||||
chr9:68423777 | C | T | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1043+31304C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423777 | |||||||
chr9:68423916 | G | A | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+31443G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68423916 | |||||||
chr9:68424006 | A | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1043+31533A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68424006 | |||||||
chr9:68424027 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1043+31554C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68424027 | |||||||
chr9:68424128 | A | T | 155 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(152): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1043+31655A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68424128 | |||||||
chr9:68424260 | A | G | 5 | a0001c0001t0011g0215 a0001c0002t0002g0036 a0001c0002t0002g0037 others(2): Show |
5 | HG02056.hp2 HG02080.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1043+31787A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68424260 | |||||||
chr9:68424509 | G | T | 1 | a0001c0001t0006g0079 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1043+32036G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68424509 | |||||||
chr9:68424690 | C | T | 1 | a0001c0001t0007g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1043+32217C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68424690 | |||||||
chr9:68424970 | T | TCA | 9 | a0001c0001t0004g0154 a0001c0001t0014g0094 a0001c0002t0002g0003 others(6): Show |
9 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1043+32497_1043+32 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68424970 | |||||||
chr9:68425024 | T | C | 135 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(132): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1043+32551T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68425024 | |||||||
chr9:68425152 | C | A | 1 | a0001c0003t0005g0007 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1043+32679C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68425152 | |||||||
chr9:68425254 | A | C | 101 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(98): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1043+32781A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68425254 | |||||||
chr9:68425481 | T | C | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+33008T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68425481 | |||||||
chr9:68425583 | G | C | 99 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1043+33110G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68425583 | |||||||
chr9:68425609 | A | G | 5 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(2): Show |
5 | HG02572.hp1 HG02622.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+33136A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68425609 | |||||||
chr9:68425674 | GT | G | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+33204delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68425674 | ||||||
chr9:68425676 | T | G | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+33203T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68425676 | |||||||
chr9:68425870 | T | C | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1043+33397T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68425870 | |||||||
chr9:68426202 | T | C | 23 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(20): Show |
23 | HG00323.hp2 HG01255.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1043+33729T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68426202 | |||||||
chr9:68426260 | TA | T | 148 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(145): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1043+33801delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68426260 | ||||||
chr9:68426470 | A | G | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1043+33997A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68426470 | |||||||
chr9:68426473 | T | C | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043+34000T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68426473 | |||||||
chr9:68426516 | T | A | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1043+34043T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68426516 | |||||||
chr9:68426613 | A | AT | 10 | a0001c0001t0001g0093 a0001c0001t0001g0140 a0001c0001t0001g0174 others(7): Show |
10 | HG00673.hp2 HG01255.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1043+34155dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68426613 | ||||||
chr9:68426613 | AT | A | 13 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(10): Show |
13 | HG02109.hp1 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1043+34155delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68426613 | ||||||
chr9:68426613 | ATT | A | 7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(4): Show |
7 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1043+34154_1043+34 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68426613 | ||||||
chr9:68426616 | T | A | 21 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(18): Show |
21 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1043+34143T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68426616 | |||||||
chr9:68426682 | T | C | 1 | a0001c0001t0004g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1043+34209T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68426682 | |||||||
chr9:68426765 | C | CCAAGA | 18 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1043+34292_1043+34 others(11): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68426765 | |||||||
chr9:68426962 | A | G | 138 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(135): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1043+34489A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68426962 | |||||||
chr9:68427302 | C | G | 4 | a0001c0001t0001g0164 a0001c0001t0005g0137 a0001c0001t0005g0159 others(1): Show |
4 | NA18944.hp2 NA19004.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1043+34829C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68427302 | |||||||
chr9:68427347 | C | A | 4 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0015g0097 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043+34874C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68427347 | |||||||
chr9:68427508 | A | G | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1043+35035A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68427508 | |||||||
chr9:68427543 | G | C | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043+35070G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68427543 | |||||||
chr9:68427746 | T | C | 1 | a0001c0001t0003g0197 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1043+35273T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68427746 | |||||||
chr9:68427970 | G | A | 3 | a0001c0002t0002g0056 a0001c0002t0013g0045 a0001c0002t0013g0046 |
3 | HG00735.hp1 HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1043+35497G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68427970 | |||||||
chr9:68427980 | T | C | 2 | a0001c0001t0006g0075 a0001c0001t0006g0076 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1043+35507T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68427980 | |||||||
chr9:68428075 | T | G | 2 | a0001c0005t0009g0208 a0001c0005t0009g0210 |
2 | HG01255.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1043+35602T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68428075 | |||||||
chr9:68428096 | C | T | 23 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(20): Show |
23 | HG00323.hp2 HG01255.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1043+35623C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68428096 | |||||||
chr9:68428132 | A | C | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1043+35659A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68428132 | |||||||
chr9:68428286 | C | T | 133 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(130): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1043+35813C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68428286 | |||||||
chr9:68428332 | G | T | 1 | a0001c0001t0002g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1043+35859G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68428332 | |||||||
chr9:68428333 | C | A | 1 | a0001c0001t0002g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1043+35860C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68428333 | |||||||
chr9:68428849 | C | T | 133 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(130): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1044-36244C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68428849 | |||||||
chr9:68428935 | T | G | 1 | a0001c0002t0013g0046 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1044-36158T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68428935 | |||||||
chr9:68428973 | C | T | 133 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(130): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1044-36120C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68428973 | |||||||
chr9:68429033 | A | G | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-36060A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68429033 | |||||||
chr9:68429055 | C | G | 1 | a0001c0004t0002g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1044-36038C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68429055 | |||||||
chr9:68429156 | G | A | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1044-35937G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68429156 | |||||||
chr9:68429205 | G | A | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-35888G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68429205 | |||||||
chr9:68429210 | T | C | 134 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(131): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1044-35883T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68429210 | |||||||
chr9:68429432 | A | G | 1 | a0001c0003t0005g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1044-35661A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68429432 | |||||||
chr9:68429473 | T | C | 18 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1044-35620T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68429473 | |||||||
chr9:68429610 | TA | T | 100 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(97): Show |
100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1044-35480delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68429610 | ||||||
chr9:68429974 | G | A | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-35119G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68429974 | |||||||
chr9:68429979 | A | G | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1044-35114A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68429979 | |||||||
chr9:68430423 | T | C | 99 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(96): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.1044-34670T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68430423 | |||||||
chr9:68430508 | T | C | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1044-34585T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68430508 | |||||||
chr9:68430579 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1044-34514A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68430579 | |||||||
chr9:68430606 | G | A | 24 | a0001c0001t0002g0070 a0001c0001t0004g0085 a0001c0001t0004g0103 others(21): Show |
24 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1044-34487G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68430606 | |||||||
chr9:68430815 | T | C | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1044-34278T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68430815 | |||||||
chr9:68430871 | T | G | 1 | a0001c0003t0005g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1044-34222T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68430871 | |||||||
chr9:68430884 | G | C | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-34209G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68430884 | |||||||
chr9:68430905 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-34188A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68430905 | |||||||
chr9:68431042 | G | C | 133 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(130): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1044-34051G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68431042 | |||||||
chr9:68431126 | C | T | 1 | a0001c0002t0002g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1044-33967C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68431126 | |||||||
chr9:68431371 | A | C | 8 | a0001c0001t0001g0162 a0001c0001t0001g0179 a0001c0001t0001g0180 others(5): Show |
8 | HG00140.hp2 HG00735.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1044-33722A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68431371 | |||||||
chr9:68431454 | A | G | 111 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1044-33639A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68431454 | |||||||
chr9:68431667 | A | C | 106 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(103): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1044-33426A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68431667 | |||||||
chr9:68431820 | A | G | 1 | a0001c0019t0006g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1044-33273A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68431820 | |||||||
chr9:68431928 | G | A | 5 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0005t0009g0208 others(2): Show |
5 | HG01255.hp2 HG01891.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044-33165G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68431928 | |||||||
chr9:68432029 | C | T | 2 | a0001c0001t0007g0232 a0001c0006t0004g0107 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1044-33064C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68432029 | |||||||
chr9:68432078 | T | TA | 6 | a0001c0001t0020g0156 a0001c0001t0020g0157 a0001c0002t0001g0155 others(3): Show |
6 | HG00642.hp1 HG01081.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044-33008dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68432078 | ||||||
chr9:68432079 | A | T | 3 | a0001c0001t0010g0216 a0001c0001t0010g0217 a0001c0001t0011g0212 |
3 | HG02027.hp1 NA18980.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1044-33014A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68432079 | |||||||
chr9:68432119 | G | A | 1 | a0001c0011t0002g0033 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1044-32974G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68432119 | |||||||
chr9:68432128 | C | A | 1 | a0001c0004t0024g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1044-32965C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68432128 | |||||||
chr9:68432205 | A | AT | 6 | a0001c0001t0020g0156 a0001c0001t0020g0157 a0001c0002t0001g0155 others(3): Show |
6 | HG00642.hp1 HG01081.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044-32876dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68432205 | ||||||
chr9:68432218 | G | C | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-32875G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68432218 | |||||||
chr9:68432326 | A | G | 1 | a0005c0015t0012g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1044-32767A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68432326 | |||||||
chr9:68432527 | C | T | 5 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0005t0009g0208 others(2): Show |
5 | HG01255.hp2 HG01891.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044-32566C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68432527 | |||||||
chr9:68432630 | G | A | 24 | a0001c0001t0001g0110 a0001c0001t0001g0176 a0001c0001t0001g0181 others(21): Show |
24 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1044-32463G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68432630 | |||||||
chr9:68432717 | T | C | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-32376T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68432717 | |||||||
chr9:68432950 | AC | A | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-32141delC | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68432950 | ||||||
chr9:68433166 | C | T | 15 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(12): Show |
15 | HG00323.hp2 HG02109.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1044-31927C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68433166 | |||||||
chr9:68433325 | T | G | 9 | a0001c0001t0004g0154 a0001c0001t0014g0094 a0001c0002t0002g0003 others(6): Show |
9 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1044-31768T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68433325 | |||||||
chr9:68433416 | T | C | 1 | a0001c0001t0005g0161 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1044-31677T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68433416 | |||||||
chr9:68433629 | T | C | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1044-31464T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68433629 | |||||||
chr9:68433746 | T | C | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1044-31347T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68433746 | |||||||
chr9:68434007 | C | T | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1044-31086C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434007 | |||||||
chr9:68434151 | T | C | 9 | a0001c0001t0004g0151 a0001c0001t0020g0156 a0001c0001t0020g0157 others(6): Show |
9 | HG00642.hp1 HG01081.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1044-30942T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434151 | |||||||
chr9:68434171 | G | A | 18 | a0001c0001t0002g0005 a0001c0001t0009g0211 a0001c0001t0010g0220 others(15): Show |
18 | HG00423.hp2 HG01261.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.1044-30922G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434171 | |||||||
chr9:68434187 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1044-30906G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434187 | |||||||
chr9:68434200 | C | T | 1 | a0001c0001t0011g0219 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1044-30893C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434200 | |||||||
chr9:68434316 | CA | C | 26 | a0001c0001t0001g0145 a0001c0001t0002g0005 a0001c0001t0004g0151 others(23): Show |
26 | HG00280.hp2 HG00423.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.1044-30754delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68434316 | ||||||
chr9:68434316 | CAA | C | 7 | a0001c0001t0001g0100 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
7 | HG00673.hp1 HG01243.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1044-30755_1044-30 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68434316 | ||||||
chr9:68434316 | CAAA | C | 91 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0102 others(88): Show |
91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.1044-30756_1044-30 others(9): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68434316 | ||||||
chr9:68434316 | CAAAAAAA others(15): Show |
C | 20 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(17): Show |
20 | HG00323.hp2 HG01175.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1044-30775_1044-30 others(28): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68434316 | ||||||
chr9:68434335 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-30758A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434335 | |||||||
chr9:68434634 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0003g0203 |
2 | HG01261.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1044-30459C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434634 | |||||||
chr9:68434754 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-30339C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434754 | |||||||
chr9:68434822 | G | T | 6 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0139 others(3): Show |
6 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044-30271G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434822 | |||||||
chr9:68434842 | A | T | 60 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(57): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1044-30251A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434842 | |||||||
chr9:68434921 | G | A | 1 | a0001c0001t0003g0205 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1044-30172G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68434921 | |||||||
chr9:68435303 | A | G | 95 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(92): Show |
95 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1044-29790A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68435303 | |||||||
chr9:68435477 | A | C | 7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(4): Show |
7 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1044-29616A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68435477 | |||||||
chr9:68435519 | A | G | 7 | a0001c0001t0001g0177 a0001c0001t0011g0215 a0001c0002t0002g0036 others(4): Show |
7 | HG02056.hp2 HG02080.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.1044-29574A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68435519 | |||||||
chr9:68436177 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1044-28916G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68436177 | |||||||
chr9:68436234 | C | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0200 |
2 | HG01496.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1044-28859C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68436234 | |||||||
chr9:68436340 | T | C | 4 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0005t0009g0208 others(1): Show |
4 | HG01255.hp2 HG01891.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044-28753T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68436340 | |||||||
chr9:68436451 | A | G | 88 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(85): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1044-28642A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68436451 | |||||||
chr9:68436468 | G | A | 1 | a0001c0003t0005g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1044-28625G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68436468 | |||||||
chr9:68436487 | G | T | 4 | a0001c0003t0005g0007 a0001c0003t0005g0012 a0001c0003t0005g0013 others(1): Show |
4 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-28606G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68436487 | |||||||
chr9:68436515 | A | G | 4 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0005t0009g0208 others(1): Show |
4 | HG01255.hp2 HG01891.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044-28578A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68436515 | |||||||
chr9:68436635 | G | A | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-28458G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68436635 | |||||||
chr9:68436819 | G | A | 1 | a0001c0002t0002g0068 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1044-28274G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68436819 | |||||||
chr9:68436960 | T | C | 1 | a0001c0001t0018g0227 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1044-28133T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68436960 | |||||||
chr9:68437030 | C | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-28063C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68437030 | |||||||
chr9:68437031 | A | G | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-28062A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68437031 | |||||||
chr9:68437126 | A | G | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-27967A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68437126 | |||||||
chr9:68437352 | C | T | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1044-27741C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68437352 | |||||||
chr9:68437577 | TCA | T | 3 | a0001c0003t0001g0011 a0001c0003t0001g0017 a0001c0003t0001g0019 |
3 | NA18963.hp2 NA19056.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1044-27494_1044-27 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68437577 | ||||||
chr9:68437599 | ACT | A | 29 | a0001c0001t0002g0005 a0001c0001t0004g0151 a0001c0001t0005g0141 others(26): Show |
29 | HG00423.hp2 HG01175.hp1 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.1044-27490_1044-27 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68437599 | ||||||
chr9:68437601 | T | A | 25 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(22): Show |
25 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1044-27492T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68437601 | |||||||
