Item | Value |
---|---|
geneid | 9945 |
ensemblid | ENSG00000131459.13 |
hgncid | 4242 |
symbol | GFPT2 |
name | glutamine-fructose-6-phosphate transaminase 2 |
refseq_nuc | NM_005110.4 |
refseq_prot | NP_005101.1 |
ensembl_nuc | ENST00000253778.13 |
ensembl_prot | ENSP00000253778.8 |
mane_status | MANE Select |
chr | chr5 |
start | 180300698 |
end | 180353336 |
strand | - |
ver | v1.2 |
region | chr5:180300698-180353336 |
region5000 | chr5:180295698-180358336 |
regionname0 | GFPT2_chr5_180300698_180353336 |
regionname5000 | GFPT2_chr5_180295698_180358336 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 682 | 288 | 87 | 52 | 104 | 13 | 30 | 77 | GFPT2_chr5_180295698_180358336 | GFPT2 | MCGIF others(677): Show |
chr5 | 180295698 | 180358336 |
a0002 | 0/0 | 682 | 101 | 7 | 11 | 67 | 4 | 12 | 48 | GFPT2_chr5_180295698_180358336 | GFPT2 | MCGIF others(677): Show |
chr5 | 180295698 | 180358336 |
a0003 | 0/0 | 682 | 18 | 0 | 1 | 14 | 1 | 2 | 14 | GFPT2_chr5_180295698_180358336 | GFPT2 | MCGIF others(677): Show |
chr5 | 180295698 | 180358336 |
a0004 | 0/0 | 682 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | MCGIF others(677): Show |
chr5 | 180295698 | 180358336 |
a0005 | 0/0 | 682 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | MCGIF others(677): Show |
chr5 | 180295698 | 180358336 |
a0006 | 0/0 | 337 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | MCGIF others(332): Show |
chr5 | 180295698 | 180358336 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2046 | 90 | 28 | 24 | 12 | 9 | 15 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0001c0003 | 0/0 | 2046 | 72 | 9 | 13 | 41 | 3 | 6 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0001c0004 | 0/0 | 2046 | 60 | 14 | 10 | 27 | 1 | 8 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0001c0005 | 0/0 | 2046 | 57 | 29 | 5 | 22 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0001c0009 | 0/0 | 2046 | 3 | 3 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0001c0012 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0001c0017 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0001c0018 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0001c0019 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0001c0021 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0002c0002 | 0/0 | 2046 | 89 | 4 | 11 | 61 | 3 | 10 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0002c0007 | 0/0 | 2046 | 6 | 1 | 0 | 4 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0002c0008 | 0/0 | 2046 | 3 | 0 | 0 | 1 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0002c0015 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0002c0020 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0003c0006 | 0/0 | 2046 | 14 | 0 | 1 | 10 | 1 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0003c0013 | 0/0 | 2046 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0003c0014 | 0/0 | 2046 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0004c0011 | 0/0 | 2046 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0005c0010 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2041): Show |
chr5 | 180295698 | 180358336 | ||
a0006c0016 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | ATGTG others(2031): Show |
chr5 | 180295698 | 180358336 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3034 | 76 | 22 | 24 | 11 | 8 | 10 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0001t0005 | 0/0 | 3034 | 11 | 4 | 0 | 1 | 1 | 5 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0001t0009 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0001t0018 | 0/1 | 3025 | 1 | 0 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3020): Show |
chr5 | 180295698 | 180358336 |
a0001c0003t0001 | 0/0 | 3034 | 69 | 7 | 12 | 41 | 3 | 6 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0003t0004 | 0/0 | 3034 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0003t0005 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0003t0014 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0004t0001 | 0/0 | 3034 | 53 | 11 | 10 | 23 | 1 | 8 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0004t0003 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0004t0005 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0004t0008 | 0/0 | 3046 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3041): Show |
chr5 | 180295698 | 180358336 |
a0001c0004t0016 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0004t0020 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3008): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0001 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0002 | 0/0 | 3034 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0003 | 0/0 | 3034 | 24 | 16 | 1 | 7 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0004 | 0/0 | 3034 | 18 | 0 | 2 | 15 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0005 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0007 | 0/0 | 3034 | 3 | 3 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0010 | 0/0 | 3013 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3008): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0011 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0015 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0019 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3008): Show |
chr5 | 180295698 | 180358336 |
a0001c0005t0021 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0009t0001 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0009t0005 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0012t0001 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0017t0001 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0018t0006 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0019t0001 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0001c0021t0001 | 0/0 | 3034 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0002c0002t0001 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0002c0002t0002 | 0/0 | 3034 | 80 | 3 | 7 | 58 | 3 | 9 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0002c0002t0004 | 0/0 | 3034 | 5 | 0 | 4 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0002c0002t0012 | 0/0 | 3016 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3011): Show |
chr5 | 180295698 | 180358336 |
a0002c0002t0013 | 0/0 | 3034 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0002c0002t0017 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0002c0007t0001 | 0/0 | 3034 | 6 | 1 | 0 | 4 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0002c0008t0001 | 0/0 | 3034 | 3 | 0 | 0 | 1 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0002c0015t0001 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0002c0020t0001 | 0/0 | 3034 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0003c0006t0001 | 0/0 | 3034 | 11 | 0 | 1 | 7 | 1 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0003c0006t0006 | 0/0 | 3034 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0003c0013t0001 | 0/0 | 3034 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0003c0014t0001 | 0/0 | 3034 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0004c0011t0002 | 0/0 | 3034 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0005c0010t0001 | 0/0 | 3034 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3029): Show |
chr5 | 180295698 | 180358336 |
a0006c0016t0002 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | AGCTG others(3019): Show |
chr5 | 180295698 | 180358336 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0005g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0001t0018g0358 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0005g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0003t0014g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0005g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0005g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0008g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0016g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0004t0020g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0005g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0007g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0007g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0010g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0010g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0011g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0011g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0015g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0019g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0005t0021g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0009t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0009t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0009t0005g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0012t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0012t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0017t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0018t0006g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0019t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0001c0021t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0004g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0004g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0004g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0012g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0013g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0002t0017g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0007t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0007t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0007t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0007t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0007t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0008t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0008t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0008t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0015t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0002c0020t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0006t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0013t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0013t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0014t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0003c0014t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0004c0011t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0005c0010t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0005c0010t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
a0006c0016t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0006 | t0001 | g0017 | EUR | GBR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0282 | EUR | GBR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0288 | EUR | GBR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0216 | EUR | GBR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0381 | EUR | FIN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0093 | EUR | FIN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00323 | hp1 | a0001 | c0003 | t0001 | g0094 | EUR | FIN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00423 | hp2 | a0001 | c0004 | t0001 | g0188 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00438 | hp2 | a0001 | c0004 | t0001 | g0249 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0316 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0301 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00597 | hp2 | a0001 | c0003 | t0001 | g0247 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00609 | hp1 | a0001 | c0005 | t0004 | g0159 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00621 | hp2 | a0002 | c0020 | t0001 | g0298 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00639 | hp1 | a0001 | c0004 | t0001 | g0042 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00642 | hp1 | a0001 | c0005 | t0004 | g0291 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00642 | hp2 | a0001 | c0004 | t0001 | g0062 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00673 | hp1 | a0001 | c0005 | t0004 | g0163 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0065 | EAS | CHS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00733 | hp2 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0319 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0098 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01074 | hp2 | a0001 | c0004 | t0001 | g0014 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01099 | hp1 | a0002 | c0002 | t0004 | g0025 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01106 | hp1 | a0001 | c0004 | t0001 | g0352 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01109 | hp2 | a0002 | c0002 | t0004 | g0348 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01167 | hp2 | a0001 | c0005 | t0003 | g0234 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0287 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0086 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01192 | hp1 | a0001 | c0003 | t0004 | g0119 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0031 | AMR | PUR | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01255 | hp2 | a0001 | c0004 | t0001 | g0085 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0114 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01261 | hp1 | a0004 | c0011 | t0002 | g0012 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0113 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01346 | hp2 | a0001 | c0004 | t0001 | g0256 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01358 | hp2 | a0001 | c0005 | t0002 | g0082 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01361 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0271 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01496 | hp2 | a0004 | c0011 | t0002 | g0012 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01515 | hp1 | a0002 | c0007 | t0001 | g0351 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0081 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01884 | hp1 | a0001 | c0005 | t0001 | g0341 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01928 | hp2 | a0002 | c0002 | t0004 | g0349 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01934 | hp2 | a0001 | c0004 | t0001 | g0049 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01952 | hp2 | a0001 | c0004 | t0001 | g0197 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01975 | hp1 | a0003 | c0006 | t0001 | g0245 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01978 | hp1 | a0001 | c0004 | t0001 | g0141 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01978 | hp2 | a0001 | c0005 | t0002 | g0107 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01981 | hp1 | a0001 | c0005 | t0004 | g0165 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0279 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01993 | hp1 | a0001 | c0003 | t0001 | g0350 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02004 | hp1 | a0002 | c0002 | t0004 | g0025 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0369 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02040 | hp1 | a0001 | c0005 | t0004 | g0160 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02040 | hp2 | a0001 | c0004 | t0001 | g0068 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02055 | hp2 | a0001 | c0005 | t0011 | g0379 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02056 | hp1 | a0001 | c0003 | t0001 | g0200 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02071 | hp1 | a0001 | c0004 | t0001 | g0055 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02071 | hp2 | a0001 | c0005 | t0003 | g0214 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02074 | hp1 | a0001 | c0004 | t0001 | g0309 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02074 | hp2 | a0001 | c0003 | t0001 | g0057 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02080 | hp1 | a0001 | c0004 | t0001 | g0059 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0289 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02083 | hp1 | a0001 | c0004 | t0001 | g0179 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0354 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0355 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02135 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02145 | hp1 | a0001 | c0005 | t0003 | g0283 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02145 | hp2 | a0001 | c0009 | t0005 | g0375 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02148 | hp1 | a0001 | c0003 | t0001 | g0252 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0108 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02155 | hp1 | a0001 | c0005 | t0003 | g0131 | EAS | CDX | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CDX | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | CDX | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | CDX | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0370 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02257 | hp2 | a0001 | c0005 | t0007 | g0304 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02258 | hp1 | a0001 | c0005 | t0015 | g0250 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02258 | hp2 | a0001 | c0012 | t0001 | g0170 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02280 | hp1 | a0001 | c0005 | t0003 | g0207 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0203 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02451 | hp1 | a0001 | c0004 | t0005 | g0373 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02523 | hp1 | a0001 | c0004 | t0001 | g0053 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | KHV | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0198 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0090 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02615 | hp1 | a0001 | c0005 | t0003 | g0259 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02615 | hp2 | a0001 | c0005 | t0003 | g0212 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0306 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02622 | hp2 | a0001 | c0009 | t0001 | g0180 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02630 | hp1 | a0001 | c0004 | t0001 | g0218 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02647 | hp1 | a0001 | c0004 | t0001 | g0270 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02647 | hp2 | a0001 | c0005 | t0003 | g0213 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02683 | hp2 | a0001 | c0004 | t0001 | g0083 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02717 | hp1 | a0001 | c0005 | t0003 | g0265 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0303 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0269 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02723 | hp2 | a0001 | c0005 | t0003 | g0185 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02735 | hp1 | a0001 | c0003 | t0001 | g0253 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02735 | hp2 | a0002 | c0008 | t0001 | g0228 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0372 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0140 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0335 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0365 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02886 | hp1 | a0001 | c0003 | t0014 | g0336 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02895 | hp1 | a0001 | c0005 | t0003 | g0125 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02895 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02896 | hp1 | a0002 | c0015 | t0001 | g0013 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02897 | hp1 | a0002 | c0015 | t0001 | g0013 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02897 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02922 | hp2 | a0001 | c0005 | t0003 | g0266 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02965 | hp1 | a0005 | c0010 | t0001 | g0133 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02965 | hp2 | a0001 | c0005 | t0019 | g0361 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02970 | hp1 | a0001 | c0005 | t0010 | g0360 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0305 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02976 | hp1 | a0001 | c0004 | t0001 | g0204 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02976 | hp2 | a0001 | c0017 | t0001 | g0232 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03017 | hp1 | a0001 | c0003 | t0001 | g0299 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0137 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03041 | hp1 | a0001 | c0005 | t0003 | g0210 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0367 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03130 | hp1 | a0001 | c0004 | t0001 | g0195 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0110 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03139 | hp1 | a0001 | c0005 | t0003 | g0088 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0169 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03195 | hp2 | a0001 | c0005 | t0001 | g0219 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03209 | hp1 | a0001 | c0005 | t0003 | g0209 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0290 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03225 | hp1 | a0001 | c0005 | t0007 | g0353 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03239 | hp1 | a0003 | c0006 | t0001 | g0017 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03239 | hp2 | a0003 | c0006 | t0001 | g0244 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03453 | hp1 | a0001 | c0005 | t0011 | g0374 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03486 | hp2 | a0001 | c0005 | t0003 | g0033 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0039 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0363 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0364 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0038 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0377 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03516 | hp2 | a0001 | c0005 | t0003 | g0268 | AFR | ESN | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03540 | hp1 | a0001 | c0004 | t0001 | g0344 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03540 | hp2 | a0001 | c0021 | t0001 | g0251 | AFR | GWD | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03579 | hp1 | a0001 | c0004 | t0005 | g0366 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03579 | hp2 | a0005 | c0010 | t0001 | g0132 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03669 | hp1 | a0001 | c0004 | t0001 | g0184 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0380 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0112 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03704 | hp2 | a0001 | c0004 | t0001 | g0056 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0314 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03710 | hp2 | a0002 | c0002 | t0013 | g0027 | SAS | PJL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0376 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03927 | hp1 | a0001 | c0005 | t0004 | g0295 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03927 | hp2 | a0001 | c0004 | t0001 | g0224 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03942 | hp2 | a0001 | c0004 | t0001 | g0227 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG04115 | hp2 | a0001 | c0004 | t0001 | g0187 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0221 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG04184 | hp2 | a0001 | c0004 | t0001 | g0330 | SAS | BEB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG04204 | hp1 | a0002 | c0008 | t0001 | g0226 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0254 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0230 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | CHB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0340 | EAS | CHB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | CHB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18906 | hp1 | a0001 | c0009 | t0001 | g0356 | AFR | YRI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18906 | hp2 | a0002 | c0007 | t0001 | g0211 | AFR | YRI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0310 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18942 | hp2 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18943 | hp1 | a0001 | c0005 | t0004 | g0152 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0276 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18944 | hp2 | a0002 | c0007 | t0001 | g0320 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18946 | hp1 | a0003 | c0006 | t0001 | g0236 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18946 | hp2 | a0003 | c0014 | t0001 | g0302 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18947 | hp2 | a0001 | c0003 | t0001 | g0294 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18949 | hp1 | a0001 | c0004 | t0001 | g0223 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18949 | hp2 | a0001 | c0005 | t0003 | g0172 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18950 | hp1 | a0003 | c0006 | t0001 | g0043 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18950 | hp2 | a0001 | c0005 | t0004 | g0153 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18951 | hp1 | a0001 | c0005 | t0004 | g0058 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0296 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18954 | hp1 | a0002 | c0007 | t0001 | g0022 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18954 | hp2 | a0002 | c0008 | t0001 | g0182 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18957 | hp2 | a0002 | c0002 | t0004 | g0168 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18959 | hp1 | a0003 | c0006 | t0006 | g0067 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18959 | hp2 | a0001 | c0003 | t0001 | g0315 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18960 | hp1 | a0001 | c0004 | t0016 | g0051 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18960 | hp2 | a0001 | c0004 | t0003 | g0183 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18962 | hp1 | a0001 | c0005 | t0004 | g0045 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18964 | hp1 | a0001 | c0004 | t0001 | g0229 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18964 | hp2 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0312 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18966 | hp2 | a0003 | c0013 | t0001 | g0239 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18967 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0347 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18968 | hp2 | a0001 | c0004 | t0001 | g0060 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18969 | hp1 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18969 | hp2 | a0002 | c0007 | t0001 | g0324 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18970 | hp1 | a0003 | c0006 | t0006 | g0136 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18970 | hp2 | a0002 | c0002 | t0017 | g0357 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18971 | hp1 | a0002 | c0007 | t0001 | g0022 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18975 | hp2 | a0001 | c0005 | t0004 | g0164 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18979 | hp1 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18979 | hp2 | a0001 | c0004 | t0001 | g0177 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18981 | hp2 | a0001 | c0004 | t0001 | g0007 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18984 | hp2 | a0001 | c0019 | t0001 | g0052 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18985 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18989 | hp1 | a0001 | c0004 | t0001 | g0225 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18990 | hp1 | a0001 | c0005 | t0004 | g0149 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18990 | hp2 | a0001 | c0004 | t0008 | g0029 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0018 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18993 | hp2 | a0001 | c0005 | t0004 | g0161 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18994 | hp2 | a0001 | c0005 | t0004 | g0162 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18995 | hp1 | a0003 | c0006 | t0001 | g0242 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18995 | hp2 | a0001 | c0018 | t0006 | g0308 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18997 | hp1 | a0006 | c0016 | t0002 | g0044 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18997 | hp2 | a0001 | c0005 | t0004 | g0147 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18999 | hp1 | a0001 | c0004 | t0001 | g0171 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0313 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0148 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0300 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19002 | hp2 | a0001 | c0005 | t0003 | g0103 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19004 | hp2 | a0003 | c0013 | t0001 | g0240 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0346 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19009 | hp2 | a0001 | c0005 | t0004 | g0130 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0274 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19012 | hp1 | a0001 | c0004 | t0001 | g0154 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0285 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19030 | hp1 | a0001 | c0012 | t0001 | g0091 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19030 | hp2 | a0001 | c0005 | t0005 | g0371 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19043 | hp1 | a0001 | c0005 | t0003 | g0260 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19043 | hp2 | a0001 | c0005 | t0021 | g0368 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19054 | hp1 | a0001 | c0005 | t0003 | g0089 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19054 | hp2 | a0001 | c0004 | t0001 | g0186 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19055 | hp2 | a0001 | c0005 | t0003 | g0102 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19056 | hp2 | a0001 | c0003 | t0001 | g0311 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19057 | hp2 | a0001 | c0005 | t0003 | g0104 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19060 | hp1 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19060 | hp2 | a0003 | c0006 | t0001 | g0238 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19063 | hp2 | a0001 | c0004 | t0001 | g0257 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19064 | hp1 | a0003 | c0006 | t0001 | g0241 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19064 | hp2 | a0003 | c0014 | t0001 | g0292 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0343 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19065 | hp2 | a0001 | c0003 | t0001 | g0277 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19068 | hp2 | a0003 | c0006 | t0001 | g0237 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19070 | hp1 | a0001 | c0004 | t0001 | g0041 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19070 | hp2 | a0001 | c0003 | t0001 | g0327 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19074 | hp1 | a0001 | c0003 | t0001 | g0201 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19074 | hp2 | a0003 | c0006 | t0001 | g0235 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19079 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19080 | hp1 | a0001 | c0003 | t0001 | g0278 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19082 | hp1 | a0001 | c0005 | t0004 | g0143 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0297 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19084 | hp2 | a0001 | c0004 | t0008 | g0028 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19085 | hp1 | a0001 | c0003 | t0001 | g0243 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19085 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19087 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19087 | hp2 | a0003 | c0006 | t0006 | g0181 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19088 | hp1 | a0001 | c0005 | t0004 | g0167 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19090 | hp1 | a0001 | c0004 | t0001 | g0061 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0275 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19240 | hp1 | a0001 | c0005 | t0003 | g0206 | AFR | YRI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0217 | AFR | YRI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0138 | AFR | ASW | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA20129 | hp2 | a0001 | c0004 | t0001 | g0134 | AFR | ASW | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0261 | EUR | TSI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0215 | EUR | TSI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA20805 | hp2 | a0001 | c0004 | t0001 | g0037 | EUR | TSI | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | GIH | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA20905 | hp2 | a0001 | c0004 | t0001 | g0050 | SAS | GIH | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0092 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | CLM | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0129 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02486 | hp1 | a0001 | c0004 | t0001 | g0121 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02486 | hp2 | a0001 | c0005 | t0010 | g0362 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03471 | hp1 | a0001 | c0004 | t0020 | g0359 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG06807 | hp1 | a0001 | c0003 | t0005 | g0378 | AFR | USA | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
HG06807 | hp2 | a0001 | c0005 | t0007 | g0267 | AFR | USA | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | USA | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA20300 | hp2 | a0001 | c0004 | t0001 | g0054 | AFR | USA | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA21309 | hp1 | a0002 | c0002 | t0012 | g0026 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0358 | REF | REF | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0189 | REF | REF | GFPT2_chr5_180295698_180358336 | GFPT2 | chr5 | 180295698 | 180358336 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:180313827 | T | C | 3 | a0002 a0004 a0006 |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
missense_variant | MODERATE | c.1411A>G | p.Ile471Val | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/19 | 1530/3034 | 1411/2049 | 471/682 | chr5 | 180313827 | |||
chr5:180313875 | T | G | 1 | a0003 | 18 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(15): Show |
missense_variant | MODERATE | c.1363A>C | p.Ile455Leu | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/19 | 1482/3034 | 1363/2049 | 455/682 | chr5 | 180313875 | |||
chr5:180316385 | G | T | 1 | a0004 | 2 | HG01261.hp1 HG01496.hp2 |
missense_variant | MODERATE | c.1229C>A | p.Thr410Lys | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/19 | 1348/3034 | 1229/2049 | 410/682 | chr5 | 180316385 | |||
chr5:180316994 | CATAGTAT others(3): Show |
C | 1 | a0006 | 1 | NA18997.hp1 | frameshift_variant | HIGH | c.1013_1022delTCAATA others(4): Show |
p.Phe338fs | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 11/19 | 1141/3034 | 1013/2049 | 338/682 | chr5 | 180316994 | |||
chr5:180318901 | C | T | 1 | a0005 | 2 | HG02965.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.850G>A | p.Ala284Thr | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/19 | 969/3034 | 850/2049 | 284/682 | chr5 | 180318901 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:180302429 | T | A | 1 | a0001c0019 | 1 | NA18984.hp2 | synonymous_variant | LOW | c.1998A>T | p.Gly666Gly | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/19 | 2117/3034 | 1998/2049 | 666/682 | chr5 | 180302429 | |||
chr5:180302519 | A | G | 16 | a0001c0003 a0001c0004 a0001c0005 others(13): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
synonymous_variant | LOW | c.1908T>C | p.Ile636Ile | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/19 | 2027/3034 | 1908/2049 | 636/682 | chr5 | 180302519 | |||
chr5:180307200 | A | G | 9 | a0001c0004 a0001c0012 a0001c0018 others(6): Show |
86 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
synonymous_variant | LOW | c.1650T>C | p.Tyr550Tyr | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/19 | 1769/3034 | 1650/2049 | 550/682 | chr5 | 180307200 | |||
chr5:180307230 | C | G | 3 | a0001c0018 a0003c0006 a0003c0013 |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
synonymous_variant | LOW | c.1620G>C | p.Ser540Ser | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/19 | 1739/3034 | 1620/2049 | 540/682 | chr5 | 180307230 | |||
chr5:180313954 | C | T | 1 | a0001c0017 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1284G>A | p.Ala428Ala | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/19 | 1403/3034 | 1284/2049 | 428/682 | chr5 | 180313954 | |||
chr5:180317009 | T | G | 4 | a0001c0003 a0002c0020 a0003c0013 others(1): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
synonymous_variant | LOW | c.1008A>C | p.Ser336Ser | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 11/19 | 1127/3034 | 1008/2049 | 336/682 | chr5 | 180317009 | |||
chr5:180318854 | G | A | 2 | a0001c0009 a0001c0021 |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.897C>T | p.Ala299Ala | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/19 | 1016/3034 | 897/2049 | 299/682 | chr5 | 180318854 | |||
chr5:180338506 | G | A | 1 | a0002c0015 | 2 | HG02896.hp1 HG02897.hp1 |
synonymous_variant | LOW | c.102C>T | p.Gly34Gly | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/19 | 221/3034 | 102/2049 | 34/682 | chr5 | 180338506 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:180300706 | A | G | 3 | a0001c0003t0004 a0001c0005t0004 a0002c0002t0004 |
24 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*858T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 858 | chr5 | 180300706 | ||||||
chr5:180300804 | A | C | 4 | a0001c0004t0003 a0001c0005t0003 a0001c0005t0011 others(1): Show |
28 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*760T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 760 | chr5 | 180300804 | ||||||
chr5:180300872 | G | A | 1 | a0001c0005t0015 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*692C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 692 | chr5 | 180300872 | ||||||
chr5:180300957 | C | T | 7 | a0001c0005t0002 a0002c0002t0002 a0002c0002t0012 others(4): Show |
88 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*607G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 607 | chr5 | 180300957 | ||||||
chr5:180300975 | T | C | 1 | a0001c0004t0016 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*589A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 589 | chr5 | 180300975 | ||||||
chr5:180300988 | G | A | 3 | a0001c0003t0004 a0001c0005t0004 a0002c0002t0004 |
24 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*576C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 576 | chr5 | 180300988 | ||||||
chr5:180301000 | G | A | 2 | a0001c0018t0006 a0003c0006t0006 |
4 | NA18959.hp1 NA18970.hp1 NA18995.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*564C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 564 | chr5 | 180301000 | ||||||
chr5:180301010 | G | T | 1 | a0001c0004t0016 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*554C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 554 | chr5 | 180301010 | ||||||
chr5:180301328 | C | G | 4 | a0001c0005t0007 a0001c0005t0010 a0001c0005t0015 others(1): Show |
7 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*236G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 236 | chr5 | 180301328 | ||||||
chr5:180301368 | C | T | 1 | a0001c0003t0014 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 196 | chr5 | 180301368 | ||||||
chr5:180301552 | A | G | 1 | a0001c0001t0009 | 2 | HG03195.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*12T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 19/19 | 12 | chr5 | 180301552 | ||||||
chr5:180353263 | G | A | 1 | a0002c0002t0017 | 1 | NA18970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | chr5 | 180353263 | |||||||
chr5:180353274 | G | GGGGCTCC others(5): Show |
1 | a0001c0004t0008 | 2 | NA18990.hp2 NA19084.hp2 |