chr9:68437640 | C | A | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-27453C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68437640 | |||||||
chr9:68437706 | T | C | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-27387T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68437706 | |||||||
chr9:68437763 | A | G | 45 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0103 others(42): Show |
45 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1044-27330A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68437763 | |||||||
chr9:68437846 | G | A | 20 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(17): Show |
20 | HG00423.hp2 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1044-27247G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68437846 | |||||||
chr9:68437923 | C | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-27170C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68437923 | |||||||
chr9:68438014 | G | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-27079G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68438014 | |||||||
chr9:68438054 | G | A | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1044-27039G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68438054 | |||||||
chr9:68438060 | G | T | 1 | a0001c0002t0002g0055 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1044-27033G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68438060 | |||||||
chr9:68438237 | C | T | 1 | a0001c0006t0001g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1044-26856C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68438237 | |||||||
chr9:68438276 | G | C | 20 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(17): Show |
20 | HG00423.hp2 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1044-26817G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68438276 | |||||||
chr9:68438286 | C | CA | 29 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0110 others(26): Show |
29 | HG00408.hp1 HG00438.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1044-26780dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68438286 | ||||||
chr9:68438286 | C | CAAAAA | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-26784_1044-26 others(11): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68438286 | ||||||
chr9:68438286 | CA | C | 23 | a0001c0001t0001g0099 a0001c0001t0001g0148 a0001c0001t0001g0173 others(20): Show |
23 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.1044-26780delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68438286 | ||||||
chr9:68438286 | CAA | C | 16 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1044-26781_1044-26 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68438286 | ||||||
chr9:68438335 | G | A | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-26758G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68438335 | |||||||
chr9:68438966 | G | A | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-26127G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68438966 | |||||||
chr9:68439266 | G | A | 6 | a0001c0001t0020g0156 a0001c0001t0020g0157 a0001c0001t0028g0040 others(3): Show |
6 | HG00642.hp1 HG01081.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044-25827G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68439266 | |||||||
chr9:68439515 | G | GTATATAT others(6): Show |
5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-25567_1044-25 others(19): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68439515 | ||||||
chr9:68439644 | A | T | 24 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(21): Show |
24 | HG00423.hp2 HG01261.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.1044-25449A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68439644 | |||||||
chr9:68439692 | C | CAT | 6 | a0001c0001t0020g0156 a0001c0001t0020g0157 a0001c0002t0001g0155 others(3): Show |
6 | HG00642.hp1 HG01081.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044-25387_1044-25 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68439692 | ||||||
chr9:68439694 | T | C | 4 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0005t0009g0208 others(1): Show |
4 | HG01255.hp2 HG01891.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044-25399T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68439694 | |||||||
chr9:68439706 | T | C | 1 | a0001c0001t0007g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1044-25387T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68439706 | |||||||
chr9:68439716 | C | CAT | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1044-25365_1044-25 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68439716 | ||||||
chr9:68439716 | C | T | 4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-25377C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68439716 | |||||||
chr9:68439718 | T | C | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-25375T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68439718 | |||||||
chr9:68439753 | G | A | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-25340G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68439753 | |||||||
chr9:68439880 | T | C | 2 | a0001c0001t0005g0159 a0001c0001t0005g0161 |
2 | NA19009.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1044-25213T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68439880 | |||||||
chr9:68440369 | A | C | 1 | a0001c0001t0004g0103 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1044-24724A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68440369 | |||||||
chr9:68440466 | A | G | 6 | a0001c0001t0010g0220 a0001c0001t0010g0224 a0001c0001t0012g0118 others(3): Show |
6 | HG02698.hp2 HG03490.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044-24627A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68440466 | |||||||
chr9:68440512 | T | C | 46 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0103 others(43): Show |
46 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1044-24581T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68440512 | |||||||
chr9:68440979 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0173 |
3 | HG02129.hp1 NA18612.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1044-24114T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68440979 | |||||||
chr9:68440980 | G | A | 151 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(148): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.1044-24113G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68440980 | |||||||
chr9:68440980 | G | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0173 |
3 | HG02129.hp1 NA18612.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1044-24113G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68440980 | |||||||
chr9:68441154 | T | C | 6 | a0001c0001t0020g0156 a0001c0001t0020g0157 a0001c0001t0028g0040 others(3): Show |
6 | HG00642.hp1 HG01081.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044-23939T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68441154 | |||||||
chr9:68441236 | A | G | 4 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0005t0009g0208 others(1): Show |
4 | HG01255.hp2 HG01891.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044-23857A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68441236 | |||||||
chr9:68441237 | T | A | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1044-23856T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68441237 | |||||||
chr9:68441734 | C | A | 1 | a0001c0001t0003g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1044-23359C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68441734 | |||||||
chr9:68441861 | C | T | 1 | a0001c0003t0001g0006 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1044-23232C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68441861 | |||||||
chr9:68441866 | A | G | 1 | a0001c0001t0004g0178 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1044-23227A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68441866 | |||||||
chr9:68441867 | C | CAAAG | 55 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0103 others(52): Show |
55 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1044-23225_1044-23 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68441867 | ||||||
chr9:68441973 | G | T | 1 | a0001c0001t0003g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1044-23120G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68441973 | |||||||
chr9:68442023 | C | T | 20 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(17): Show |
20 | HG00423.hp2 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1044-23070C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68442023 | |||||||
chr9:68442292 | CT | C | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-22792delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68442292 | ||||||
chr9:68442351 | G | C | 191 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(188): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.1044-22742G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68442351 | |||||||
chr9:68442454 | G | T | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-22639G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68442454 | |||||||
chr9:68442533 | G | A | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-22560G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68442533 | |||||||
chr9:68443128 | A | G | 3 | a0001c0001t0003g0195 a0001c0001t0003g0196 a0001c0002t0002g0053 |
3 | HG00642.hp2 HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1044-21965A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68443128 | |||||||
chr9:68443175 | G | A | 1 | a0001c0002t0002g0030 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1044-21918G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68443175 | |||||||
chr9:68443245 | G | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-21848G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68443245 | |||||||
chr9:68443275 | A | G | 226 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(223): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1044-21818A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68443275 | |||||||
chr9:68443296 | A | G | 1 | a0001c0003t0005g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1044-21797A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68443296 | |||||||
chr9:68443524 | T | C | 35 | a0001c0001t0002g0005 a0001c0001t0004g0103 a0001c0001t0004g0104 others(32): Show |
35 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1044-21569T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68443524 | |||||||
chr9:68443848 | C | T | 1 | a0001c0001t0012g0231 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1044-21245C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68443848 | |||||||
chr9:68444062 | C | CT | 5 | a0001c0001t0001g0198 a0001c0001t0020g0156 a0001c0001t0020g0157 others(2): Show |
5 | HG00423.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-21015dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68444062 | ||||||
chr9:68444105 | G | A | 1 | a0001c0001t0012g0187 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1044-20988G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68444105 | |||||||
chr9:68444455 | C | A | 28 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0006g0008 others(25): Show |
28 | HG00423.hp2 HG01175.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.1044-20638C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68444455 | |||||||
chr9:68444614 | ATGAGTTG others(18): Show |
A | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-20476_1044-20 others(31): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68444614 | ||||||
chr9:68444762 | G | T | 12 | a0001c0001t0002g0073 a0001c0001t0002g0080 a0001c0001t0004g0178 others(9): Show |
12 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1044-20331G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68444762 | |||||||
chr9:68444815 | A | G | 1 | a0001c0002t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1044-20278A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68444815 | |||||||
chr9:68444833 | A | T | 10 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(7): Show |
10 | HG01175.hp1 HG01255.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1044-20260A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68444833 | |||||||
chr9:68444973 | T | C | 20 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(17): Show |
20 | HG00423.hp2 HG01261.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.1044-20120T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68444973 | |||||||
chr9:68445027 | T | G | 7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(4): Show |
7 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1044-20066T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68445027 | |||||||
chr9:68445134 | AT | A | 33 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(30): Show |
33 | HG00323.hp2 HG01175.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.1044-19949delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68445134 | ||||||
chr9:68445210 | G | GA | 6 | a0001c0001t0001g0198 a0001c0001t0006g0008 a0001c0001t0007g0233 others(3): Show |
6 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044-19874dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68445210 | ||||||
chr9:68445441 | C | T | 1 | a0001c0004t0002g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1044-19652C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68445441 | |||||||
chr9:68445686 | G | A | 1 | a0001c0002t0002g0055 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1044-19407G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68445686 | |||||||
chr9:68445726 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1044-19367T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68445726 | |||||||
chr9:68445781 | T | C | 156 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(153): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1044-19312T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68445781 | |||||||
chr9:68445882 | G | A | 1 | a0001c0002t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1044-19211G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68445882 | |||||||
chr9:68446059 | A | C | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-19034A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68446059 | |||||||
chr9:68446116 | C | T | 1 | a0001c0001t0005g0149 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1044-18977C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68446116 | |||||||
chr9:68446162 | C | T | 3 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0082 |
3 | HG00323.hp1 HG02145.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1044-18931C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68446162 | |||||||
chr9:68446287 | A | G | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1044-18806A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68446287 | |||||||
chr9:68446326 | T | G | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-18767T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68446326 | |||||||
chr9:68446598 | G | A | 4 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0005t0009g0208 others(1): Show |
4 | HG01255.hp2 HG01891.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044-18495G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68446598 | |||||||
chr9:68446975 | G | A | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-18118G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68446975 | |||||||
chr9:68447042 | G | A | 2 | a0001c0001t0003g0166 a0001c0001t0028g0040 |
2 | HG02559.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1044-18051G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68447042 | |||||||
chr9:68447101 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1044-17992C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68447101 | |||||||
chr9:68447168 | G | A | 65 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(62): Show |
65 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1044-17925G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68447168 | |||||||
chr9:68447205 | C | G | 3 | a0001c0001t0020g0156 a0001c0001t0020g0157 a0001c0002t0001g0155 |
3 | HG02109.hp2 HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1044-17888C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68447205 | |||||||
chr9:68447471 | G | A | 1 | a0001c0002t0008g0025 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1044-17622G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68447471 | |||||||
chr9:68447480 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1044-17613C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68447480 | |||||||
chr9:68447564 | G | C | 28 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0006g0008 others(25): Show |
28 | HG00423.hp2 HG01175.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.1044-17529G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68447564 | |||||||
chr9:68447638 | A | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1044-17455A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68447638 | |||||||
chr9:68447704 | CT | C | 5 | a0001c0001t0001g0100 a0001c0001t0001g0139 a0001c0001t0001g0200 others(2): Show |
5 | HG01243.hp2 HG01496.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044-17384delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68447704 | ||||||
chr9:68448153 | C | T | 9 | a0001c0001t0004g0154 a0001c0001t0014g0094 a0001c0002t0002g0003 others(6): Show |
9 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1044-16940C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68448153 | |||||||
chr9:68448232 | G | A | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-16861G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68448232 | |||||||
chr9:68448263 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1044-16830C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68448263 | |||||||
chr9:68448321 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1044-16772C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68448321 | |||||||
chr9:68448509 | T | C | 1 | a0001c0002t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1044-16584T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68448509 | |||||||
chr9:68448661 | T | C | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-16432T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68448661 | |||||||
chr9:68448899 | G | A | 2 | a0001c0005t0009g0208 a0001c0005t0009g0210 |
2 | HG01255.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1044-16194G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68448899 | |||||||
chr9:68448953 | G | A | 1 | a0001c0001t0008g0081 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1044-16140G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68448953 | |||||||
chr9:68449111 | C | T | 28 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(25): Show |
28 | HG00323.hp2 HG01175.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1044-15982C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68449111 | |||||||
chr9:68449223 | G | T | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-15870G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68449223 | |||||||
chr9:68449330 | C | T | 1 | a0001c0002t0002g0015 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1044-15763C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68449330 | |||||||
chr9:68449393 | T | C | 1 | a0001c0001t0012g0187 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1044-15700T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68449393 | |||||||
chr9:68449426 | A | T | 3 | a0001c0001t0007g0165 a0001c0001t0007g0169 a0001c0001t0007g0171 |
3 | HG02630.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1044-15667A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68449426 | |||||||
chr9:68449968 | G | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1044-15125G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68449968 | |||||||
chr9:68450279 | CA | C | 36 | a0001c0001t0002g0005 a0001c0001t0004g0151 a0001c0001t0005g0141 others(33): Show |
36 | HG00423.hp2 HG01175.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.1044-14807delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68450279 | ||||||
chr9:68450585 | G | A | 22 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(19): Show |
22 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1044-14508G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68450585 | |||||||
chr9:68450672 | A | T | 5 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(2): Show |
5 | HG01433.hp1 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044-14421A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68450672 | |||||||
chr9:68450675 | C | T | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1044-14418C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68450675 | |||||||
chr9:68450809 | A | T | 2 | a0001c0001t0007g0233 a0004c0018t0006g0237 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1044-14284A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68450809 | |||||||
chr9:68450903 | A | G | 1 | a0001c0002t0002g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1044-14190A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68450903 | |||||||
chr9:68451249 | C | T | 56 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0103 others(53): Show |
56 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1044-13844C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68451249 | |||||||
chr9:68451285 | C | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-13808C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68451285 | |||||||
chr9:68451706 | G | A | 1 | a0001c0001t0011g0213 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1044-13387G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68451706 | |||||||
chr9:68451892 | C | T | 7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(4): Show |
7 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1044-13201C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68451892 | |||||||
chr9:68451894 | A | G | 18 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1044-13199A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68451894 | |||||||
chr9:68451915 | C | T | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1044-13178C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68451915 | |||||||
chr9:68452361 | C | T | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1044-12732C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68452361 | |||||||
chr9:68452370 | A | G | 193 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(190): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1044-12723A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68452370 | |||||||
chr9:68452398 | G | C | 18 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(15): Show |
18 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1044-12695G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68452398 | |||||||
chr9:68452599 | C | T | 1 | a0001c0001t0006g0079 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1044-12494C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68452599 | |||||||
chr9:68452667 | A | G | 4 | a0001c0001t0019g0001 a0001c0001t0019g0002 a0001c0005t0009g0208 others(1): Show |
4 | HG01255.hp2 HG01891.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044-12426A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68452667 | |||||||
chr9:68452693 | G | A | 2 | a0001c0001t0002g0070 a0001c0001t0009g0119 |
2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1044-12400G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68452693 | |||||||
chr9:68452886 | A | G | 88 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(85): Show |
88 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1044-12207A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68452886 | |||||||
chr9:68452929 | A | G | 5 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0004t0024g0240 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044-12164A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68452929 | |||||||
chr9:68453112 | A | G | 2 | a0001c0001t0001g0177 a0001c0002t0002g0062 |
2 | HG02523.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1044-11981A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68453112 | |||||||
chr9:68453299 | G | A | 2 | a0001c0001t0011g0215 a0001c0002t0002g0049 |
2 | HG02080.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1044-11794G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68453299 | |||||||
chr9:68453317 | G | A | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-11776G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68453317 | |||||||
chr9:68453403 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1044-11690A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68453403 | |||||||
chr9:68453463 | C | T | 2 | a0001c0005t0009g0208 a0001c0005t0009g0210 |
2 | HG01255.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1044-11630C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68453463 | |||||||
chr9:68453615 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1044-11478G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68453615 | |||||||
chr9:68453707 | G | T | 6 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(3): Show |
6 | HG01175.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044-11386G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68453707 | |||||||
chr9:68454263 | A | G | 1 | a0001c0002t0023g0061 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1044-10830A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68454263 | |||||||
chr9:68454386 | T | C | 2 | a0001c0001t0007g0167 a0001c0017t0004g0069 |
2 | HG00597.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1044-10707T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68454386 | |||||||
chr9:68454387 | G | T | 2 | a0001c0001t0007g0167 a0001c0017t0004g0069 |
2 | HG00597.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1044-10706G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68454387 | |||||||
chr9:68454412 | G | A | 2 | a0001c0005t0009g0208 a0001c0005t0009g0210 |
2 | HG01255.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1044-10681G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68454412 | |||||||
chr9:68454491 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0173 |
3 | HG02129.hp1 NA18612.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1044-10602T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68454491 | |||||||
chr9:68454631 | A | G | 1 | a0001c0003t0005g0007 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1044-10462A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68454631 | |||||||
chr9:68454715 | G | A | 4 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0004t0025g0236 others(1): Show |
4 | HG01175.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-10378G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68454715 | |||||||
chr9:68454869 | C | T | 63 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(60): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1044-10224C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68454869 | |||||||
chr9:68454878 | C | T | 1 | a0001c0001t0007g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1044-10215C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68454878 | |||||||
chr9:68454919 | C | A | 58 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(55): Show |
58 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.1044-10174C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68454919 | |||||||
chr9:68455337 | A | C | 4 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0004t0025g0236 others(1): Show |
4 | HG01175.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-9756A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68455337 | |||||||
chr9:68455456 | G | T | 1 | a0001c0002t0002g0066 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1044-9637G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68455456 | |||||||
chr9:68455505 | T | TA | 16 | a0001c0001t0001g0140 a0001c0001t0004g0103 a0001c0001t0004g0104 others(13): Show |
16 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1044-9573dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68455505 | ||||||
chr9:68455505 | T | TAA | 62 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(59): Show |
62 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1044-9574_1044-957 others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68455505 | ||||||
chr9:68455654 | G | A | 6 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(3): Show |
6 | HG01106.hp1 HG01175.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1044-9439G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68455654 | |||||||
chr9:68455689 | T | C | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1044-9404T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68455689 | |||||||
chr9:68455734 | G | T | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-9359G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68455734 | |||||||
chr9:68455898 | A | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-9195A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68455898 | |||||||
chr9:68455905 | A | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-9188A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68455905 | |||||||
chr9:68456095 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1044-8998C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456095 | |||||||
chr9:68456184 | A | G | 1 | a0001c0001t0002g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1044-8909A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456184 | |||||||
chr9:68456357 | C | T | 1 | a0001c0001t0015g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1044-8736C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456357 | |||||||
chr9:68456379 | T | C | 19 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(16): Show |
19 | HG00609.hp1 HG00639.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.1044-8714T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456379 | |||||||
chr9:68456477 | A | AT | 83 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(80): Show |
83 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1044-8601dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68456477 | ||||||
chr9:68456477 | AT | A | 7 | a0001c0001t0003g0172 a0001c0001t0006g0008 a0001c0001t0007g0232 others(4): Show |
7 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1044-8601delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68456477 | ||||||
chr9:68456522 | C | G | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-8571C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456522 | |||||||
chr9:68456561 | C | T | 2 | a0001c0001t0017g0221 a0001c0001t0017g0222 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1044-8532C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456561 | |||||||
chr9:68456618 | C | CT | 17 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0162 others(14): Show |
17 | HG00438.hp2 HG01175.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1044-8455dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68456618 | ||||||
chr9:68456618 | C | T | 4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-8475C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456618 | |||||||
chr9:68456783 | C | A | 3 | a0001c0005t0009g0208 a0001c0005t0009g0210 a0001c0020t0030g0090 |
3 | HG01255.hp2 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1044-8310C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456783 | |||||||
chr9:68456788 | C | A | 1 | a0001c0002t0013g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1044-8305C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456788 | |||||||
chr9:68456816 | G | C | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1044-8277G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456816 | |||||||
chr9:68456817 | G | A | 1 | a0001c0002t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1044-8276G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456817 | |||||||
chr9:68456970 | C | G | 1 | a0001c0001t0001g0147 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1044-8123C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68456970 | |||||||
chr9:68457017 | A | G | 57 | a0001c0001t0001g0095 a0001c0001t0001g0199 a0001c0001t0002g0071 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1044-8076A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457017 | |||||||
chr9:68457093 | T | C | 2 | a0001c0003t0001g0011 a0001c0003t0001g0019 |
2 | NA18963.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1044-8000T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457093 | |||||||
chr9:68457340 | C | T | 1 | a0001c0005t0004g0089 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1044-7753C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457340 | |||||||
chr9:68457356 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1044-7737T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457356 | |||||||
chr9:68457396 | C | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0200 |
2 | HG01496.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1044-7697C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457396 | |||||||
chr9:68457803 | C | CG | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-7290_1044-728 others(5): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457803 | |||||||
chr9:68457804 | A | G | 234 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(231): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1044-7289A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457804 | |||||||
chr9:68457804 | A | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-7289A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457804 | |||||||
chr9:68457805 | T | G | 3 | a0001c0005t0009g0208 a0001c0005t0009g0210 a0001c0020t0030g0090 |
3 | HG01255.hp2 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1044-7288T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457805 | |||||||
chr9:68457844 | A | G | 19 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(16): Show |
19 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1044-7249A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457844 | |||||||
chr9:68457972 | C | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-7121C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68457972 | |||||||
chr9:68458013 | C | T | 4 | a0001c0001t0001g0110 a0001c0001t0003g0203 a0001c0001t0003g0204 others(1): Show |
4 | HG00099.hp1 HG01168.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-7080C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458013 | |||||||
chr9:68458068 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1044-7025G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458068 | |||||||
chr9:68458115 | T | G | 20 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(17): Show |
20 | HG00423.hp2 HG02109.hp2 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.1044-6978T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458115 | |||||||
chr9:68458121 | G | A | 2 | a0001c0001t0006g0075 a0001c0001t0006g0076 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1044-6972G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458121 | |||||||
chr9:68458122 | G | T | 1 | a0001c0001t0021g0134 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1044-6971G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458122 | |||||||
chr9:68458161 | T | A | 25 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0006g0008 others(22): Show |
25 | HG00423.hp2 HG01175.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1044-6932T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458161 | |||||||
chr9:68458181 | T | A | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-6912T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458181 | |||||||
chr9:68458195 | T | G | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1044-6898T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458195 | |||||||
chr9:68458385 | G | A | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1044-6708G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458385 | |||||||
chr9:68458637 | A | T | 5 | a0001c0001t0001g0095 a0001c0002t0002g0030 a0001c0002t0002g0031 others(2): Show |
5 | HG00438.hp1 NA18968.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-6456A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458637 | |||||||
chr9:68458640 | T | G | 5 | a0001c0001t0001g0095 a0001c0002t0002g0030 a0001c0002t0002g0031 others(2): Show |
5 | HG00438.hp1 NA18968.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-6453T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458640 | |||||||
chr9:68458642 | A | AGTTTAGA others(1): Show |
5 | a0001c0001t0001g0095 a0001c0002t0002g0030 a0001c0002t0002g0031 others(2): Show |
5 | HG00438.hp1 NA18968.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-6451_1044-645 others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458642 | |||||||
chr9:68458644 | A | T | 5 | a0001c0001t0001g0095 a0001c0002t0002g0030 a0001c0002t0002g0031 others(2): Show |
5 | HG00438.hp1 NA18968.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-6449A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458644 | |||||||
chr9:68458705 | G | C | 92 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(89): Show |
92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1044-6388G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68458705 | |||||||
chr9:68459379 | G | A | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1044-5714G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68459379 | |||||||
chr9:68459530 | T | G | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-5563T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68459530 | |||||||
chr9:68459741 | A | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-5352A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68459741 | |||||||
chr9:68459868 | T | TA | 6 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044-5217dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68459868 | ||||||
chr9:68459935 | C | T | 54 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0103 others(51): Show |
54 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1044-5158C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68459935 | |||||||
chr9:68460106 | A | T | 1 | a0001c0002t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1044-4987A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68460106 | |||||||
chr9:68460157 | G | T | 19 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(16): Show |
19 | HG00423.hp2 HG02109.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1044-4936G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68460157 | |||||||
chr9:68460540 | C | T | 9 | a0001c0001t0004g0154 a0001c0001t0014g0094 a0001c0002t0002g0003 others(6): Show |
9 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1044-4553C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68460540 | |||||||
chr9:68460662 | A | G | 1 | a0001c0003t0005g0007 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1044-4431A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68460662 | |||||||
chr9:68460683 | C | T | 1 | a0001c0001t0015g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1044-4410C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68460683 | |||||||
chr9:68460864 | T | A | 73 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(70): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1044-4229T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68460864 | |||||||
chr9:68460967 | G | A | 1 | a0001c0002t0008g0025 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1044-4126G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68460967 | |||||||
chr9:68460976 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-4117C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68460976 | |||||||
chr9:68461226 | C | T | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-3867C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68461226 | |||||||
chr9:68461285 | T | C | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1044-3808T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68461285 | |||||||
chr9:68461306 | G | C | 6 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044-3787G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68461306 | |||||||
chr9:68461637 | A | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-3456A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68461637 | |||||||
chr9:68461853 | G | C | 8 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(5): Show |
8 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1044-3240G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68461853 | |||||||
chr9:68462004 | A | G | 72 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(69): Show |
72 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1044-3089A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68462004 | |||||||
chr9:68462021 | T | C | 92 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(89): Show |
92 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1044-3072T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68462021 | |||||||
chr9:68462135 | GA | G | 31 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(28): Show |
31 | HG00323.hp2 HG01175.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.1044-2952delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68462135 | ||||||
chr9:68462421 | A | C | 22 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(19): Show |
22 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1044-2672A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68462421 | |||||||
chr9:68462442 | A | G | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1044-2651A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68462442 | |||||||
chr9:68462471 | A | G | 1 | a0001c0004t0002g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1044-2622A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68462471 | |||||||
chr9:68462546 | C | T | 4 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044-2547C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68462546 | |||||||
chr9:68462728 | C | T | 1 | a0001c0001t0007g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1044-2365C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68462728 | |||||||
chr9:68462729 | G | T | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1044-2364G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68462729 | |||||||
chr9:68462887 | G | A | 1 | a0001c0002t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1044-2206G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68462887 | |||||||
chr9:68463144 | G | A | 59 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(56): Show |
59 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1044-1949G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68463144 | |||||||
chr9:68463182 | GT | G | 12 | a0001c0001t0001g0115 a0001c0001t0004g0103 a0001c0001t0004g0104 others(9): Show |
12 | HG00323.hp2 HG01255.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.1044-1897delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68463182 | ||||||
chr9:68463183 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1044-1910T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68463183 | |||||||
chr9:68463206 | A | G | 27 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(24): Show |
27 | HG00323.hp2 HG01175.hp1 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1044-1887A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68463206 | |||||||
chr9:68463241 | G | A | 5 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-1852G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68463241 | |||||||
chr9:68463244 | G | A | 4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-1849G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68463244 | |||||||
chr9:68463293 | A | G | 1 | a0001c0001t0008g0078 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1044-1800A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68463293 | |||||||
chr9:68463308 | C | T | 1 | a0001c0005t0014g0088 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1044-1785C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68463308 | |||||||
chr9:68463770 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-1323A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68463770 | |||||||
chr9:68463800 | T | C | 14 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(11): Show |
14 | HG00323.hp2 HG01255.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1044-1293T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68463800 | |||||||
chr9:68464137 | G | C | 1 | a0001c0002t0002g0051 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1044-956G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68464137 | |||||||
chr9:68464152 | A | C | 2 | a0001c0001t0020g0156 a0001c0001t0020g0157 |
2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1044-941A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68464152 | |||||||
chr9:68464225 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1044-868C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68464225 | |||||||
chr9:68464280 | T | C | 5 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(2): Show |
5 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1044-813T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68464280 | |||||||
chr9:68464365 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1044-728A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68464365 | |||||||
chr9:68464569 | T | C | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1044-524T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68464569 | |||||||
chr9:68464583 | C | A | 17 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0006g0008 others(14): Show |
17 | HG01175.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.1044-510C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68464583 | |||||||
chr9:68464899 | T | C | 23 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(20): Show |
23 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1044-194T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | chr9 | 68464899 | |||||||
chr9:68465035 | GA | G | 54 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0103 others(51): Show |
54 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1044-49delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 68465035 | ||||||
chr9:68465385 | T | C | 1 | a0001c0001t0008g0081 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1159+177T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68465385 | |||||||
chr9:68465391 | T | G | 4 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+183T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68465391 | |||||||
chr9:68465610 | G | A | 4 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0004t0025g0236 others(1): Show |
4 | HG01175.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1159+402G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68465610 | |||||||
chr9:68465705 | G | A | 54 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0103 others(51): Show |
54 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1159+497G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68465705 | |||||||
chr9:68465809 | G | T | 6 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(3): Show |
6 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+601G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68465809 | |||||||
chr9:68465816 | G | A | 6 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(3): Show |
6 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+608G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68465816 | |||||||
chr9:68465929 | A | G | 91 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(88): Show |
91 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1159+721A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68465929 | |||||||
chr9:68465939 | A | T | 3 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 |
3 | HG03195.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1159+731A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68465939 | |||||||
chr9:68466260 | G | A | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1159+1052G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68466260 | |||||||
chr9:68466264 | C | CTGTG | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1159+1060_1159+106 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68466264 | ||||||
chr9:68466270 | GT | G | 8 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(5): Show |
8 | HG01255.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+1078delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68466270 | ||||||
chr9:68466271 | T | TG | 6 | a0001c0001t0006g0008 a0001c0001t0007g0233 a0001c0001t0015g0105 others(3): Show |
6 | HG01175.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159+1063_1159+106 others(5): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68466271 | |||||||
chr9:68466271 | T | TGTG | 8 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(5): Show |
8 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+1063_1159+106 others(7): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68466271 | |||||||
chr9:68466272 | T | G | 68 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(65): Show |
68 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1159+1064T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68466272 | |||||||
chr9:68466273 | T | G | 8 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(5): Show |
8 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+1065T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68466273 | |||||||