5_prime_UTR_variant | MODIFIER | c.-69_-58dupACGGAGGA others(4): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 58 | chr5 | 180353274 | ||||||
chr5:180353280 | CCTCCGTG others(14): Show |
C | 3 | a0001c0004t0020 a0001c0005t0010 a0001c0005t0019 |
4 | HG02486.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-84_-64delCCCACGGA others(13): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 64 | chr5 | 180353280 | ||||||
chr5:180353292 | CCTCCGTG others(2): Show |
C | 28 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(25): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
5_prime_UTR_variant | MODIFIER | c.-84_-76delCCCACGGA others(1): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 76 | chr5 | 180353292 | ||||||
chr5:180353296 | C | T | 6 | a0001c0001t0001 a0001c0003t0001 a0001c0004t0001 others(3): Show |
29 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-79G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 79 | chr5 | 180353296 | ||||||
chr5:180353305 | C | T | 1 | a0002c0002t0013 | 1 | HG03710.hp2 | 5_prime_UTR_variant | MODIFIER | c.-88G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 88 | chr5 | 180353305 | ||||||
chr5:180353307 | TGGGCTCC others(11): Show |
T | 1 | a0002c0002t0012 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-108_-91delGCGGAGC others(11): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 91 | chr5 | 180353307 | ||||||
chr5:180353310 | G | T | 1 | a0001c0001t0001 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-93C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 93 | chr5 | 180353310 | ||||||
chr5:180353328 | G | A | 7 | a0001c0001t0005 a0001c0003t0005 a0001c0004t0005 others(4): Show |
19 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-111C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/19 | 111 | chr5 | 180353328 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:180301707 | T | C | 164 | a0001c0003t0001g0203 a0001c0003t0001g0277 a0001c0003t0001g0314 others(161): Show |
175 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.2005-99A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301707 | |||||||
chr5:180301849 | T | C | 74 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(71): Show |
79 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.2005-241A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301849 | |||||||
chr5:180301860 | A | C | 163 | a0001c0003t0001g0277 a0001c0003t0001g0314 a0001c0003t0004g0119 others(160): Show |
174 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.2005-252T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301860 | |||||||
chr5:180301930 | T | C | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.2005-322A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301930 | |||||||
chr5:180301936 | T | C | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.2005-328A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301936 | |||||||
chr5:180301998 | C | G | 111 | a0001c0003t0004g0119 a0001c0005t0002g0082 a0001c0005t0002g0107 others(108): Show |
119 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.2005-390G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180301998 | |||||||
chr5:180302009 | G | A | 126 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(123): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.2005-401C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302009 | |||||||
chr5:180302018 | C | CGGTGGCT others(1694): Show |
1 | a0001c0003t0001g0200 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2004+404_2004+405i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302018 | |||||||
chr5:180302029 | A | ACCTGTAA others(1693): Show |
1 | a0001c0005t0004g0058 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1702): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
1 | a0002c0002t0002g0032 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
18 | a0001c0003t0004g0119 a0001c0005t0004g0045 a0001c0005t0004g0130 others(15): Show |
18 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
79 | a0001c0005t0002g0082 a0001c0005t0002g0107 a0002c0002t0002g0003 others(76): Show |
87 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1693): Show |
2 | a0001c0005t0004g0161 a0001c0005t0004g0167 |
2 | NA18993.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1702): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
7 | a0001c0005t0007g0267 a0001c0005t0007g0304 a0001c0005t0007g0353 others(4): Show |
7 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
1 | a0002c0002t0017g0357 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1695): Show |
1 | a0002c0002t0002g0155 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1704): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1691): Show |
1 | a0001c0005t0004g0149 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1700): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
1 | a0001c0003t0005g0378 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
1 | a0001c0005t0005g0371 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
1 | a0001c0004t0008g0029 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
3 | a0001c0004t0020g0359 a0005c0010t0001g0132 a0005c0010t0001g0133 |
3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1693): Show |
2 | a0001c0004t0001g0224 a0001c0004t0001g0227 |
2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1702): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
46 | a0001c0003t0001g0277 a0001c0004t0001g0007 a0001c0004t0001g0014 others(43): Show |
49 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1693): Show |
1 | a0001c0003t0001g0093 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1702): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
1 | a0001c0003t0001g0347 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
1 | a0001c0003t0001g0335 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
1 | a0003c0014t0001g0292 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
60 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(57): Show |
65 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
1 | a0001c0003t0001g0243 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
1 | a0001c0003t0014g0336 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1695): Show |
1 | a0001c0003t0001g0252 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2004+393_2004+394i others(1704): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302029 | A | ACCTGTAA others(1694): Show |
4 | a0001c0005t0001g0341 a0001c0009t0001g0180 a0001c0009t0001g0356 others(1): Show |
4 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004+393_2004+394i others(1703): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302029 | |||||||
chr5:180302062 | A | G | 236 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(233): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.2004+361T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302062 | |||||||
chr5:180302085 | A | T | 3 | a0001c0001t0005g0369 a0001c0001t0005g0372 a0001c0001t0005g0376 |
3 | HG02015.hp1 HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2004+338T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302085 | |||||||
chr5:180302104 | G | A | 5 | a0001c0005t0001g0341 a0001c0009t0001g0180 a0001c0009t0001g0356 others(2): Show |
5 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004+319C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302104 | |||||||
chr5:180302115 | G | A | 5 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(2): Show |
5 | HG02630.hp1 HG02647.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2004+308C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302115 | |||||||
chr5:180302167 | G | A | 3 | a0001c0005t0003g0283 a0002c0002t0004g0025 a0002c0002t0004g0349 |
4 | HG01099.hp1 HG01928.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+256C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302167 | |||||||
chr5:180302201 | C | T | 5 | a0001c0005t0003g0033 a0001c0005t0003g0088 a0001c0005t0003g0265 others(2): Show |
5 | HG02717.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2004+222G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302201 | |||||||
chr5:180302283 | T | A | 75 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(72): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.2004+140A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302283 | |||||||
chr5:180302286 | CA | C | 7 | a0001c0001t0001g0099 a0001c0003t0001g0301 a0001c0004t0001g0227 others(4): Show |
7 | HG00558.hp2 HG01517.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004+136delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302286 | |||||||
chr5:180302286 | CAA | C | 110 | a0001c0003t0004g0119 a0001c0005t0002g0082 a0001c0005t0002g0107 others(107): Show |
118 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.2004+135_2004+136d others(4): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302286 | |||||||
chr5:180302328 | C | T | 237 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(234): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.2004+95G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302328 | |||||||
chr5:180302391 | T | C | 15 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(12): Show |
16 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(13): Show |
intron_variant | MODIFIER | c.2004+32A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 18/18 | chr5 | 180302391 | |||||||
chr5:180302625 | A | G | 111 | a0001c0003t0004g0119 a0001c0005t0002g0082 a0001c0005t0002g0107 others(108): Show |
119 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1843-41T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180302625 | |||||||
chr5:180302853 | G | A | 1 | a0001c0005t0003g0283 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1843-269C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180302853 | |||||||
chr5:180302967 | C | T | 69 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(66): Show |
74 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1843-383G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180302967 | |||||||
chr5:180303004 | T | C | 295 | a0001c0001t0005g0363 a0001c0001t0005g0364 a0001c0003t0001g0002 others(292): Show |
313 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1843-420A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303004 | |||||||
chr5:180303045 | T | C | 72 | a0001c0001t0005g0380 a0001c0001t0005g0381 a0001c0003t0004g0119 others(69): Show |
75 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1843-461A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303045 | |||||||
chr5:180303056 | T | C | 52 | a0001c0004t0001g0007 a0001c0004t0001g0014 a0001c0004t0001g0015 others(49): Show |
55 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1843-472A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303056 | |||||||
chr5:180303065 | TA | T | 51 | a0001c0004t0001g0007 a0001c0004t0001g0014 a0001c0004t0001g0015 others(48): Show |
54 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1843-482delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303065 | |||||||
chr5:180303082 | T | G | 50 | a0001c0004t0001g0007 a0001c0004t0001g0014 a0001c0004t0001g0015 others(47): Show |
53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1843-498A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303082 | |||||||
chr5:180303090 | T | C | 58 | a0001c0001t0001g0115 a0001c0004t0001g0007 a0001c0004t0001g0014 others(55): Show |
61 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1843-506A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303090 | |||||||
chr5:180303092 | T | C | 50 | a0001c0004t0001g0007 a0001c0004t0001g0014 a0001c0004t0001g0015 others(47): Show |
53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1843-508A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303092 | |||||||
chr5:180303102 | G | C | 87 | a0001c0001t0005g0377 a0001c0003t0001g0175 a0001c0003t0004g0119 others(84): Show |
90 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1843-518C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303102 | |||||||
chr5:180303103 | G | A | 1 | a0001c0001t0005g0377 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1843-519C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303103 | |||||||
chr5:180303122 | G | C | 77 | a0001c0003t0004g0119 a0001c0004t0001g0007 a0001c0004t0001g0014 others(74): Show |
80 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1843-538C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303122 | |||||||
chr5:180303184 | G | T | 183 | a0001c0003t0004g0119 a0001c0004t0001g0007 a0001c0004t0001g0014 others(180): Show |
194 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.1843-600C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303184 | |||||||
chr5:180303217 | C | G | 27 | a0001c0005t0003g0033 a0001c0005t0003g0088 a0001c0005t0003g0089 others(24): Show |
27 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1843-633G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303217 | |||||||
chr5:180303220 | A | G | 2 | a0001c0001t0005g0365 a0001c0001t0005g0367 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1843-636T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303220 | |||||||
chr5:180303221 | C | T | 20 | a0001c0003t0004g0119 a0001c0005t0004g0045 a0001c0005t0004g0058 others(17): Show |
20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1843-637G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303221 | |||||||
chr5:180303224 | C | A | 27 | a0001c0005t0003g0033 a0001c0005t0003g0088 a0001c0005t0003g0089 others(24): Show |