chr9:68466393 | T | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0004 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1159+1185T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68466393 | |||||||
chr9:68466606 | T | G | 1 | a0001c0002t0002g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1159+1398T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68466606 | |||||||
chr9:68466609 | G | C | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1159+1401G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68466609 | |||||||
chr9:68466952 | T | C | 3 | a0001c0001t0005g0117 a0001c0001t0005g0130 a0001c0001t0005g0149 |
3 | NA18952.hp1 NA18982.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1159+1744T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68466952 | |||||||
chr9:68466992 | T | C | 1 | a0001c0001t0003g0202 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1159+1784T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68466992 | |||||||
chr9:68467014 | G | A | 1 | a0001c0002t0002g0053 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1159+1806G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467014 | |||||||
chr9:68467099 | A | G | 55 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(52): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1159+1891A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467099 | |||||||
chr9:68467109 | G | A | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1159+1901G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467109 | |||||||
chr9:68467220 | C | A | 55 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(52): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1159+2012C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467220 | |||||||
chr9:68467241 | T | C | 82 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(79): Show |
82 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1159+2033T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467241 | |||||||
chr9:68467255 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1159+2047C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467255 | |||||||
chr9:68467458 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1159+2250C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467458 | |||||||
chr9:68467672 | G | A | 89 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(86): Show |
89 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1159+2464G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467672 | |||||||
chr9:68467687 | A | G | 25 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(22): Show |
25 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1159+2479A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467687 | |||||||
chr9:68467742 | T | C | 19 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(16): Show |
19 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1159+2534T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467742 | |||||||
chr9:68467766 | C | T | 55 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(52): Show |
55 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1159+2558C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467766 | |||||||
chr9:68467838 | T | TC | 28 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(25): Show |
28 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1159+2631dupC | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68467838 | ||||||
chr9:68467942 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1159+2734A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467942 | |||||||
chr9:68467951 | T | A | 1 | a0001c0002t0008g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1159+2743T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467951 | |||||||
chr9:68467961 | C | T | 25 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(22): Show |
25 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1159+2753C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68467961 | |||||||
chr9:68468004 | C | T | 54 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0103 others(51): Show |
54 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1159+2796C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468004 | |||||||
chr9:68468009 | A | AATCC | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1159+2802_1159+280 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68468009 | ||||||
chr9:68468014 | A | ACCCT | 23 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(20): Show |
23 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1159+2811_1159+281 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68468014 | ||||||
chr9:68468014 | A | T | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1159+2806A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468014 | |||||||
chr9:68468075 | T | G | 1 | a0001c0005t0014g0088 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1159+2867T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468075 | |||||||
chr9:68468169 | C | T | 4 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+2961C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468169 | |||||||
chr9:68468175 | T | C | 4 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+2967T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468175 | |||||||
chr9:68468176 | T | A | 4 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1159+2968T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468176 | |||||||
chr9:68468201 | A | AC | 23 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(20): Show |
23 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1159+2996dupC | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68468201 | ||||||
chr9:68468251 | G | A | 2 | a0001c0002t0002g0010 a0001c0002t0002g0068 |
2 | NA18963.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1159+3043G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468251 | |||||||
chr9:68468506 | C | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1159+3298C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468506 | |||||||
chr9:68468542 | A | G | 74 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(71): Show |
74 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1159+3334A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468542 | |||||||
chr9:68468651 | T | C | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1159+3443T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468651 | |||||||
chr9:68468725 | A | G | 1 | a0001c0001t0005g0158 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1159+3517A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468725 | |||||||
chr9:68468752 | G | C | 44 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0100 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.1159+3544G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468752 | |||||||
chr9:68468816 | T | C | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1159+3608T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468816 | |||||||
chr9:68468877 | T | G | 89 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(86): Show |
89 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1159+3669T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68468877 | |||||||
chr9:68469062 | G | A | 1 | a0001c0002t0008g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1159+3854G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469062 | |||||||
chr9:68469062 | G | T | 11 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(8): Show |
11 | HG00323.hp2 HG01255.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1159+3854G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469062 | |||||||
chr9:68469205 | G | A | 90 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(87): Show |
90 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1159+3997G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469205 | |||||||
chr9:68469360 | T | A | 2 | a0001c0001t0002g0070 a0001c0001t0009g0119 |
2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1159+4152T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469360 | |||||||
chr9:68469360 | TA | T | 60 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(57): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1159+4162delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68469360 | ||||||
chr9:68469361 | A | T | 4 | a0001c0001t0007g0168 a0001c0001t0010g0216 a0001c0001t0010g0217 others(1): Show |
4 | HG01346.hp2 HG02027.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1159+4153A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469361 | |||||||
chr9:68469371 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1159+4163T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469371 | |||||||
chr9:68469396 | A | G | 54 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(51): Show |
54 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1159+4188A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469396 | |||||||
chr9:68469446 | A | G | 3 | a0001c0001t0015g0097 a0001c0001t0019g0001 a0001c0001t0019g0002 |
3 | HG01891.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1159+4238A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469446 | |||||||
chr9:68469496 | T | C | 28 | a0001c0001t0002g0070 a0001c0001t0004g0103 a0001c0001t0004g0104 others(25): Show |
28 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1159+4288T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469496 | |||||||
chr9:68469626 | A | G | 9 | a0001c0001t0004g0151 a0001c0001t0015g0097 a0001c0001t0015g0116 others(6): Show |
9 | HG01255.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1159+4418A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469626 | |||||||
chr9:68469712 | C | G | 1 | a0001c0001t0012g0231 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1159+4504C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469712 | |||||||
chr9:68469740 | A | C | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1159+4532A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469740 | |||||||
chr9:68469754 | G | C | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1159+4546G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469754 | |||||||
chr9:68469942 | C | G | 2 | a0001c0001t0002g0070 a0001c0001t0009g0119 |
2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1159+4734C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469942 | |||||||
chr9:68469963 | T | A | 1 | a0001c0001t0002g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1159+4755T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68469963 | |||||||
chr9:68470315 | G | T | 1 | a0001c0001t0003g0196 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1159+5107G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68470315 | |||||||
chr9:68470991 | A | G | 1 | a0001c0006t0001g0092 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1159+5783A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68470991 | |||||||
chr9:68471081 | A | G | 2 | a0001c0002t0002g0043 a0001c0002t0002g0064 |
2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1159+5873A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68471081 | |||||||
chr9:68471517 | T | G | 94 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(91): Show |
94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1159+6309T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68471517 | |||||||
chr9:68471616 | T | TA | 6 | a0001c0001t0004g0085 a0001c0001t0007g0232 a0001c0001t0011g0212 others(3): Show |
6 | HG02647.hp1 HG02922.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1159+6425dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68471616 | ||||||
chr9:68471616 | TA | T | 9 | a0001c0001t0001g0174 a0001c0001t0002g0070 a0001c0001t0003g0202 others(6): Show |
9 | HG01169.hp1 HG02055.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.1159+6425delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68471616 | ||||||
chr9:68471632 | A | G | 1 | a0001c0001t0010g0220 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1159+6424A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68471632 | |||||||
chr9:68471654 | T | G | 2 | a0001c0001t0002g0070 a0001c0001t0009g0119 |
2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1159+6446T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68471654 | |||||||
chr9:68471882 | G | A | 7 | a0001c0001t0006g0008 a0001c0001t0007g0165 a0001c0001t0007g0169 others(4): Show |
7 | HG01175.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1159+6674G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68471882 | |||||||
chr9:68471918 | C | CA | 8 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(5): Show |
8 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1159+6719dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68471918 | ||||||
chr9:68471951 | T | C | 57 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(54): Show |
57 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1159+6743T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68471951 | |||||||
chr9:68471970 | C | CA | 69 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(66): Show |
69 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1159+6777dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68471970 | ||||||
chr9:68471970 | CA | C | 19 | a0001c0001t0001g0110 a0001c0001t0001g0176 a0001c0001t0001g0181 others(16): Show |
19 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1159+6777delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68471970 | ||||||
chr9:68471970 | CAAAAA | C | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1159+6773_1159+677 others(9): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68471970 | ||||||
chr9:68472085 | G | T | 2 | a0001c0005t0009g0208 a0001c0005t0009g0210 |
2 | HG01255.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1159+6877G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68472085 | |||||||
chr9:68472267 | A | G | 1 | a0001c0001t0002g0005 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1159+7059A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68472267 | |||||||
chr9:68472416 | T | TTAC | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1160-7002_1160-700 others(7): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68472416 | |||||||
chr9:68472419 | T | TTTGGGAG others(4): Show |
11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1160-6999_1160-699 others(15): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68472419 | |||||||
chr9:68472546 | G | T | 21 | a0001c0001t0002g0005 a0001c0001t0005g0141 a0001c0001t0009g0211 others(18): Show |
21 | HG00423.hp2 HG02109.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1160-6872G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68472546 | |||||||
chr9:68472814 | C | T | 4 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-6604C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68472814 | |||||||
chr9:68472823 | T | C | 50 | a0001c0001t0002g0005 a0001c0001t0002g0070 a0001c0001t0004g0103 others(47): Show |
50 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.1160-6595T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68472823 | |||||||
chr9:68473006 | C | CT | 9 | a0001c0001t0004g0154 a0001c0001t0014g0094 a0001c0002t0002g0003 others(6): Show |
9 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1160-6404dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68473006 | ||||||
chr9:68473198 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1160-6220A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68473198 | |||||||
chr9:68473219 | A | G | 94 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(91): Show |
94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1160-6199A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68473219 | |||||||
chr9:68473324 | C | T | 5 | a0001c0001t0007g0165 a0001c0001t0007g0169 a0001c0001t0007g0171 others(2): Show |
5 | HG02630.hp1 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160-6094C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68473324 | |||||||
chr9:68473351 | C | A | 1 | a0001c0001t0002g0073 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1160-6067C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68473351 | |||||||
chr9:68473397 | A | G | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1160-6021A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68473397 | |||||||
chr9:68473857 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1160-5561T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68473857 | |||||||
chr9:68473891 | C | G | 86 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(83): Show |
86 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1160-5527C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68473891 | |||||||
chr9:68473899 | C | A | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1160-5519C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68473899 | |||||||
chr9:68473977 | G | A | 84 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(81): Show |
84 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1160-5441G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68473977 | |||||||
chr9:68474064 | G | A | 1 | a0001c0002t0002g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1160-5354G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68474064 | |||||||
chr9:68474493 | A | T | 2 | a0001c0002t0002g0041 a0001c0002t0002g0042 |
2 | HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1160-4925A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68474493 | |||||||
chr9:68474631 | C | T | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1160-4787C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68474631 | |||||||
chr9:68474764 | G | C | 1 | a0001c0002t0002g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1160-4654G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68474764 | |||||||
chr9:68475184 | A | AT | 7 | a0001c0001t0001g0108 a0001c0001t0001g0183 a0001c0001t0001g0199 others(4): Show |
7 | HG00673.hp1 HG01978.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1160-4212dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68475184 | ||||||
chr9:68475184 | A | ATT | 10 | a0001c0001t0004g0154 a0001c0001t0014g0094 a0001c0001t0015g0105 others(7): Show |
10 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160-4213_1160-421 others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68475184 | ||||||
chr9:68475184 | A | ATTT | 16 | a0001c0001t0001g0099 a0001c0001t0001g0150 a0001c0001t0004g0151 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1160-4214_1160-421 others(7): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68475184 | ||||||
chr9:68475184 | A | ATTTT | 43 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0121 others(40): Show |
43 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1160-4215_1160-421 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68475184 | ||||||
chr9:68475184 | A | ATTTTT | 11 | a0001c0001t0001g0112 a0001c0001t0001g0128 a0001c0001t0001g0136 others(8): Show |
11 | HG00323.hp2 HG02056.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1160-4216_1160-421 others(9): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68475184 | ||||||
chr9:68475184 | AT | A | 6 | a0001c0001t0003g0192 a0001c0001t0004g0103 a0001c0001t0004g0104 others(3): Show |
6 | HG00597.hp1 HG00597.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-4212delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68475184 | ||||||
chr9:68475184 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0002g0070 a0001c0001t0009g0119 |
2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1160-4222_1160-421 others(15): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68475184 | ||||||
chr9:68475252 | C | T | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1160-4166C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68475252 | |||||||
chr9:68475304 | T | A | 2 | a0001c0002t0002g0043 a0001c0002t0002g0064 |
2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1160-4114T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68475304 | |||||||
chr9:68475375 | G | A | 87 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(84): Show |
87 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1160-4043G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68475375 | |||||||
chr9:68475382 | T | C | 60 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(57): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1160-4036T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68475382 | |||||||
chr9:68475588 | C | T | 3 | a0001c0001t0014g0094 a0003c0008t0026g0234 a0003c0008t0027g0235 |
3 | HG02109.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1160-3830C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68475588 | |||||||
chr9:68475662 | A | C | 14 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(11): Show |
14 | HG00323.hp2 HG01255.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1160-3756A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68475662 | |||||||
chr9:68476094 | A | G | 11 | a0001c0001t0002g0070 a0001c0001t0004g0154 a0001c0001t0009g0119 others(8): Show |
11 | HG02109.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1160-3324A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68476094 | |||||||
chr9:68476136 | T | C | 1 | a0001c0001t0015g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1160-3282T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68476136 | |||||||
chr9:68476310 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1160-3108T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68476310 | |||||||
chr9:68476870 | A | T | 2 | a0001c0001t0003g0204 a0001c0001t0003g0205 |
2 | HG00099.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1160-2548A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68476870 | |||||||
chr9:68476876 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1160-2542T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68476876 | |||||||
chr9:68476954 | G | C | 2 | a0001c0001t0009g0211 a0001c0001t0011g0213 |
2 | NA18612.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1160-2464G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68476954 | |||||||
chr9:68476984 | A | AT | 83 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(80): Show |
83 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1160-2424dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68476984 | ||||||
chr9:68477132 | G | A | 1 | a0001c0001t0004g0178 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1160-2286G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68477132 | |||||||
chr9:68477147 | C | G | 1 | a0001c0011t0002g0033 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1160-2271C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68477147 | |||||||
chr9:68477203 | A | G | 2 | a0001c0002t0002g0043 a0001c0002t0002g0064 |
2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1160-2215A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68477203 | |||||||
chr9:68477206 | G | A | 3 | a0001c0002t0002g0030 a0001c0002t0002g0038 a0001c0002t0002g0039 |
3 | NA18972.hp2 NA18982.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1160-2212G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68477206 | |||||||
chr9:68477256 | C | T | 1 | a0001c0001t0020g0156 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1160-2162C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68477256 | |||||||
chr9:68477319 | G | A | 60 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(57): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1160-2099G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68477319 | |||||||
chr9:68477333 | G | GA | 94 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(91): Show |
94 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1160-2078dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr9 | 68477333 | ||||||
chr9:68477474 | G | A | 2 | a0001c0005t0014g0087 a0001c0005t0014g0088 |
2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1160-1944G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68477474 | |||||||
chr9:68477592 | A | C | 9 | a0001c0001t0004g0151 a0001c0001t0015g0097 a0001c0001t0015g0116 others(6): Show |
9 | HG01255.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1160-1826A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68477592 | |||||||
chr9:68477948 | G | A | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1160-1470G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68477948 | |||||||
chr9:68478060 | C | T | 7 | a0001c0001t0006g0008 a0001c0001t0007g0165 a0001c0001t0007g0169 others(4): Show |
7 | HG01175.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1160-1358C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478060 | |||||||
chr9:68478207 | C | T | 2 | a0001c0002t0002g0043 a0001c0002t0002g0064 |
2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1160-1211C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478207 | |||||||
chr9:68478304 | A | G | 75 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(72): Show |
75 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1160-1114A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478304 | |||||||
chr9:68478613 | C | T | 7 | a0001c0001t0006g0008 a0001c0001t0007g0165 a0001c0001t0007g0169 others(4): Show |
7 | HG01175.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1160-805C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478613 | |||||||
chr9:68478630 | T | C | 62 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(59): Show |
62 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1160-788T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478630 | |||||||
chr9:68478644 | A | G | 5 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(2): Show |
5 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1160-774A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478644 | |||||||
chr9:68478751 | T | C | 85 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(82): Show |
85 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1160-667T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478751 | |||||||
chr9:68478863 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1160-555G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478863 | |||||||
chr9:68478866 | A | G | 1 | a0001c0001t0015g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1160-552A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478866 | |||||||
chr9:68478907 | A | G | 8 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(5): Show |
8 | HG00323.hp2 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1160-511A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478907 | |||||||
chr9:68478938 | A | G | 60 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(57): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1160-480A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478938 | |||||||
chr9:68478995 | C | T | 1 | a0005c0015t0012g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1160-423C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68478995 | |||||||
chr9:68479089 | A | G | 1 | a0001c0002t0008g0025 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1160-329A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68479089 | |||||||
chr9:68479292 | T | C | 69 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(66): Show |
69 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1160-126T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68479292 | |||||||
chr9:68479314 | C | T | 63 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(60): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1160-104C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 7/10 | chr9 | 68479314 | |||||||
chr9:68479571 | G | A | 7 | a0001c0001t0006g0008 a0001c0001t0007g0165 a0001c0001t0007g0169 others(4): Show |
7 | HG01175.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1295+18G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68479571 | |||||||
chr9:68479663 | G | A | 1 | a0001c0002t0008g0025 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1295+110G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68479663 | |||||||
chr9:68479672 | C | A | 1 | a0001c0001t0015g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1295+119C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68479672 | |||||||
chr9:68479717 | G | A | 2 | a0001c0005t0009g0208 a0001c0005t0009g0210 |
2 | HG01255.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1295+164G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68479717 | |||||||
chr9:68479866 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0102 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1295+313G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68479866 | |||||||
chr9:68479922 | C | CA | 11 | a0001c0001t0001g0145 a0001c0001t0003g0203 a0001c0001t0006g0008 others(8): Show |
11 | HG01261.hp1 HG02258.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1295+388dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 68479922 | ||||||
chr9:68479922 | CA | C | 5 | a0001c0001t0001g0128 a0001c0001t0005g0158 a0001c0002t0008g0034 others(2): Show |
5 | HG02451.hp2 HG02523.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.1295+388delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 68479922 | ||||||
chr9:68480076 | T | C | 2 | a0001c0001t0005g0141 a0001c0002t0008g0044 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1295+523T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68480076 | |||||||
chr9:68480159 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1295+606A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68480159 | |||||||
chr9:68480480 | G | A | 3 | a0001c0001t0002g0074 a0001c0001t0008g0078 a0001c0001t0008g0081 |
3 | HG00609.hp2 NA18941.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.1295+927G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68480480 | |||||||
chr9:68480698 | C | CA | 6 | a0001c0001t0001g0128 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
6 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295+1156dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 68480698 | ||||||
chr9:68480705 | A | C | 6 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0002t0013g0048 others(3): Show |
6 | HG01346.hp2 HG02572.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1295+1152A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68480705 | |||||||
chr9:68480715 | C | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0102 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1295+1162C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68480715 | |||||||
chr9:68480830 | T | C | 8 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(5): Show |
8 | HG00323.hp2 HG02257.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295+1277T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68480830 | |||||||
chr9:68480931 | C | T | 55 | a0001c0001t0001g0095 a0001c0001t0001g0199 a0001c0001t0002g0071 others(52): Show |
55 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1295+1378C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68480931 | |||||||
chr9:68481512 | G | A | 7 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(4): Show |
7 | HG00735.hp1 HG00741.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1295+1959G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68481512 | |||||||
chr9:68481531 | A | T | 7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(4): Show |
7 | HG00323.hp2 HG02257.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1295+1978A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68481531 | |||||||
chr9:68481804 | A | C | 2 | a0001c0001t0006g0075 a0001c0001t0006g0076 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1296-2061A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68481804 | |||||||
chr9:68481847 | G | A | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1296-2018G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68481847 | |||||||
chr9:68482095 | C | T | 5 | a0001c0001t0007g0165 a0001c0001t0007g0169 a0001c0001t0007g0171 others(2): Show |
5 | HG02630.hp1 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296-1770C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482095 | |||||||
chr9:68482188 | T | C | 1 | a0001c0005t0009g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1296-1677T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482188 | |||||||
chr9:68482192 | C | A | 1 | a0001c0003t0005g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1296-1673C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482192 | |||||||
chr9:68482202 | C | G | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1296-1663C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482202 | |||||||
chr9:68482573 | C | T | 1 | a0001c0001t0007g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1296-1292C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482573 | |||||||
chr9:68482655 | TCCTCCAA others(20): Show |
T | 1 | a0001c0002t0002g0068 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1296-1204_1296-117 others(31): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 68482655 | ||||||
chr9:68482784 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0184 |
2 | HG01175.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1296-1081T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482784 | |||||||
chr9:68482867 | C | A | 24 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0005g0141 others(21): Show |
24 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1296-998C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482867 | |||||||
chr9:68482890 | G | T | 1 | a0001c0011t0002g0033 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1296-975G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482890 | |||||||
chr9:68482900 | T | C | 1 | a0001c0001t0007g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1296-965T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482900 | |||||||
chr9:68482916 | T | C | 1 | a0001c0001t0007g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1296-949T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482916 | |||||||
chr9:68482926 | C | T | 30 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0005g0141 others(27): Show |
30 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1296-939C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68482926 | |||||||
chr9:68483001 | C | T | 2 | a0001c0001t0015g0105 a0004c0013t0001g0146 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1296-864C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483001 | |||||||
chr9:68483080 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1296-785T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483080 | |||||||
chr9:68483097 | T | C | 1 | a0001c0001t0005g0158 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1296-768T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483097 | |||||||
chr9:68483440 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1296-425C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483440 | |||||||
chr9:68483450 | C | G | 5 | a0001c0001t0011g0215 a0001c0002t0002g0036 a0001c0002t0002g0037 others(2): Show |
5 | HG02056.hp2 HG02080.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296-415C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483450 | |||||||
chr9:68483602 | G | T | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1296-263G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483602 | |||||||
chr9:68483655 | A | G | 2 | a0001c0001t0015g0105 a0004c0013t0001g0146 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1296-210A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483655 | |||||||
chr9:68483693 | C | T | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1296-172C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483693 | |||||||
chr9:68483694 | G | A | 7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(4): Show |
7 | HG00323.hp2 HG02257.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1296-171G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483694 | |||||||
chr9:68483700 | T | C | 7 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(4): Show |
7 | HG00323.hp2 HG02257.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1296-165T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483700 | |||||||
chr9:68483701 | G | A | 1 | a0004c0013t0001g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1296-164G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 8/10 | chr9 | 68483701 | |||||||
chr9:68484070 | C | T | 61 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(58): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1479+22C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68484070 | |||||||
chr9:68484071 | A | G | 79 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(76): Show |
79 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1479+23A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68484071 | |||||||
chr9:68484373 | C | CA | 11 | a0001c0001t0001g0179 a0001c0001t0003g0195 a0001c0001t0007g0167 others(8): Show |
11 | HG00597.hp1 HG00741.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1479+343dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484373 | ||||||
chr9:68484373 | CA | C | 18 | a0001c0001t0001g0099 a0001c0001t0001g0112 a0001c0001t0001g0163 others(15): Show |
18 | HG00280.hp1 HG01255.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1479+343delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484373 | ||||||
chr9:68484373 | CAA | C | 26 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0103 others(23): Show |
26 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1479+342_1479+343d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484373 | ||||||
chr9:68484389 | A | G | 1 | a0001c0001t0015g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1479+341A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68484389 | |||||||
chr9:68484439 | C | T | 6 | a0001c0001t0015g0097 a0001c0001t0015g0116 a0001c0001t0019g0001 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1479+391C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68484439 | |||||||
chr9:68484541 | A | AAC | 8 | a0001c0001t0014g0094 a0001c0002t0002g0003 a0001c0002t0002g0004 others(5): Show |
8 | HG02109.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1479+529_1479+530d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484541 | ||||||
chr9:68484541 | A | AACACACA others(1): Show |
3 | a0001c0001t0019g0002 a0001c0005t0009g0208 a0001c0005t0009g0210 |
3 | HG01255.hp2 HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1479+523_1479+530d others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484541 | ||||||
chr9:68484541 | A | AACACACA others(3): Show |
4 | a0001c0001t0006g0008 a0001c0001t0007g0169 a0001c0001t0019g0001 others(1): Show |
4 | HG01175.hp1 HG02258.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1479+521_1479+530d others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484541 | ||||||
chr9:68484541 | A | AACACACA others(5): Show |
3 | a0001c0001t0007g0233 a0001c0001t0015g0116 a0004c0018t0006g0237 |
3 | HG02055.hp1 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1479+519_1479+530d others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484541 | ||||||
chr9:68484541 | A | AACACACA others(7): Show |
2 | a0001c0001t0007g0165 a0001c0001t0007g0171 |
2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1479+517_1479+530d others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484541 | ||||||
chr9:68484541 | A | ACACACAC others(4): Show |
1 | a0001c0001t0015g0097 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1479+493_1479+494i others(13): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68484541 | |||||||
chr9:68484541 | AAC | A | 171 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(168): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1479+529_1479+530d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484541 | ||||||
chr9:68484541 | AACAC | A | 3 | a0001c0001t0001g0124 a0001c0002t0001g0155 a0001c0003t0005g0012 |
3 | HG02109.hp2 HG03490.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1479+527_1479+530d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484541 | ||||||
chr9:68484541 | AACACAC | A | 6 | a0001c0001t0003g0166 a0001c0001t0012g0187 a0001c0001t0017g0221 others(3): Show |
6 | HG01081.hp2 HG03490.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1479+525_1479+530d others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484541 | ||||||
chr9:68484541 | AACACACA others(7): Show |
A | 1 | a0001c0001t0007g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1479+517_1479+530d others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484541 | ||||||
chr9:68484577 | CA | C | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1479+533delA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484577 | ||||||
chr9:68484580 | A | C | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1479+532A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68484580 | |||||||
chr9:68484598 | C | CA | 39 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0142 others(36): Show |
39 | HG00423.hp2 HG00642.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1479+561dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68484598 | ||||||
chr9:68484639 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1479+591A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68484639 | |||||||
chr9:68484671 | T | C | 1 | a0001c0001t0015g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1479+623T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68484671 | |||||||
chr9:68484713 | G | A | 24 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0005g0141 others(21): Show |
24 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1479+665G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68484713 | |||||||
chr9:68484804 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1479+756A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68484804 | |||||||
chr9:68485011 | C | T | 1 | a0001c0002t0008g0034 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1479+963C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485011 | |||||||
chr9:68485012 | G | A | 2 | a0001c0001t0005g0141 a0001c0002t0008g0044 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1479+964G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485012 | |||||||
chr9:68485058 | C | T | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1479+1010C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485058 | |||||||
chr9:68485224 | C | A | 25 | a0001c0001t0001g0086 a0001c0001t0001g0148 a0001c0001t0002g0005 others(22): Show |
25 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1479+1176C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485224 | |||||||
chr9:68485230 | T | G | 200 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(197): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1479+1182T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485230 | |||||||
chr9:68485379 | G | A | 1 | a0001c0004t0024g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1479+1331G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485379 | |||||||
chr9:68485432 | C | T | 1 | a0001c0002t0002g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1479+1384C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485432 | |||||||
chr9:68485591 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1479+1543C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485591 | |||||||
chr9:68485592 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1479+1544G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485592 | |||||||
chr9:68485667 | A | G | 5 | a0001c0001t0004g0151 a0001c0001t0007g0168 a0001c0001t0015g0105 others(2): Show |
5 | HG02257.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1479+1619A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485667 | |||||||
chr9:68485792 | C | T | 7 | a0001c0001t0006g0008 a0001c0001t0007g0165 a0001c0001t0007g0169 others(4): Show |
7 | HG01175.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1479+1744C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485792 | |||||||
chr9:68485952 | G | A | 1 | a0001c0003t0005g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1479+1904G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68485952 | |||||||
chr9:68486121 | A | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1479+2073A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486121 | |||||||
chr9:68486232 | T | C | 18 | a0001c0001t0004g0085 a0001c0001t0006g0008 a0001c0001t0007g0165 others(15): Show |
18 | HG01175.hp1 HG01255.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1479+2184T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486232 | |||||||
chr9:68486433 | C | T | 31 | a0001c0001t0001g0086 a0001c0001t0001g0148 a0001c0001t0002g0005 others(28): Show |
31 | HG00323.hp2 HG00423.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1479+2385C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486433 | |||||||
chr9:68486494 | G | T | 1 | a0001c0001t0011g0212 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1479+2446G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486494 | |||||||
chr9:68486502 | G | A | 1 | a0001c0001t0007g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1479+2454G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486502 | |||||||
chr9:68486571 | A | G | 12 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0082 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1479+2523A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486571 | |||||||
chr9:68486597 | A | G | 5 | a0001c0001t0007g0165 a0001c0001t0007g0169 a0001c0001t0007g0171 others(2): Show |
5 | HG02630.hp1 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1479+2549A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486597 | |||||||
chr9:68486696 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1479+2648G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486696 | |||||||
chr9:68486763 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0200 |
2 | HG01496.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1479+2715G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486763 | |||||||
chr9:68486795 | C | T | 4 | a0001c0001t0004g0151 a0001c0001t0015g0105 a0001c0006t0004g0122 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1479+2747C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486795 | |||||||
chr9:68486884 | C | G | 7 | a0001c0001t0006g0008 a0001c0001t0007g0165 a0001c0001t0007g0169 others(4): Show |
7 | HG01175.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1479+2836C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486884 | |||||||
chr9:68486974 | A | T | 4 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0139 others(1): Show |
4 | HG01243.hp2 HG01496.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1479+2926A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68486974 | |||||||
chr9:68487311 | T | C | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1479+3263T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68487311 | |||||||
chr9:68487330 | C | T | 12 | a0001c0001t0002g0073 a0001c0001t0002g0080 a0001c0001t0004g0178 others(9): Show |
12 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1479+3282C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68487330 | |||||||
chr9:68487429 | T | TTC | 2 | a0001c0001t0001g0095 a0001c0002t0002g0031 |
2 | HG00438.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1479+3399_1479+340 others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487429 | ||||||
chr9:68487429 | T | TTCTC | 20 | a0001c0001t0001g0110 a0001c0001t0001g0176 a0001c0001t0001g0181 others(17): Show |
20 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1479+3397_1479+340 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487429 | ||||||
chr9:68487429 | TTC | T | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1479+3399_1479+340 others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487429 | ||||||
chr9:68487447 | C | CTCTCTCT others(1): Show |
29 | a0001c0001t0002g0073 a0001c0001t0002g0080 a0001c0001t0004g0085 others(26): Show |
29 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1479+3400_1479+340 others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487447 | ||||||
chr9:68487447 | C | CTCTCTG | 11 | a0001c0001t0006g0008 a0001c0001t0007g0165 a0001c0001t0007g0169 others(8): Show |
11 | HG01175.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1479+3400_1479+340 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487447 | ||||||
chr9:68487447 | C | CTCTG | 69 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(66): Show |
69 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1479+3400_1479+340 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487447 | ||||||
chr9:68487447 | C | G | 3 | a0001c0001t0004g0151 a0001c0006t0004g0122 a0001c0014t0004g0018 |
3 | HG02451.hp2 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1479+3399C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68487447 | |||||||
chr9:68487458 | G | A | 3 | a0001c0001t0001g0183 a0001c0001t0021g0207 a0001c0002t0002g0067 |
3 | HG00735.hp2 HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1479+3410G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68487458 | |||||||
chr9:68487463 | T | TAC | 40 | a0001c0001t0001g0086 a0001c0001t0001g0100 a0001c0001t0001g0102 others(37): Show |
40 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(37): Show |
intron_variant | MODIFIER | c.1479+3449_1479+345 others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487463 | ||||||
chr9:68487463 | T | TACAC | 64 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(61): Show |
64 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1479+3447_1479+345 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487463 | ||||||