27 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1843-640G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303224 | |||||||
chr5:180303225 | G | A | 28 | a0001c0001t0001g0338 a0001c0005t0003g0033 a0001c0005t0003g0088 others(25): Show |
28 | HG01167.hp2 HG01358.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1843-641C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303225 | |||||||
chr5:180303228 | A | T | 27 | a0001c0005t0003g0033 a0001c0005t0003g0088 a0001c0005t0003g0089 others(24): Show |
27 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1843-644T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303228 | |||||||
chr5:180303229 | CA | C | 184 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(181): Show |
194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1843-646delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303229 | |||||||
chr5:180303232 | A | C | 2 | a0001c0004t0001g0005 a0001c0004t0001g0197 |
3 | HG01952.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1843-648T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303232 | |||||||
chr5:180303234 | A | C | 2 | a0001c0004t0001g0005 a0001c0004t0001g0197 |
3 | HG01952.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1843-650T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303234 | |||||||
chr5:180303236 | A | C | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1843-652T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303236 | |||||||
chr5:180303380 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1843-796C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303380 | |||||||
chr5:180303426 | G | A | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1843-842C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303426 | |||||||
chr5:180303432 | G | T | 2 | a0002c0002t0004g0025 a0002c0002t0004g0349 |
3 | HG01099.hp1 HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1843-848C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303432 | |||||||
chr5:180303460 | A | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(40): Show |
50 | HG00280.hp1 HG01255.hp1 HG01258.hp1 others(47): Show |
intron_variant | MODIFIER | c.1843-876T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303460 | |||||||
chr5:180303478 | A | G | 48 | a0001c0001t0001g0338 a0001c0004t0001g0007 a0001c0004t0001g0014 others(45): Show |
51 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1843-894T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303478 | |||||||
chr5:180303700 | C | G | 1 | a0001c0003t0001g0311 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1842+1072G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303700 | |||||||
chr5:180303843 | A | G | 238 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(235): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1842+929T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303843 | |||||||
chr5:180303938 | T | C | 114 | a0001c0003t0004g0119 a0001c0004t0020g0359 a0001c0005t0002g0082 others(111): Show |
122 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1842+834A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180303938 | |||||||
chr5:180304014 | T | C | 238 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(235): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1842+758A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304014 | |||||||
chr5:180304053 | A | C | 1 | a0001c0001t0001g0326 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1842+719T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304053 | |||||||
chr5:180304113 | G | A | 84 | a0001c0005t0002g0082 a0001c0005t0002g0107 a0002c0002t0002g0003 others(81): Show |
92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1842+659C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304113 | |||||||
chr5:180304135 | G | A | 1 | a0001c0003t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1842+637C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304135 | |||||||
chr5:180304297 | G | T | 84 | a0001c0005t0002g0082 a0001c0005t0002g0107 a0002c0002t0002g0003 others(81): Show |
92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1842+475C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304297 | |||||||
chr5:180304328 | T | G | 84 | a0001c0005t0002g0082 a0001c0005t0002g0107 a0002c0002t0002g0003 others(81): Show |
92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1842+444A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304328 | |||||||
chr5:180304363 | C | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0176 a0001c0001t0001g0342 |
3 | HG02818.hp1 HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1842+409G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304363 | |||||||
chr5:180304377 | G | A | 236 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(233): Show |
252 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.1842+395C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304377 | |||||||
chr5:180304412 | A | G | 1 | a0001c0005t0005g0371 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1842+360T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304412 | |||||||
chr5:180304433 | G | A | 1 | a0001c0005t0003g0103 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1842+339C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304433 | |||||||
chr5:180304466 | C | A | 127 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(124): Show |
135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1842+306G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304466 | |||||||
chr5:180304575 | G | T | 1 | a0001c0004t0001g0037 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1842+197C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304575 | |||||||
chr5:180304635 | C | G | 238 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(235): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1842+137G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304635 | |||||||
chr5:180304695 | C | T | 127 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(124): Show |
135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1842+77G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304695 | |||||||
chr5:180304715 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1842+57C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 17/18 | chr5 | 180304715 | |||||||
chr5:180305126 | C | T | 2 | a0002c0002t0002g0047 a0002c0002t0002g0048 |
2 | NA18945.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1675-187G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305126 | |||||||
chr5:180305221 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1675-282C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305221 | |||||||
chr5:180305240 | C | A | 111 | a0001c0003t0004g0119 a0001c0005t0002g0082 a0001c0005t0002g0107 others(108): Show |
119 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1675-301G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305240 | |||||||
chr5:180305350 | A | G | 265 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(262): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.1675-411T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305350 | |||||||
chr5:180305426 | T | C | 1 | a0001c0003t0001g0303 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1675-487A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305426 | |||||||
chr5:180305441 | C | T | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1675-502G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305441 | |||||||
chr5:180305447 | G | A | 1 | a0001c0012t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1675-508C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305447 | |||||||
chr5:180305604 | C | T | 1 | a0001c0005t0003g0283 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1675-665G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305604 | |||||||
chr5:180305655 | C | T | 1 | a0001c0005t0003g0283 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1675-716G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305655 | |||||||
chr5:180305678 | T | G | 238 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(235): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1675-739A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305678 | |||||||
chr5:180305680 | C | A | 19 | a0001c0003t0004g0119 a0001c0005t0004g0045 a0001c0005t0004g0058 others(16): Show |
19 | HG00609.hp1 HG00673.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1675-741G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305680 | |||||||
chr5:180305680 | C | T | 50 | a0001c0004t0001g0007 a0001c0004t0001g0014 a0001c0004t0001g0015 others(47): Show |
53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1675-741G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305680 | |||||||
chr5:180305741 | C | T | 17 | a0001c0005t0004g0045 a0001c0005t0004g0058 a0001c0005t0004g0130 others(14): Show |
17 | HG00609.hp1 HG00673.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1675-802G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305741 | |||||||
chr5:180305771 | A | G | 128 | a0001c0001t0001g0329 a0001c0003t0001g0002 a0001c0003t0001g0018 others(125): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1675-832T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305771 | |||||||
chr5:180305797 | C | T | 127 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(124): Show |
135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1675-858G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305797 | |||||||
chr5:180305974 | T | G | 111 | a0001c0003t0004g0119 a0001c0005t0002g0082 a0001c0005t0002g0107 others(108): Show |
119 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1675-1035A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305974 | |||||||
chr5:180305983 | CT | C | 215 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(212): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1675-1045delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305983 | |||||||
chr5:180305986 | T | C | 3 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0004t0001g0344 |
3 | HG02630.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1675-1047A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305986 | |||||||
chr5:180305987 | T | C | 1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1675-1048A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180305987 | |||||||
chr5:180306016 | G | A | 1 | a0001c0005t0003g0283 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1675-1077C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306016 | |||||||
chr5:180306193 | C | T | 1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1674+983G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306193 | |||||||
chr5:180306372 | G | A | 1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1674+804C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306372 | |||||||
chr5:180306407 | C | T | 267 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(264): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.1674+769G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306407 | |||||||
chr5:180306413 | G | T | 7 | a0001c0005t0007g0267 a0001c0005t0007g0304 a0001c0005t0007g0353 others(4): Show |
7 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+763C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306413 | |||||||
chr5:180306440 | T | C | 267 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(264): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.1674+736A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306440 | |||||||
chr5:180306447 | A | G | 20 | a0001c0003t0004g0119 a0001c0005t0004g0045 a0001c0005t0004g0058 others(17): Show |
20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1674+729T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306447 | |||||||
chr5:180306466 | C | T | 2 | a0001c0004t0001g0005 a0001c0004t0001g0197 |
3 | HG01952.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1674+710G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306466 | |||||||
chr5:180306481 | T | C | 1 | a0001c0004t0001g0188 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1674+695A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306481 | |||||||
chr5:180306515 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1674+661C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306515 | |||||||
chr5:180306551 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1674+625G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306551 | |||||||
chr5:180306691 | C | T | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1674+485G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306691 | |||||||
chr5:180306707 | C | A | 17 | a0001c0005t0004g0045 a0001c0005t0004g0058 a0001c0005t0004g0130 others(14): Show |
17 | HG00609.hp1 HG00673.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1674+469G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306707 | |||||||
chr5:180306727 | G | A | 1 | a0001c0009t0005g0375 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1674+449C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306727 | |||||||
chr5:180306735 | C | G | 1 | a0001c0005t0003g0283 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1674+441G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306735 | |||||||
chr5:180306789 | G | C | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1674+387C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306789 | |||||||