chr9:68487463 | T | TACACAC | 8 | a0001c0001t0002g0005 a0001c0001t0006g0008 a0001c0001t0006g0077 others(5): Show |
8 | HG02083.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1479+3445_1479+345 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487463 | ||||||
chr9:68487463 | T | TACACACA others(1): Show |
23 | a0001c0001t0002g0073 a0001c0001t0002g0080 a0001c0001t0004g0178 others(20): Show |
23 | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1479+3443_1479+345 others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487463 | ||||||
chr9:68487463 | T | TACACACA others(3): Show |
2 | a0001c0004t0024g0240 a0001c0005t0014g0087 |
2 | HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1479+3441_1479+345 others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487463 | ||||||
chr9:68487463 | T | TACACACA others(5): Show |
3 | a0001c0001t0014g0094 a0003c0008t0026g0234 a0003c0008t0027g0235 |
3 | HG02109.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1479+3439_1479+345 others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487463 | ||||||
chr9:68487463 | TAC | T | 5 | a0001c0001t0001g0124 a0001c0001t0004g0154 a0001c0001t0007g0168 others(2): Show |
5 | HG02109.hp2 HG03225.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1479+3449_1479+345 others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487463 | ||||||
chr9:68487463 | TACAC | T | 12 | a0001c0001t0001g0101 a0001c0001t0001g0174 a0001c0001t0001g0175 others(9): Show |
12 | HG00140.hp2 HG00323.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1479+3447_1479+345 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487463 | ||||||
chr9:68487463 | TACACACA others(1): Show |
T | 3 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 |
3 | HG03195.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1479+3443_1479+345 others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68487463 | ||||||
chr9:68487497 | C | A | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1479+3449C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68487497 | |||||||
chr9:68487593 | T | C | 1 | a0005c0015t0012g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1479+3545T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68487593 | |||||||
chr9:68487813 | T | C | 239 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(236): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1479+3765T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68487813 | |||||||
chr9:68487821 | C | T | 3 | a0001c0001t0014g0094 a0003c0008t0026g0234 a0003c0008t0027g0235 |
3 | HG02109.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1479+3773C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68487821 | |||||||
chr9:68487992 | G | A | 1 | a0001c0006t0004g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1479+3944G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68487992 | |||||||
chr9:68488062 | T | A | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1479+4014T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68488062 | |||||||
chr9:68488062 | T | G | 1 | a0001c0001t0002g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1479+4014T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68488062 | |||||||
chr9:68488187 | G | A | 1 | a0001c0002t0013g0047 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1479+4139G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68488187 | |||||||
chr9:68488490 | G | T | 40 | a0001c0001t0002g0073 a0001c0001t0002g0080 a0001c0001t0004g0085 others(37): Show |
40 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1479+4442G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68488490 | |||||||
chr9:68488559 | C | T | 29 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0004g0151 others(26): Show |
29 | HG00423.hp2 HG00642.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1479+4511C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68488559 | |||||||
chr9:68488942 | T | C | 1 | a0001c0014t0004g0018 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1479+4894T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68488942 | |||||||
chr9:68489020 | C | T | 1 | a0001c0002t0002g0052 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1479+4972C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489020 | |||||||
chr9:68489095 | C | G | 3 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 |
3 | HG03195.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1479+5047C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489095 | |||||||
chr9:68489321 | C | G | 4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1479+5273C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489321 | |||||||
chr9:68489423 | A | ATGT | 4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1479+5398_1479+540 others(7): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68489423 | ||||||
chr9:68489423 | ATGT | A | 70 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0073 others(67): Show |
70 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1479+5398_1479+540 others(7): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68489423 | ||||||
chr9:68489427 | T | C | 4 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0004t0002g0238 others(1): Show |
4 | HG01891.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1479+5379T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489427 | |||||||
chr9:68489432 | T | C | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1479+5384T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489432 | |||||||
chr9:68489469 | C | CT | 99 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(96): Show |
99 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1479+5436dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68489469 | ||||||
chr9:68489613 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1479+5565C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489613 | |||||||
chr9:68489657 | G | C | 1 | a0001c0001t0006g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1479+5609G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489657 | |||||||
chr9:68489663 | T | C | 100 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(97): Show |
100 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1479+5615T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489663 | |||||||
chr9:68489735 | T | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0186 |
2 | HG00140.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1479+5687T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489735 | |||||||
chr9:68489838 | G | A | 5 | a0001c0003t0009g0229 a0001c0003t0009g0230 a0001c0004t0006g0241 others(2): Show |
5 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1479+5790G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489838 | |||||||
chr9:68489912 | TC | T | 42 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(39): Show |
42 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1479+5865delC | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68489912 | |||||||
chr9:68490135 | C | A | 1 | a0001c0001t0002g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1479+6087C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68490135 | |||||||
chr9:68490357 | T | C | 88 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(85): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1479+6309T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68490357 | |||||||
chr9:68490496 | A | G | 4 | a0001c0001t0004g0151 a0001c0001t0007g0168 a0001c0006t0004g0122 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1479+6448A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68490496 | |||||||
chr9:68490503 | C | T | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1479+6455C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68490503 | |||||||
chr9:68490539 | A | G | 12 | a0001c0001t0004g0085 a0001c0001t0007g0232 a0001c0001t0015g0097 others(9): Show |
12 | HG01255.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1479+6491A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68490539 | |||||||
chr9:68490806 | C | G | 51 | a0001c0001t0001g0086 a0001c0001t0002g0005 a0001c0001t0002g0073 others(48): Show |
51 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1479+6758C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68490806 | |||||||
chr9:68490961 | T | G | 5 | a0001c0001t0001g0181 a0001c0001t0003g0170 a0001c0001t0003g0194 others(2): Show |
5 | HG01071.hp2 HG01169.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1479+6913T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68490961 | |||||||
chr9:68490976 | T | A | 2 | a0001c0001t0005g0141 a0001c0002t0008g0044 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1479+6928T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68490976 | |||||||
chr9:68491081 | A | G | 8 | a0001c0001t0004g0085 a0001c0001t0007g0232 a0001c0005t0004g0089 others(5): Show |
8 | HG01255.hp2 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1479+7033A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68491081 | |||||||
chr9:68491268 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1479+7220G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68491268 | |||||||
chr9:68491425 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1479+7377C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68491425 | |||||||
chr9:68491596 | T | C | 96 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(93): Show |
96 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1479+7548T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68491596 | |||||||
chr9:68491724 | G | A | 1 | a0001c0001t0007g0167 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1480-7503G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68491724 | |||||||
chr9:68491822 | C | T | 4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-7405C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68491822 | |||||||
chr9:68491827 | C | A | 1 | a0001c0003t0005g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1480-7400C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68491827 | |||||||
chr9:68491946 | A | G | 4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-7281A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68491946 | |||||||
chr9:68492004 | T | A | 1 | a0001c0002t0002g0031 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1480-7223T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492004 | |||||||
chr9:68492103 | A | G | 99 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0099 others(96): Show |
99 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1480-7124A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492103 | |||||||
chr9:68492228 | G | T | 1 | a0001c0001t0015g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1480-6999G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492228 | |||||||
chr9:68492357 | C | T | 1 | a0001c0002t0002g0055 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1480-6870C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492357 | |||||||
chr9:68492368 | A | G | 3 | a0001c0001t0010g0216 a0001c0001t0010g0217 a0001c0002t0008g0029 |
3 | HG02027.hp1 NA18980.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1480-6859A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492368 | |||||||
chr9:68492667 | G | A | 1 | a0001c0003t0005g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1480-6560G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492667 | |||||||
chr9:68492734 | G | A | 214 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(211): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1480-6493G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492734 | |||||||
chr9:68492759 | G | T | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1480-6468G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492759 | |||||||
chr9:68492797 | GT | G | 4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-6423delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68492797 | ||||||
chr9:68492910 | C | G | 2 | a0001c0002t0002g0041 a0001c0002t0002g0042 |
2 | HG02135.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1480-6317C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492910 | |||||||
chr9:68492916 | C | T | 7 | a0001c0001t0006g0008 a0001c0001t0007g0165 a0001c0001t0007g0169 others(4): Show |
7 | HG01175.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1480-6311C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492916 | |||||||
chr9:68492917 | G | C | 1 | a0001c0004t0006g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1480-6310G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492917 | |||||||
chr9:68492924 | A | G | 1 | a0001c0005t0004g0089 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1480-6303A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68492924 | |||||||
chr9:68493212 | G | C | 4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG00323.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-6015G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68493212 | |||||||
chr9:68493341 | A | G | 21 | a0001c0001t0002g0073 a0001c0001t0002g0080 a0001c0001t0004g0178 others(18): Show |
21 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1480-5886A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68493341 | |||||||
chr9:68493516 | G | A | 12 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0082 others(9): Show |
12 | HG00323.hp1 HG00639.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1480-5711G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68493516 | |||||||
chr9:68493610 | C | G | 5 | a0001c0001t0004g0151 a0001c0001t0007g0168 a0001c0001t0015g0105 others(2): Show |
5 | HG02257.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480-5617C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68493610 | |||||||
chr9:68493614 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1480-5613C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68493614 | |||||||
chr9:68493768 | C | T | 1 | a0001c0002t0002g0068 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1480-5459C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68493768 | |||||||
chr9:68493807 | G | A | 2 | a0001c0005t0014g0087 a0001c0005t0014g0088 |
2 | HG06807.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1480-5420G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68493807 | |||||||
chr9:68494209 | A | T | 110 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0099 others(107): Show |
110 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1480-5018A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68494209 | |||||||
chr9:68494230 | A | T | 3 | a0001c0001t0014g0094 a0003c0008t0026g0234 a0003c0008t0027g0235 |
3 | HG02109.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1480-4997A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68494230 | |||||||
chr9:68494376 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1480-4851T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68494376 | |||||||
chr9:68494555 | A | G | 3 | a0001c0002t0002g0036 a0001c0002t0002g0037 a0001c0002t0002g0066 |
3 | HG02056.hp2 NA18975.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1480-4672A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68494555 | |||||||
chr9:68494620 | T | C | 16 | a0001c0001t0004g0085 a0001c0001t0004g0151 a0001c0001t0007g0168 others(13): Show |
16 | HG01255.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1480-4607T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68494620 | |||||||
chr9:68494812 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0131 |
2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1480-4415A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68494812 | |||||||
chr9:68494815 | T | C | 3 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 |
3 | HG03195.hp2 HG03471.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1480-4412T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68494815 | |||||||
chr9:68494845 | T | C | 1 | a0001c0004t0024g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1480-4382T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68494845 | |||||||
chr9:68495074 | A | C | 5 | a0001c0001t0004g0151 a0001c0001t0007g0168 a0001c0001t0009g0119 others(2): Show |
5 | HG02257.hp2 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480-4153A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68495074 | |||||||
chr9:68495219 | C | T | 7 | a0001c0001t0004g0085 a0001c0001t0007g0232 a0001c0005t0004g0089 others(4): Show |
7 | HG01255.hp2 HG02647.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1480-4008C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68495219 | |||||||
chr9:68495300 | G | C | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1480-3927G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68495300 | |||||||
chr9:68495671 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1480-3556T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68495671 | |||||||
chr9:68495957 | T | C | 1 | a0001c0005t0004g0089 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1480-3270T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68495957 | |||||||
chr9:68495975 | C | G | 4 | a0001c0001t0004g0151 a0001c0001t0007g0168 a0001c0001t0015g0105 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-3252C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68495975 | |||||||
chr9:68496094 | A | AAC | 8 | a0001c0001t0006g0008 a0001c0001t0007g0165 a0001c0001t0007g0169 others(5): Show |
8 | HG01175.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1480-3133_1480-313 others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68496094 | |||||||
chr9:68496132 | G | A | 1 | a0001c0001t0005g0137 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1480-3095G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68496132 | |||||||
chr9:68496134 | T | C | 4 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(1): Show |
4 | HG02572.hp1 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480-3093T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68496134 | |||||||
chr9:68496781 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1480-2446G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68496781 | |||||||
chr9:68496846 | G | A | 2 | a0001c0001t0003g0120 a0001c0001t0003g0172 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1480-2381G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68496846 | |||||||
chr9:68496979 | CACGTGTA others(3): Show |
C | 7 | a0001c0002t0002g0021 a0001c0002t0002g0023 a0001c0002t0002g0024 others(4): Show |
7 | HG00099.hp2 HG00280.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1480-2245_1480-223 others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 68496979 | ||||||
chr9:68496994 | C | T | 94 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0143 others(91): Show |
94 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1480-2233C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68496994 | |||||||
chr9:68497241 | A | G | 2 | a0001c0001t0004g0151 a0001c0014t0004g0018 |
2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1480-1986A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68497241 | |||||||
chr9:68497255 | C | T | 19 | a0001c0001t0001g0086 a0001c0001t0005g0141 a0001c0001t0010g0216 others(16): Show |
19 | HG00597.hp2 HG02027.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.1480-1972C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68497255 | |||||||
chr9:68497258 | C | T | 223 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(220): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1480-1969C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68497258 | |||||||
chr9:68497429 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1480-1798A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68497429 | |||||||
chr9:68497458 | A | G | 1 | a0001c0001t0007g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1480-1769A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68497458 | |||||||
chr9:68497878 | G | T | 1 | a0001c0006t0004g0122 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1480-1349G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68497878 | |||||||
chr9:68498015 | G | A | 3 | a0001c0001t0002g0080 a0001c0001t0003g0204 a0001c0001t0003g0205 |
3 | HG00099.hp1 HG01168.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1480-1212G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68498015 | |||||||
chr9:68498021 | C | G | 1 | a0001c0004t0002g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1480-1206C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68498021 | |||||||
chr9:68498369 | A | G | 1 | a0001c0002t0013g0048 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1480-858A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68498369 | |||||||
chr9:68498474 | G | A | 195 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(192): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1480-753G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68498474 | |||||||
chr9:68498534 | C | T | 43 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(40): Show |
43 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.1480-693C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68498534 | |||||||
chr9:68498568 | A | G | 100 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(97): Show |
100 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1480-659A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68498568 | |||||||
chr9:68498919 | C | T | 223 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(220): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1480-308C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68498919 | |||||||
chr9:68498991 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1480-236C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68498991 | |||||||
chr9:68499218 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1480-9T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 9/10 | chr9 | 68499218 | |||||||
chr9:68499396 | C | T | 65 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0143 others(62): Show |
65 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1614+35C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68499396 | |||||||
chr9:68499516 | A | G | 1 | a0001c0002t0002g0010 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1614+155A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68499516 | |||||||
chr9:68499701 | T | C | 194 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(191): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1614+340T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68499701 | |||||||
chr9:68499707 | C | T | 194 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(191): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1614+346C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68499707 | |||||||
chr9:68499773 | C | T | 1 | a0001c0011t0002g0033 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1614+412C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68499773 | |||||||
chr9:68499893 | C | A | 86 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0143 others(83): Show |
86 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1614+532C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68499893 | |||||||
chr9:68500113 | A | AT | 103 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0143 others(100): Show |
103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1614+758dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68500113 | ||||||
chr9:68500601 | G | A | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1614+1240G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68500601 | |||||||
chr9:68500868 | G | A | 1 | a0001c0005t0009g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1614+1507G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68500868 | |||||||
chr9:68500912 | C | T | 2 | a0001c0001t0005g0141 a0001c0002t0008g0044 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1614+1551C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68500912 | |||||||
chr9:68500938 | G | A | 1 | a0001c0002t0023g0061 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1614+1577G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68500938 | |||||||
chr9:68501075 | T | C | 78 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0143 others(75): Show |
78 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1614+1714T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68501075 | |||||||
chr9:68501285 | C | T | 6 | a0001c0001t0014g0094 a0001c0004t0024g0240 a0001c0005t0014g0087 others(3): Show |
6 | HG02109.hp1 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1614+1924C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68501285 | |||||||
chr9:68501395 | A | C | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1614+2034A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68501395 | |||||||
chr9:68501709 | T | A | 9 | a0001c0001t0014g0094 a0001c0004t0024g0240 a0001c0005t0004g0089 others(6): Show |
9 | HG01255.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1614+2348T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68501709 | |||||||
chr9:68501880 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1614+2519C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68501880 | |||||||
chr9:68501927 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1614+2566T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68501927 | |||||||
chr9:68502039 | C | T | 86 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0143 others(83): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1614+2678C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68502039 | |||||||
chr9:68502141 | T | A | 2 | a0001c0003t0009g0229 a0001c0003t0009g0230 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1614+2780T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68502141 | |||||||
chr9:68502328 | C | CAAAAGGG others(99): Show |
1 | a0004c0013t0001g0146 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1614+3001_1614+300 others(110): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68502328 | ||||||
chr9:68502363 | T | C | 86 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0143 others(83): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1614+3002T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68502363 | |||||||
chr9:68502398 | T | C | 2 | a0001c0001t0003g0120 a0001c0001t0003g0172 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1614+3037T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68502398 | |||||||
chr9:68502554 | G | A | 5 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0007g0188 others(2): Show |
5 | HG02809.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1614+3193G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68502554 | |||||||
chr9:68502607 | C | T | 86 | a0001c0001t0001g0095 a0001c0001t0001g0110 a0001c0001t0001g0143 others(83): Show |
86 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1614+3246C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68502607 | |||||||
chr9:68502658 | A | G | 1 | a0002c0009t0016g0246 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1614+3297A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68502658 | |||||||
chr9:68502677 | A | ATTTG | 12 | a0001c0001t0014g0094 a0001c0002t0002g0027 a0001c0002t0002g0041 others(9): Show |
12 | HG01255.hp2 HG02109.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.1614+3340_1614+334 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68502677 | ||||||
chr9:68502677 | ATTTG | A | 9 | a0001c0001t0002g0072 a0001c0001t0004g0178 a0001c0001t0006g0075 others(6): Show |
9 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1614+3340_1614+334 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68502677 | ||||||
chr9:68502736 | T | A | 6 | a0001c0001t0001g0164 a0001c0002t0002g0035 a0001c0003t0001g0006 others(3): Show |
6 | NA18944.hp2 NA18963.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614+3375T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68502736 | |||||||
chr9:68502808 | G | A | 199 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1614+3447G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68502808 | |||||||
chr9:68502891 | G | A | 2 | a0001c0004t0002g0238 a0001c0004t0002g0242 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1614+3530G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68502891 | |||||||
chr9:68503053 | T | G | 1 | a0001c0019t0006g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1614+3692T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68503053 | |||||||
chr9:68503057 | T | A | 1 | a0001c0005t0009g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1614+3696T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68503057 | |||||||
chr9:68503175 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1614+3814A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68503175 | |||||||
chr9:68503226 | G | C | 1 | a0001c0004t0025g0236 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1614+3865G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68503226 | |||||||
chr9:68503417 | A | G | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1614+4056A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68503417 | |||||||
chr9:68503614 | C | G | 24 | a0001c0001t0004g0085 a0001c0001t0004g0103 a0001c0001t0004g0104 others(21): Show |
24 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1614+4253C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68503614 | |||||||
chr9:68503968 | G | C | 21 | a0001c0001t0001g0142 a0001c0001t0001g0160 a0001c0001t0001g0162 others(18): Show |
21 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1614+4607G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68503968 | |||||||
chr9:68504110 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1614+4749C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68504110 | |||||||
chr9:68504284 | T | C | 199 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1614+4923T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68504284 | |||||||
chr9:68504445 | G | C | 44 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0101 others(41): Show |
44 | HG00140.hp1 HG00423.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1614+5084G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68504445 | |||||||
chr9:68504602 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0021g0207 a0001c0002t0002g0067 |
3 | HG00735.hp2 HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1614+5241C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68504602 | |||||||
chr9:68504621 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1614+5260G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68504621 | |||||||
chr9:68504822 | T | C | 10 | a0001c0001t0009g0119 a0001c0001t0014g0094 a0001c0004t0024g0240 others(7): Show |
10 | HG01255.hp2 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1614+5461T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68504822 | |||||||
chr9:68505097 | T | C | 199 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1614+5736T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68505097 | |||||||
chr9:68505142 | A | T | 1 | a0001c0001t0005g0137 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1614+5781A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68505142 | |||||||
chr9:68505480 | T | A | 5 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0007g0188 others(2): Show |
5 | HG02809.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1614+6119T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68505480 | |||||||
chr9:68505590 | G | C | 1 | a0001c0004t0002g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1614+6229G>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68505590 | |||||||
chr9:68505678 | C | A | 5 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0007g0188 others(2): Show |
5 | HG02809.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1614+6317C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68505678 | |||||||
chr9:68505818 | A | G | 24 | a0001c0001t0004g0085 a0001c0001t0004g0103 a0001c0001t0004g0104 others(21): Show |
24 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1614+6457A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68505818 | |||||||
chr9:68505847 | A | G | 1 | a0001c0001t0018g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1614+6486A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68505847 | |||||||
chr9:68506187 | G | A | 5 | a0001c0001t0007g0165 a0001c0001t0007g0169 a0001c0001t0007g0171 others(2): Show |
5 | HG02630.hp1 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1614+6826G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68506187 | |||||||
chr9:68506290 | A | G | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1614+6929A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68506290 | |||||||
chr9:68506594 | T | C | 8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0002g0074 others(5): Show |
8 | HG00438.hp2 NA18940.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+7233T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68506594 | |||||||
chr9:68507052 | G | A | 1 | a0001c0002t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1614+7691G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68507052 | |||||||
chr9:68507506 | C | T | 1 | a0001c0002t0002g0035 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1614+8145C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68507506 | |||||||
chr9:68507561 | C | T | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1614+8200C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68507561 | |||||||
chr9:68507587 | AT | A | 195 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(192): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1614+8242delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68507587 | ||||||
chr9:68507677 | C | T | 5 | a0001c0001t0014g0094 a0001c0004t0024g0240 a0001c0005t0014g0087 others(2): Show |
5 | HG02109.hp1 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1614+8316C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68507677 | |||||||
chr9:68507751 | T | C | 127 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0101 others(124): Show |
127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1614+8390T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68507751 | |||||||
chr9:68507762 | T | G | 6 | a0001c0001t0001g0139 a0001c0001t0004g0113 a0001c0001t0004g0138 others(3): Show |
6 | HG01496.hp1 HG02809.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614+8401T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68507762 | |||||||
chr9:68507791 | G | A | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1614+8430G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68507791 | |||||||
chr9:68507935 | G | A | 5 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0007g0188 others(2): Show |
5 | HG02809.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1614+8574G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68507935 | |||||||
chr9:68507978 | A | G | 57 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(54): Show |
57 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1614+8617A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68507978 | |||||||
chr9:68507996 | G | A | 1 | a0001c0001t0010g0214 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1614+8635G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68507996 | |||||||
chr9:68508067 | T | C | 199 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1614+8706T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68508067 | |||||||
chr9:68508586 | A | G | 2 | a0001c0001t0019g0001 a0001c0001t0019g0002 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1614+9225A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68508586 | |||||||
chr9:68508665 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1614+9304G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68508665 | |||||||
chr9:68508670 | G | A | 1 | a0001c0002t0002g0058 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1614+9309G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68508670 | |||||||
chr9:68508831 | A | G | 57 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(54): Show |
57 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1614+9470A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68508831 | |||||||
chr9:68509000 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1614+9639T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68509000 | |||||||
chr9:68509456 | T | C | 119 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0101 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1614+10095T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68509456 | |||||||
chr9:68509536 | C | T | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1614+10175C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68509536 | |||||||
chr9:68509549 | G | A | 1 | a0001c0001t0015g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1614+10188G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68509549 | |||||||
chr9:68509586 | C | A | 199 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1614+10225C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68509586 | |||||||
chr9:68509597 | C | T | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+10236C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68509597 | |||||||
chr9:68509617 | C | T | 5 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0007g0188 others(2): Show |
5 | HG02809.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1614+10256C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68509617 | |||||||
chr9:68509702 | AG | A | 114 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0101 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1614+10342delG | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68509702 | |||||||
chr9:68509761 | C | T | 199 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(196): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1614+10400C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68509761 | |||||||
chr9:68509930 | C | A | 1 | a0001c0002t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1614+10569C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68509930 | |||||||
chr9:68510146 | A | AT | 5 | a0001c0001t0001g0139 a0001c0001t0003g0170 a0001c0001t0012g0231 others(2): Show |
5 | HG01496.hp1 HG02055.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+10808dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68510146 | ||||||
chr9:68510146 | AT | A | 119 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1614+10808delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68510146 | ||||||
chr9:68510146 | ATT | A | 74 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0110 others(71): Show |
74 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1614+10807_1614+10 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68510146 | ||||||
chr9:68510146 | ATTT | A | 14 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0004g0178 others(11): Show |
14 | HG00280.hp2 HG00738.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.1614+10806_1614+10 others(9): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68510146 | ||||||
chr9:68510146 | ATTTT | A | 7 | a0001c0001t0007g0167 a0001c0001t0009g0211 a0001c0001t0015g0097 others(4): Show |
7 | HG00597.hp1 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1614+10805_1614+10 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68510146 | ||||||
chr9:68510210 | G | A | 1 | a0001c0001t0004g0151 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1614+10849G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68510210 | |||||||
chr9:68510431 | T | G | 1 | a0001c0002t0002g0051 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1614+11070T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68510431 | |||||||
chr9:68510518 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0102 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1614+11157A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68510518 | |||||||
chr9:68510532 | T | A | 1 | a0001c0002t0002g0063 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1614+11171T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68510532 | |||||||
chr9:68510550 | T | G | 1 | a0001c0001t0001g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1614+11189T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68510550 | |||||||
chr9:68510683 | G | T | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1614+11322G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68510683 | |||||||
chr9:68510874 | G | A | 1 | a0001c0004t0002g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1614+11513G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68510874 | |||||||
chr9:68510916 | C | T | 84 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(81): Show |
84 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1614+11555C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68510916 | |||||||
chr9:68511046 | G | A | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+11685G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68511046 | |||||||
chr9:68511214 | C | G | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1614+11853C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68511214 | |||||||
chr9:68511279 | G | T | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+11918G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68511279 | |||||||
chr9:68511346 | G | A | 1 | a0001c0002t0002g0023 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1614+11985G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68511346 | |||||||
chr9:68511350 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1614+11989T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68511350 | |||||||
chr9:68511414 | C | A | 64 | a0001c0001t0001g0095 a0001c0001t0001g0143 a0001c0001t0001g0144 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1614+12053C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68511414 | |||||||
chr9:68511545 | C | CT | 6 | a0001c0001t0003g0194 a0001c0002t0002g0056 a0001c0005t0004g0089 others(3): Show |
6 | HG01106.hp1 HG01255.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614+12209dupT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68511545 | ||||||
chr9:68511545 | C | CTT | 5 | a0001c0001t0020g0157 a0001c0001t0029g0111 a0001c0003t0005g0007 others(2): Show |
5 | HG00642.hp1 HG01081.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1614+12208_1614+12 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68511545 | ||||||
chr9:68511545 | C | CTTT | 33 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0099 others(30): Show |
33 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1614+12207_1614+12 others(9): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68511545 | ||||||
chr9:68511545 | C | CTTTT | 10 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0147 others(7): Show |
10 | HG01243.hp1 HG02135.hp1 HG04199.hp1 others(7): Show |
intron_variant | MODIFIER | c.1614+12206_1614+12 others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68511545 | ||||||
chr9:68511545 | C | CTTTTT | 74 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0102 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.1614+12205_1614+12 others(11): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68511545 | ||||||
chr9:68511545 | C | CTTTTTT | 57 | a0001c0001t0001g0093 a0001c0001t0001g0101 a0001c0001t0001g0108 others(54): Show |
57 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1614+12204_1614+12 others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68511545 | ||||||
chr9:68511545 | CT | C | 6 | a0001c0001t0004g0106 a0001c0001t0015g0097 a0001c0001t0015g0105 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1614+12209delT | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68511545 | ||||||
chr9:68511600 | G | A | 24 | a0001c0001t0004g0085 a0001c0001t0004g0103 a0001c0001t0004g0104 others(21): Show |
24 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1614+12239G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68511600 | |||||||
chr9:68512043 | C | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0102 |
2 | HG01243.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1614+12682C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512043 | |||||||
chr9:68512233 | C | T | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1614+12872C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512233 | |||||||
chr9:68512269 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1614+12908C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512269 | |||||||
chr9:68512360 | C | T | 1 | a0001c0001t0010g0214 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1614+12999C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512360 | |||||||
chr9:68512489 | T | A | 57 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(54): Show |
57 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1614+13128T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512489 | |||||||
chr9:68512559 | C | G | 1 | a0001c0001t0015g0097 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1614+13198C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512559 | |||||||
chr9:68512670 | T | G | 1 | a0001c0001t0015g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1614+13309T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512670 | |||||||
chr9:68512768 | T | C | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1614+13407T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512768 | |||||||
chr9:68512846 | C | T | 3 | a0001c0005t0004g0089 a0001c0005t0009g0208 a0001c0005t0009g0210 |
3 | HG01255.hp2 HG03041.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1614+13485C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512846 | |||||||
chr9:68512867 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0145 |
2 | NA18941.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1614+13506G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512867 | |||||||
chr9:68512967 | C | G | 2 | a0001c0001t0005g0141 a0001c0002t0008g0044 |
2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1614+13606C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68512967 | |||||||
chr9:68513095 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1614+13734A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68513095 | |||||||
chr9:68513218 | T | A | 1 | a0001c0001t0028g0040 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1614+13857T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68513218 | |||||||
chr9:68513228 | C | T | 119 | a0001c0001t0001g0095 a0001c0001t0001g0100 a0001c0001t0001g0101 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1614+13867C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68513228 | |||||||
chr9:68513587 | A | C | 8 | a0001c0001t0004g0178 a0001c0001t0006g0075 a0001c0001t0006g0076 others(5): Show |
8 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1614+14226A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68513587 | |||||||
chr9:68513598 | C | T | 2 | a0001c0001t0005g0159 a0001c0001t0005g0161 |
2 | NA19009.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1614+14237C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68513598 | |||||||
chr9:68513640 | A | G | 1 | a0001c0001t0008g0081 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1614+14279A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68513640 | |||||||
chr9:68513682 | T | C | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1614+14321T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68513682 | |||||||
chr9:68513880 | C | T | 55 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0099 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1614+14519C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68513880 | |||||||
chr9:68513944 | C | T | 9 | a0001c0001t0014g0094 a0001c0004t0024g0240 a0001c0005t0004g0089 others(6): Show |
9 | HG01255.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1614+14583C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68513944 | |||||||
chr9:68513983 | G | A | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+14622G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68513983 | |||||||
chr9:68514093 | G | A | 24 | a0001c0001t0004g0085 a0001c0001t0004g0103 a0001c0001t0004g0104 others(21): Show |
24 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1614+14732G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68514093 | |||||||
chr9:68514215 | G | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0186 |
2 | HG00140.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1614+14854G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68514215 | |||||||
chr9:68514237 | G | T | 2 | a0001c0001t0003g0120 a0001c0001t0003g0172 |
2 | HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1614+14876G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68514237 | |||||||
chr9:68514516 | C | T | 9 | a0001c0001t0014g0094 a0001c0004t0024g0240 a0001c0005t0004g0089 others(6): Show |
9 | HG01255.hp2 HG02109.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-15051C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68514516 | |||||||
chr9:68514673 | T | G | 1 | a0001c0016t0022g0084 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1615-14894T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68514673 | |||||||
chr9:68514725 | G | A | 1 | a0001c0020t0030g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1615-14842G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68514725 | |||||||
chr9:68514784 | C | T | 2 | a0001c0001t0012g0187 a0001c0002t0008g0065 |
2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1615-14783C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68514784 | |||||||