chr5:180306865 | T | G | 1 | a0001c0005t0007g0353 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1674+311A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306865 | |||||||
chr5:180306916 | C | T | 7 | a0001c0005t0007g0267 a0001c0005t0007g0304 a0001c0005t0007g0353 others(4): Show |
7 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+260G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306916 | |||||||
chr5:180306928 | G | A | 7 | a0001c0004t0001g0223 a0001c0004t0001g0224 a0001c0004t0001g0225 others(4): Show |
7 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+248C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306928 | |||||||
chr5:180306934 | T | C | 267 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(264): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.1674+242A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306934 | |||||||
chr5:180306943 | C | T | 1 | a0002c0002t0004g0349 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1674+233G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306943 | |||||||
chr5:180306961 | T | A | 3 | a0001c0004t0020g0359 a0005c0010t0001g0132 a0005c0010t0001g0133 |
3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1674+215A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180306961 | |||||||
chr5:180307037 | C | T | 7 | a0001c0005t0007g0267 a0001c0005t0007g0304 a0001c0005t0007g0353 others(4): Show |
7 | HG02257.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674+139G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307037 | |||||||
chr5:180307075 | G | A | 22 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0005g0366 others(19): Show |
23 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.1674+101C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307075 | |||||||
chr5:180307084 | C | T | 27 | a0001c0004t0001g0134 a0001c0004t0001g0195 a0001c0004t0001g0204 others(24): Show |
28 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1674+92G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307084 | |||||||
chr5:180307092 | A | G | 2 | a0005c0010t0001g0132 a0005c0010t0001g0133 |
2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1674+84T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307092 | |||||||
chr5:180307110 | C | A | 27 | a0001c0004t0001g0134 a0001c0004t0001g0195 a0001c0004t0001g0204 others(24): Show |
28 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1674+66G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307110 | |||||||
chr5:180307139 | T | C | 118 | a0001c0004t0001g0134 a0001c0004t0001g0195 a0001c0004t0001g0204 others(115): Show |
127 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.1674+37A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307139 | |||||||
chr5:180307145 | GTGGGGGT others(6): Show |
G | 111 | a0001c0004t0001g0134 a0001c0004t0001g0195 a0001c0004t0001g0204 others(108): Show |
120 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1674+18_1674+30del others(13): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 16/18 | chr5 | 180307145 | |||||||
chr5:180307312 | T | C | 83 | a0001c0005t0002g0107 a0002c0002t0002g0003 a0002c0002t0002g0006 others(80): Show |
91 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1547-9A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307312 | |||||||
chr5:180307326 | G | A | 1 | a0001c0005t0004g0163 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1547-23C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307326 | |||||||
chr5:180307373 | A | AT | 20 | a0001c0005t0003g0089 a0001c0005t0003g0102 a0001c0005t0003g0103 others(17): Show |
20 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1547-71dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307373 | |||||||
chr5:180307528 | A | C | 127 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(124): Show |
135 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1547-225T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307528 | |||||||
chr5:180307587 | CAG | C | 74 | a0001c0001t0001g0307 a0001c0003t0001g0002 a0001c0003t0001g0018 others(71): Show |
79 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.1547-286_1547-285d others(4): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307587 | |||||||
chr5:180307591 | G | C | 1 | a0002c0002t0002g0106 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1547-288C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307591 | |||||||
chr5:180307637 | C | T | 1 | a0001c0004t0001g0056 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1547-334G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307637 | |||||||
chr5:180307827 | T | G | 6 | a0002c0002t0002g0006 a0002c0002t0002g0040 a0002c0002t0002g0139 others(3): Show |
7 | NA18970.hp2 NA18971.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.1547-524A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307827 | |||||||
chr5:180307884 | G | A | 51 | a0001c0004t0001g0007 a0001c0004t0001g0014 a0001c0004t0001g0015 others(48): Show |
54 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.1547-581C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307884 | |||||||
chr5:180307928 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0099 others(3): Show |
10 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1547-625A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307928 | |||||||
chr5:180307969 | G | T | 1 | a0001c0021t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1547-666C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307969 | |||||||
chr5:180307978 | T | C | 25 | a0001c0004t0001g0134 a0001c0004t0001g0204 a0001c0004t0001g0217 others(22): Show |
26 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.1547-675A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180307978 | |||||||
chr5:180308031 | C | T | 48 | a0001c0001t0001g0122 a0001c0004t0001g0007 a0001c0004t0001g0014 others(45): Show |
51 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1547-728G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308031 | |||||||
chr5:180308038 | C | T | 25 | a0001c0004t0001g0134 a0001c0004t0001g0204 a0001c0004t0001g0217 others(22): Show |
26 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.1547-735G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308038 | |||||||
chr5:180308078 | G | A | 284 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(281): Show |
307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1547-775C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308078 | |||||||
chr5:180308113 | G | A | 72 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(69): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1547-810C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308113 | |||||||
chr5:180308124 | C | T | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-821G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308124 | |||||||
chr5:180308129 | G | A | 26 | a0001c0004t0001g0134 a0001c0004t0001g0195 a0001c0004t0001g0204 others(23): Show |
27 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.1547-826C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308129 | |||||||
chr5:180308168 | G | A | 1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1547-865C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308168 | |||||||
chr5:180308188 | G | A | 3 | a0001c0004t0001g0134 a0001c0004t0001g0270 a0001c0004t0001g0344 |
3 | HG02647.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1547-885C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308188 | |||||||
chr5:180308204 | T | C | 1 | a0001c0021t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1547-901A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308204 | |||||||
chr5:180308213 | A | G | 111 | a0001c0004t0001g0134 a0001c0004t0001g0195 a0001c0004t0001g0204 others(108): Show |
120 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1547-910T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308213 | |||||||
chr5:180308217 | C | T | 6 | a0001c0004t0001g0007 a0001c0004t0001g0060 a0001c0004t0001g0068 others(3): Show |
7 | HG00438.hp2 HG02040.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1547-914G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308217 | |||||||
chr5:180308255 | C | CA | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-953_1547-952i others(3): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308255 | |||||||
chr5:180308256 | G | A | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-953C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308256 | |||||||
chr5:180308256 | G | GA | 11 | a0001c0004t0001g0134 a0001c0004t0001g0195 a0001c0004t0001g0204 others(8): Show |
11 | HG02451.hp1 HG02630.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1547-954dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308256 | |||||||
chr5:180308269 | G | A | 1 | a0002c0002t0002g0074 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1547-966C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308269 | |||||||
chr5:180308270 | A | G | 1 | a0002c0002t0002g0074 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1547-967T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308270 | |||||||
chr5:180308359 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(126): Show |
142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-1056G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308359 | |||||||
chr5:180308366 | G | A | 19 | a0001c0005t0004g0045 a0001c0005t0004g0058 a0001c0005t0004g0130 others(16): Show |
19 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1547-1063C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308366 | |||||||
chr5:180308449 | A | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(153): Show |
170 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1547-1146T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308449 | |||||||
chr5:180308547 | C | T | 30 | a0001c0001t0001g0284 a0001c0001t0009g0290 a0001c0005t0001g0219 others(27): Show |
30 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1547-1244G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308547 | |||||||
chr5:180308548 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(126): Show |
142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-1245C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308548 | |||||||
chr5:180308674 | A | G | 76 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(73): Show |
81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1547-1371T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308674 | |||||||
chr5:180308695 | A | T | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-1392T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308695 | |||||||
chr5:180308763 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(126): Show |
142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-1460A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308763 | |||||||
chr5:180308792 | C | A | 19 | a0001c0005t0004g0045 a0001c0005t0004g0058 a0001c0005t0004g0130 others(16): Show |
19 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1547-1489G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308792 | |||||||
chr5:180308873 | C | CT | 105 | a0001c0003t0001g0243 a0001c0003t0005g0378 a0001c0004t0001g0134 others(102): Show |
113 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.1547-1571dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308873 | |||||||
chr5:180308873 | C | CTT | 6 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0005g0366 others(3): Show |
6 | HG02056.hp2 HG02451.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1547-1572_1547-157 others(6): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308873 | |||||||
chr5:180308898 | C | G | 27 | a0001c0004t0001g0134 a0001c0004t0001g0195 a0001c0004t0001g0204 others(24): Show |
28 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1547-1595G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308898 | |||||||
chr5:180308910 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(23): Show |
31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1547-1607G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308910 | |||||||
chr5:180308941 | C | A | 9 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0071 others(6): Show |
11 | HG00438.hp1 HG00597.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1547-1638G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308941 | |||||||
chr5:180308954 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(126): Show |
142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-1651G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308954 | |||||||
chr5:180308959 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(155): Show |
173 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.1547-1656T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180308959 | |||||||
chr5:180309043 | T | A | 1 | a0001c0001t0001g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1547-1740A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309043 | |||||||
chr5:180309123 | C | T | 22 | a0001c0004t0020g0359 a0001c0005t0004g0045 a0001c0005t0004g0058 others(19): Show |
22 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.1547-1820G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309123 | |||||||
chr5:180309193 | A | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(153): Show |
170 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.1547-1890T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309193 | |||||||
chr5:180309224 | G | A | 1 | a0002c0002t0002g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1547-1921C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309224 | |||||||
chr5:180309341 | A | C | 1 | a0001c0003t0001g0030 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1547-2038T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309341 | |||||||
chr5:180309367 | A | G | 103 | a0001c0005t0002g0082 a0001c0005t0002g0107 a0001c0005t0004g0045 others(100): Show |
111 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1547-2064T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309367 | |||||||
chr5:180309414 | G | C | 1 | a0001c0009t0001g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1547-2111C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309414 | |||||||
chr5:180309454 | CTT | C | 84 | a0001c0005t0002g0082 a0001c0005t0002g0107 a0002c0002t0002g0003 others(81): Show |
92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1547-2153_1547-215 others(6): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309454 | |||||||
chr5:180309483 | T | G | 1 | a0003c0006t0006g0181 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1547-2180A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309483 | |||||||
chr5:180309512 | C | T | 2 | a0001c0001t0001g0284 a0001c0005t0019g0361 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1547-2209G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309512 | |||||||
chr5:180309613 | C | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(311): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.1547-2310G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309613 | |||||||
chr5:180309631 | C | T | 1 | a0001c0004t0001g0344 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1547-2328G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309631 | |||||||
chr5:180309657 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(126): Show |
142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-2354A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309657 | |||||||
chr5:180309742 | T | C | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-2439A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309742 | |||||||
chr5:180309755 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(126): Show |
142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1547-2452C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309755 | |||||||
chr5:180309816 | C | CT | 29 | a0001c0001t0001g0334 a0001c0001t0009g0290 a0001c0005t0001g0219 others(26): Show |
29 | HG01123.hp2 HG01167.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1547-2514dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309816 | |||||||
chr5:180309839 | A | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(252): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1547-2536T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309839 | |||||||
chr5:180309842 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(252): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1547-2539T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309842 | |||||||
chr5:180309936 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(252): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1546+2494C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309936 | |||||||
chr5:180309959 | C | T | 1 | a0001c0004t0001g0188 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1546+2471G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309959 | |||||||
chr5:180309960 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(127): Show |
143 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1546+2470T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309960 | |||||||
chr5:180309967 | C | T | 4 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+2463G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180309967 | |||||||
chr5:180310000 | C | T | 2 | a0002c0002t0002g0038 a0002c0002t0002g0039 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1546+2430G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310000 | |||||||
chr5:180310012 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(252): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.1546+2418T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310012 | |||||||
chr5:180310032 | G | A | 1 | a0001c0004t0001g0055 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1546+2398C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310032 | |||||||
chr5:180310104 | C | T | 20 | a0001c0005t0004g0045 a0001c0005t0004g0058 a0001c0005t0004g0130 others(17): Show |
20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1546+2326G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310104 | |||||||
chr5:180310106 | A | G | 314 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(311): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.1546+2324T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310106 | |||||||
chr5:180310125 | G | A | 1 | a0001c0001t0005g0369 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1546+2305C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310125 | |||||||
chr5:180310141 | C | T | 2 | a0003c0006t0001g0017 a0003c0006t0001g0244 |
3 | HG00099.hp1 HG03239.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1546+2289G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310141 | |||||||
chr5:180310256 | G | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(281): Show |
307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1546+2174C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310256 | |||||||
chr5:180310560 | G | A | 2 | a0001c0004t0001g0217 a0001c0004t0001g0218 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1546+1870C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310560 | |||||||
chr5:180310630 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(23): Show |
31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1546+1800G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310630 | |||||||
chr5:180310659 | C | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(126): Show |
142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1546+1771G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310659 | |||||||
chr5:180310698 | ACCGCG | A | 27 | a0001c0004t0001g0134 a0001c0004t0001g0195 a0001c0004t0001g0204 others(24): Show |
28 | HG00099.hp1 HG01975.hp1 HG02451.hp1 others(25): Show |
intron_variant | MODIFIER | c.1546+1727_1546+173 others(9): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310698 | |||||||
chr5:180310738 | G | T | 1 | a0001c0012t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1546+1692C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310738 | |||||||
chr5:180310756 | C | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(107): Show |
123 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1546+1674G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310756 | |||||||
chr5:180310793 | G | A | 3 | a0001c0004t0020g0359 a0005c0010t0001g0132 a0005c0010t0001g0133 |
3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1546+1637C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310793 | |||||||
chr5:180310832 | C | CA | 46 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0069 others(43): Show |
48 | HG00099.hp2 HG00323.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1546+1597dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | C | CAA | 37 | a0001c0001t0001g0332 a0001c0001t0005g0376 a0001c0005t0003g0033 others(34): Show |
42 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1546+1596_1546+159 others(6): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | C | CAAA | 39 | a0001c0001t0005g0372 a0001c0005t0002g0107 a0001c0005t0003g0172 others(36): Show |
42 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1546+1595_1546+159 others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | C | CAAAA | 9 | a0001c0005t0002g0082 a0002c0002t0002g0048 a0002c0002t0002g0106 others(6): Show |
9 | HG01257.hp1 HG01358.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1546+1594_1546+159 others(8): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | CA | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0099 a0001c0001t0001g0193 others(22): Show |
28 | HG00609.hp1 HG00642.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.1546+1597delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | CAA | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0100 others(17): Show |
21 | HG01258.hp1 HG01515.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1546+1596_1546+159 others(6): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | CAAA | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0208 a0001c0004t0001g0053 others(3): Show |
7 | HG01884.hp2 HG02055.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546+1595_1546+159 others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | CAAAA | C | 52 | a0001c0003t0001g0020 a0001c0003t0001g0064 a0001c0003t0001g0065 others(49): Show |
56 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1546+1594_1546+159 others(8): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | CAAAAA | C | 61 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0030 others(58): Show |
65 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1546+1593_1546+159 others(9): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | CAAAAAA | C | 9 | a0001c0003t0001g0031 a0001c0003t0001g0230 a0001c0003t0001g0288 others(6): Show |
9 | HG00140.hp1 HG01192.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546+1592_1546+159 others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | CAAAAAAA others(2): Show |
C | 11 | a0003c0006t0001g0017 a0003c0006t0001g0236 a0003c0006t0001g0237 others(8): Show |
12 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.1546+1589_1546+159 others(13): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | CAAAAAAA others(3): Show |
C | 1 | a0003c0006t0001g0235 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1546+1588_1546+159 others(14): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310832 | CAAAAAAA others(5): Show |
C | 3 | a0001c0004t0001g0005 a0001c0004t0001g0197 a0002c0002t0002g0222 |
4 | HG01952.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546+1586_1546+159 others(16): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310832 | |||||||
chr5:180310863 | A | T | 2 | a0001c0004t0001g0005 a0001c0004t0001g0197 |
3 | HG01952.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1546+1567T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310863 | |||||||
chr5:180310864 | A | T | 2 | a0001c0003t0001g0198 a0001c0003t0001g0305 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1546+1566T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310864 | |||||||
chr5:180310865 | T | A | 9 | a0001c0005t0003g0206 a0001c0005t0003g0207 a0001c0005t0003g0209 others(6): Show |
9 | HG01167.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1546+1565A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310865 | |||||||
chr5:180310873 | A | G | 3 | a0001c0001t0001g0264 a0001c0001t0001g0323 a0001c0001t0001g0328 |
3 | HG01099.hp2 HG01934.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1546+1557T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310873 | |||||||
chr5:180310891 | T | C | 50 | a0001c0004t0001g0007 a0001c0004t0001g0014 a0001c0004t0001g0015 others(47): Show |
53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1546+1539A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310891 | |||||||
chr5:180310927 | C | T | 30 | a0001c0001t0001g0284 a0001c0001t0009g0290 a0001c0005t0001g0219 others(27): Show |
30 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1546+1503G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310927 | |||||||
chr5:180310977 | G | T | 5 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0005g0366 others(2): Show |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+1453C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180310977 | |||||||
chr5:180311025 | T | G | 1 | a0003c0006t0001g0245 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1546+1405A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311025 | |||||||
chr5:180311085 | T | C | 5 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0005g0366 others(2): Show |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+1345A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311085 | |||||||
chr5:180311087 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(23): Show |
31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1546+1343C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311087 | |||||||
chr5:180311101 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(239): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1546+1329T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311101 | |||||||
chr5:180311149 | G | A | 5 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0005g0366 others(2): Show |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+1281C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311149 | |||||||
chr5:180311162 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(181): Show |
200 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.1546+1268A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311162 | |||||||
chr5:180311213 | C | T | 84 | a0001c0005t0002g0082 a0001c0005t0002g0107 a0002c0002t0002g0003 others(81): Show |
92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1546+1217G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311213 | |||||||
chr5:180311237 | T | C | 50 | a0001c0004t0001g0007 a0001c0004t0001g0014 a0001c0004t0001g0015 others(47): Show |