chr9:68514788 | G | A | 6 | a0001c0001t0014g0094 a0001c0004t0024g0240 a0001c0005t0014g0087 others(3): Show |
6 | HG02109.hp1 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-14779G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68514788 | |||||||
chr9:68514810 | G | A | 2 | a0001c0002t0002g0028 a0001c0002t0002g0051 |
2 | HG00423.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1615-14757G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68514810 | |||||||
chr9:68514976 | A | C | 1 | a0001c0001t0003g0195 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1615-14591A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68514976 | |||||||
chr9:68515034 | G | A | 91 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0099 others(88): Show |
91 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1615-14533G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68515034 | |||||||
chr9:68515385 | G | A | 5 | a0001c0001t0004g0085 a0001c0001t0004g0154 a0001c0001t0007g0232 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-14182G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68515385 | |||||||
chr9:68515479 | T | C | 1 | a0001c0002t0002g0023 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1615-14088T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68515479 | |||||||
chr9:68516045 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1615-13522T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68516045 | |||||||
chr9:68516062 | T | G | 145 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0100 others(142): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1615-13505T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68516062 | |||||||
chr9:68516174 | G | T | 13 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0004g0178 others(10): Show |
13 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1615-13393G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68516174 | |||||||
chr9:68516182 | T | C | 13 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0004g0178 others(10): Show |
13 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1615-13385T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68516182 | |||||||
chr9:68516310 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1615-13257G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68516310 | |||||||
chr9:68516495 | G | A | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-13072G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68516495 | |||||||
chr9:68516901 | C | T | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-12666C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68516901 | |||||||
chr9:68517033 | G | A | 10 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0002g0074 others(7): Show |
10 | HG00438.hp2 HG02135.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1615-12534G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68517033 | |||||||
chr9:68517136 | G | A | 1 | a0001c0001t0015g0116 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1615-12431G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68517136 | |||||||
chr9:68517475 | G | A | 3 | a0001c0003t0005g0007 a0001c0003t0005g0012 a0001c0003t0005g0013 |
3 | HG00642.hp1 HG01081.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1615-12092G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68517475 | |||||||
chr9:68517849 | G | A | 5 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0007g0188 others(2): Show |
5 | HG02809.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-11718G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68517849 | |||||||
chr9:68518002 | C | A | 218 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(215): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1615-11565C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68518002 | |||||||
chr9:68518132 | A | G | 1 | a0001c0002t0002g0035 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1615-11435A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68518132 | |||||||
chr9:68518333 | T | C | 1 | a0001c0017t0004g0069 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1615-11234T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68518333 | |||||||
chr9:68518378 | A | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0136 |
2 | HG00609.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1615-11189A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68518378 | |||||||
chr9:68518649 | A | C | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1615-10918A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68518649 | |||||||
chr9:68519083 | CTT | C | 42 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(39): Show |
42 | HG00140.hp1 HG00423.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1615-10483_1615-10 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68519083 | |||||||
chr9:68519093 | T | G | 4 | a0001c0001t0009g0119 a0001c0005t0004g0089 a0001c0005t0009g0208 others(1): Show |
4 | HG01255.hp2 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-10474T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68519093 | |||||||
chr9:68519108 | A | G | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1615-10459A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68519108 | |||||||
chr9:68519141 | A | G | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1615-10426A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68519141 | |||||||
chr9:68519542 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1615-10025G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68519542 | |||||||
chr9:68519661 | T | A | 55 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0099 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1615-9906T>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68519661 | |||||||
chr9:68519897 | C | CAATA | 29 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0127 others(26): Show |
29 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.1615-9631_1615-962 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68519897 | ||||||
chr9:68519897 | C | CAATAAAT others(1): Show |
41 | a0001c0001t0001g0102 a0001c0001t0001g0108 a0001c0001t0001g0114 others(38): Show |
41 | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1615-9635_1615-962 others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68519897 | ||||||
chr9:68519897 | C | CAATAAAT others(5): Show |
4 | a0001c0001t0001g0100 a0001c0001t0001g0179 a0001c0001t0001g0185 others(1): Show |
4 | HG00140.hp1 HG01243.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-9639_1615-962 others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68519897 | ||||||
chr9:68519897 | CAATA | C | 9 | a0001c0001t0004g0154 a0001c0001t0015g0097 a0001c0001t0015g0105 others(6): Show |
9 | HG01255.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1615-9631_1615-962 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68519897 | ||||||
chr9:68519897 | CAATAAAT others(1): Show |
C | 18 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(15): Show |
18 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1615-9635_1615-962 others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68519897 | ||||||
chr9:68520089 | C | CA | 150 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0100 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1615-9464dupA | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68520089 | ||||||
chr9:68520089 | C | CAA | 8 | a0001c0001t0002g0070 a0001c0001t0003g0193 a0001c0001t0015g0097 others(5): Show |
8 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-9465_1615-946 others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68520089 | ||||||
chr9:68520118 | C | T | 6 | a0001c0001t0014g0094 a0001c0004t0024g0240 a0001c0005t0014g0087 others(3): Show |
6 | HG02109.hp1 HG02622.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-9449C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520118 | |||||||
chr9:68520164 | A | T | 1 | a0001c0002t0008g0034 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1615-9403A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520164 | |||||||
chr9:68520176 | C | T | 1 | a0001c0002t0002g0009 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1615-9391C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520176 | |||||||
chr9:68520177 | G | A | 47 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0099 others(44): Show |
47 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1615-9390G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520177 | |||||||
chr9:68520321 | T | G | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1615-9246T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520321 | |||||||
chr9:68520388 | G | A | 233 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1615-9179G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520388 | |||||||
chr9:68520435 | G | A | 1 | a0001c0003t0001g0006 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1615-9132G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520435 | |||||||
chr9:68520539 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1615-9028T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520539 | |||||||
chr9:68520681 | A | G | 1 | a0001c0001t0011g0212 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1615-8886A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520681 | |||||||
chr9:68520889 | T | C | 1 | a0001c0002t0002g0032 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1615-8678T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520889 | |||||||
chr9:68520943 | G | T | 1 | a0001c0001t0011g0219 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1615-8624G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68520943 | |||||||
chr9:68521035 | C | A | 5 | a0001c0001t0007g0165 a0001c0001t0007g0169 a0001c0001t0007g0171 others(2): Show |
5 | HG02630.hp1 HG02723.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-8532C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68521035 | |||||||
chr9:68521172 | A | G | 5 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0007g0188 others(2): Show |
5 | HG02809.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-8395A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68521172 | |||||||
chr9:68521381 | G | A | 4 | a0001c0001t0004g0085 a0001c0001t0007g0232 a0001c0005t0009g0209 others(1): Show |
4 | HG02647.hp1 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615-8186G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68521381 | |||||||
chr9:68521782 | C | T | 19 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(16): Show |
19 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1615-7785C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68521782 | |||||||
chr9:68522316 | C | T | 86 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(83): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1615-7251C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68522316 | |||||||
chr9:68522366 | A | G | 19 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(16): Show |
19 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1615-7201A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68522366 | |||||||
chr9:68522509 | G | A | 235 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0095 others(232): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1615-7058G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68522509 | |||||||
chr9:68522676 | G | T | 5 | a0001c0001t0014g0094 a0001c0004t0024g0240 a0001c0005t0014g0087 others(2): Show |
5 | HG02109.hp1 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-6891G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68522676 | |||||||
chr9:68522686 | C | T | 5 | a0001c0001t0004g0085 a0001c0001t0004g0154 a0001c0001t0007g0232 others(2): Show |
5 | HG02647.hp1 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-6881C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68522686 | |||||||
chr9:68522917 | T | C | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1615-6650T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68522917 | |||||||
chr9:68523085 | G | T | 1 | a0001c0001t0020g0156 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1615-6482G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68523085 | |||||||
chr9:68523140 | T | C | 8 | a0001c0001t0004g0178 a0001c0001t0006g0075 a0001c0001t0006g0076 others(5): Show |
8 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-6427T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68523140 | |||||||
chr9:68523669 | T | C | 6 | a0001c0001t0010g0220 a0001c0001t0010g0224 a0001c0001t0012g0118 others(3): Show |
6 | HG02698.hp2 HG03490.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1615-5898T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68523669 | |||||||
chr9:68523721 | G | A | 1 | a0001c0004t0024g0240 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1615-5846G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68523721 | |||||||
chr9:68523791 | A | T | 1 | a0001c0001t0001g0086 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1615-5776A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68523791 | |||||||
chr9:68523886 | G | A | 42 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0099 others(39): Show |
42 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1615-5681G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68523886 | |||||||
chr9:68524314 | C | G | 1 | a0001c0002t0002g0066 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1615-5253C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68524314 | |||||||
chr9:68524394 | G | A | 1 | a0001c0001t0004g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1615-5173G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68524394 | |||||||
chr9:68524462 | T | C | 71 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0096 others(68): Show |
71 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1615-5105T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68524462 | |||||||
chr9:68524790 | C | T | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-4777C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68524790 | |||||||
chr9:68524880 | G | A | 1 | a0001c0001t0020g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1615-4687G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68524880 | |||||||
chr9:68525112 | TGA | T | 10 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0007g0188 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1615-4450_1615-444 others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68525112 | ||||||
chr9:68525177 | AC | A | 19 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(16): Show |
19 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1615-4387delC | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68525177 | ||||||
chr9:68525324 | T | C | 19 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(16): Show |
19 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1615-4243T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68525324 | |||||||
chr9:68525385 | A | G | 5 | a0001c0001t0014g0094 a0001c0004t0024g0240 a0001c0005t0014g0087 others(2): Show |
5 | HG02109.hp1 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-4182A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68525385 | |||||||
chr9:68525485 | T | C | 2 | a0001c0001t0006g0008 a0001c0004t0025g0236 |
2 | HG01175.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1615-4082T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68525485 | |||||||
chr9:68526061 | A | T | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-3506A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526061 | |||||||
chr9:68526064 | AAAAG | A | 19 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(16): Show |
19 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1615-3491_1615-348 others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68526064 | ||||||
chr9:68526156 | T | G | 19 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(16): Show |
19 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1615-3411T>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526156 | |||||||
chr9:68526188 | A | G | 1 | a0001c0002t0002g0067 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1615-3379A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526188 | |||||||
chr9:68526192 | A | G | 1 | a0002c0010t0016g0245 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1615-3375A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526192 | |||||||
chr9:68526210 | A | G | 1 | a0001c0001t0009g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1615-3357A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526210 | |||||||
chr9:68526271 | C | T | 51 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(48): Show |
51 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1615-3296C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526271 | |||||||
chr9:68526323 | C | T | 2 | a0001c0001t0008g0078 a0001c0001t0008g0081 |
2 | HG00609.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1615-3244C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526323 | |||||||
chr9:68526558 | C | T | 2 | a0001c0002t0002g0023 a0001c0002t0002g0024 |
2 | HG01258.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1615-3009C>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526558 | |||||||
chr9:68526574 | T | C | 13 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0004g0178 others(10): Show |
13 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1615-2993T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526574 | |||||||
chr9:68526815 | A | C | 1 | a0001c0001t0001g0174 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1615-2752A>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526815 | |||||||
chr9:68526986 | G | T | 30 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(27): Show |
30 | HG01175.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1615-2581G>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68526986 | |||||||
chr9:68527678 | AG | A | 14 | a0001c0001t0001g0121 a0001c0001t0001g0176 a0001c0001t0002g0080 others(11): Show |
14 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1615-1887delG | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68527678 | ||||||
chr9:68527688 | C | G | 1 | a0001c0001t0010g0214 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1615-1879C>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68527688 | |||||||
chr9:68527693 | T | C | 2 | a0001c0001t0007g0168 a0001c0019t0006g0239 |
2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1615-1874T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68527693 | |||||||
chr9:68527734 | G | GCTTGT | 72 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(69): Show |
72 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1615-1833_1615-183 others(9): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68527734 | |||||||
chr9:68527735 | T | C | 72 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0099 others(69): Show |
72 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1615-1832T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68527735 | |||||||
chr9:68527789 | T | C | 19 | a0001c0001t0004g0103 a0001c0001t0004g0104 a0001c0001t0004g0106 others(16): Show |
19 | HG01175.hp1 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1615-1778T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68527789 | |||||||
chr9:68528015 | T | C | 1 | a0001c0002t0002g0026 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1615-1552T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68528015 | |||||||
chr9:68528520 | A | T | 48 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0001t0001g0112 others(45): Show |
48 | HG00323.hp2 HG00408.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1615-1047A>T | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68528520 | |||||||
chr9:68528534 | G | A | 1 | a0001c0001t0004g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1615-1033G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68528534 | |||||||
chr9:68528594 | A | G | 1 | a0001c0002t0002g0060 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1615-973A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68528594 | |||||||
chr9:68528700 | T | C | 5 | a0001c0001t0014g0094 a0001c0004t0024g0240 a0001c0005t0014g0087 others(2): Show |
5 | HG02109.hp1 HG02970.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-867T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68528700 | |||||||
chr9:68528738 | T | C | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-829T>C | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68528738 | |||||||
chr9:68528984 | A | G | 152 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1615-583A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68528984 | |||||||
chr9:68528986 | G | A | 1 | a0001c0001t0007g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1615-581G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68528986 | |||||||
chr9:68528987 | C | A | 1 | a0001c0001t0007g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1615-580C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68528987 | |||||||
chr9:68529049 | C | A | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-518C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68529049 | |||||||
chr9:68529139 | A | G | 1 | a0001c0004t0002g0243 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1615-428A>G | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68529139 | |||||||
chr9:68529164 | C | CGT | 37 | a0001c0001t0001g0095 a0001c0001t0001g0121 a0001c0001t0001g0145 others(34): Show |
37 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.1615-357_1615-356d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | C | CGTGT | 37 | a0001c0001t0001g0086 a0001c0001t0001g0099 a0001c0001t0001g0112 others(34): Show |
37 | HG00423.hp2 HG00438.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1615-359_1615-356d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | C | CGTGTGT | 28 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0110 others(25): Show |
28 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.1615-361_1615-356d others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | C | CGTGTGTG others(1): Show |
14 | a0001c0001t0001g0176 a0001c0001t0001g0199 a0001c0001t0004g0178 others(11): Show |
14 | HG00280.hp2 HG00673.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1615-363_1615-356d others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0021g0134 a0001c0002t0002g0042 |
2 | HG01433.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1615-365_1615-356d others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | C | CGTGTGTG others(5): Show |
4 | a0001c0001t0007g0167 a0001c0001t0018g0226 a0001c0001t0021g0207 others(1): Show |
4 | HG00597.hp1 HG00735.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1615-367_1615-356d others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | CGT | C | 24 | a0001c0001t0001g0115 a0001c0001t0001g0160 a0001c0001t0001g0175 others(21): Show |
24 | HG00099.hp1 HG00735.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1615-357_1615-356d others(4): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | CGTGT | C | 35 | a0001c0001t0001g0101 a0001c0001t0001g0108 a0001c0001t0001g0142 others(32): Show |
35 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1615-359_1615-356d others(6): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | CGTGTGT | C | 6 | a0001c0001t0001g0124 a0001c0001t0001g0177 a0001c0001t0002g0005 others(3): Show |
6 | HG02523.hp2 HG02572.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-361_1615-356d others(8): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0014g0094 a0001c0002t0002g0060 a0001c0002t0002g0063 others(3): Show |
6 | HG00323.hp2 HG01109.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-363_1615-356d others(10): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | CGTGTGTG others(3): Show |
C | 5 | a0001c0001t0015g0097 a0001c0001t0015g0105 a0001c0001t0015g0116 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-365_1615-356d others(12): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0008g0078 a0001c0001t0008g0081 |
2 | HG00609.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1615-367_1615-356d others(14): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529164 | CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0011g0212 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1615-369_1615-356d others(16): Show |
PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 68529164 | ||||||
chr9:68529290 | C | A | 5 | a0001c0001t0004g0113 a0001c0001t0004g0138 a0001c0001t0009g0119 others(2): Show |
5 | HG02572.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1615-277C>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68529290 | |||||||
chr9:68529512 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1615-55G>A | PGM5 | ENSG00000154330.13 | transcript | ENST00000396396.6 | protein_coding | 10/10 | chr9 | 68529512 |