53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1546+1193A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311237 | |||||||
chr5:180311257 | C | T | 1 | a0002c0002t0002g0280 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1546+1173G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311257 | |||||||
chr5:180311278 | A | G | 3 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 |
3 | HG02145.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1546+1152T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311278 | |||||||
chr5:180311437 | T | G | 30 | a0001c0001t0001g0284 a0001c0001t0009g0290 a0001c0005t0001g0219 others(27): Show |
30 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1546+993A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311437 | |||||||
chr5:180311440 | T | C | 1 | a0001c0005t0005g0371 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1546+990A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311440 | |||||||
chr5:180311517 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(178): Show |
198 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.1546+913A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311517 | |||||||
chr5:180311638 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(110): Show |
126 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1546+792T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311638 | |||||||
chr5:180311713 | C | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(129): Show |
145 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1546+717G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311713 | |||||||
chr5:180311715 | G | A | 3 | a0001c0004t0020g0359 a0005c0010t0001g0132 a0005c0010t0001g0133 |
3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1546+715C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311715 | |||||||
chr5:180311717 | GA | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(129): Show |
145 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1546+712delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311717 | |||||||
chr5:180311727 | T | A | 1 | a0002c0002t0002g0216 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1546+703A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311727 | |||||||
chr5:180311743 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(127): Show |
143 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1546+687C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311743 | |||||||
chr5:180311782 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(127): Show |
143 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1546+648C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311782 | |||||||
chr5:180311796 | G | A | 1 | a0001c0003t0001g0303 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1546+634C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311796 | |||||||
chr5:180311800 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(129): Show |
145 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1546+630T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311800 | |||||||
chr5:180311925 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(127): Show |
142 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1546+505C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311925 | |||||||
chr5:180311984 | AGGCAGGG others(17): Show |
A | 87 | a0001c0004t0020g0359 a0001c0005t0002g0082 a0001c0005t0002g0107 others(84): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1546+422_1546+445d others(26): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311984 | |||||||
chr5:180311988 | AGGGAGGT others(33): Show |
A | 76 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(73): Show |
81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1546+402_1546+441d others(42): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180311988 | |||||||
chr5:180312008 | G | GACCAGGG others(1): Show |
44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(41): Show |
49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+421_1546+422i others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312008 | |||||||
chr5:180312009 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+421C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312009 | |||||||
chr5:180312010 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+420C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312010 | |||||||
chr5:180312030 | G | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(22): Show |
30 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1546+400C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312030 | |||||||
chr5:180312034 | G | T | 87 | a0001c0004t0020g0359 a0001c0005t0002g0082 a0001c0005t0002g0107 others(84): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1546+396C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312034 | |||||||
chr5:180312035 | T | C | 49 | a0001c0004t0001g0005 a0001c0004t0001g0007 a0001c0004t0001g0014 others(46): Show |
53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1546+395A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312035 | |||||||
chr5:180312036 | G | GAGGACCA others(8): Show |
1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+393_1546+394i others(17): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312036 | |||||||
chr5:180312049 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+381C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312049 | |||||||
chr5:180312050 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(41): Show |
49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+380C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312050 | |||||||
chr5:180312050 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+380C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312050 | |||||||
chr5:180312050 | GCAGGGAG others(49): Show |
G | 3 | a0001c0004t0001g0134 a0001c0004t0001g0270 a0001c0017t0001g0232 |
3 | HG02647.hp1 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1546+324_1546+379d others(58): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312050 | |||||||
chr5:180312058 | G | GCAGGGAG others(49): Show |
1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1546+371_1546+372i others(58): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312058 | |||||||
chr5:180312066 | GCGGGGAG others(33): Show |
G | 87 | a0001c0004t0020g0359 a0001c0005t0002g0082 a0001c0005t0002g0107 others(84): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1546+324_1546+363d others(42): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312066 | |||||||
chr5:180312068 | G | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(41): Show |
49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+362C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312068 | |||||||
chr5:180312068 | GGGGAGGC others(17): Show |
G | 49 | a0001c0004t0001g0005 a0001c0004t0001g0007 a0001c0004t0001g0014 others(46): Show |
53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1546+338_1546+361d others(26): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312068 | |||||||
chr5:180312074 | GCTGAGGA others(1): Show |
G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(41): Show |
49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+348_1546+355d others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312074 | |||||||
chr5:180312084 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(41): Show |
49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+346T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312084 | |||||||
chr5:180312091 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(41): Show |
49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+339G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312091 | |||||||
chr5:180312092 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(41): Show |
49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+338T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312092 | |||||||
chr5:180312114 | G | GCAGGGAG others(9): Show |
1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1546+315_1546+316i others(18): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312114 | |||||||
chr5:180312116 | A | G | 88 | a0001c0001t0001g0194 a0001c0004t0020g0359 a0001c0005t0002g0082 others(85): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1546+314T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312116 | |||||||
chr5:180312121 | G | A | 87 | a0001c0004t0020g0359 a0001c0005t0002g0082 a0001c0005t0002g0107 others(84): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1546+309C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312121 | |||||||
chr5:180312123 | C | CAGGGAGG others(9): Show |
1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+306_1546+307i others(18): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312123 | |||||||
chr5:180312123 | C | T | 88 | a0001c0003t0001g0120 a0001c0004t0020g0359 a0001c0005t0002g0082 others(85): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1546+307G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312123 | |||||||
chr5:180312124 | GGGGAGGC others(17): Show |
G | 4 | a0001c0003t0001g0120 a0001c0009t0001g0180 a0001c0009t0001g0356 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546+282_1546+305d others(26): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312124 | |||||||
chr5:180312124 | GGGGAGGC others(73): Show |
G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(41): Show |
49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+226_1546+305d others(82): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312124 | |||||||
chr5:180312137 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+293T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312137 | |||||||
chr5:180312138 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+292G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312138 | |||||||
chr5:180312156 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+274A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312156 | |||||||
chr5:180312158 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+272T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312158 | |||||||
chr5:180312160 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+270C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312160 | |||||||
chr5:180312161 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+269T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312161 | |||||||
chr5:180312162 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+268G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312162 | |||||||
chr5:180312164 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+266T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312164 | |||||||
chr5:180312164 | AGGGAGGC others(25): Show |
A | 72 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(69): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1546+234_1546+265d others(34): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312164 | |||||||
chr5:180312171 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+259G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312171 | |||||||
chr5:180312172 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+258T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312172 | |||||||
chr5:180312172 | AGGGAGGC others(17): Show |
A | 84 | a0001c0005t0002g0082 a0001c0005t0002g0107 a0002c0002t0002g0003 others(81): Show |
92 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.1546+234_1546+257d others(26): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312172 | |||||||
chr5:180312186 | C | CCAGGGAG others(425): Show |
1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1546+243_1546+244i others(434): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312186 | |||||||
chr5:180312196 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1546+234C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312196 | |||||||
chr5:180312196 | G | GGGGAGGC others(1): Show |
49 | a0001c0004t0001g0005 a0001c0004t0001g0007 a0001c0004t0001g0014 others(46): Show |
53 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1546+226_1546+233d others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312196 | |||||||
chr5:180312196 | GGGGAGGC others(1): Show |
G | 10 | a0001c0001t0001g0264 a0001c0001t0001g0323 a0001c0001t0001g0328 others(7): Show |
10 | HG01099.hp2 HG01934.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546+226_1546+233d others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312196 | |||||||
chr5:180312204 | A | G | 162 | a0001c0001t0001g0194 a0001c0003t0001g0002 a0001c0003t0001g0018 others(159): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1546+226T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312204 | |||||||
chr5:180312231 | G | C | 1 | a0001c0004t0001g0037 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1546+199C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312231 | |||||||
chr5:180312241 | A | AG | 10 | a0002c0002t0002g0071 a0002c0002t0002g0086 a0002c0002t0002g0109 others(7): Show |
10 | HG00597.hp1 HG01175.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.1546+188dupC | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312241 | |||||||
chr5:180312244 | G | T | 1 | a0001c0005t0002g0082 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1546+186C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312244 | |||||||
chr5:180312247 | A | G | 83 | a0001c0005t0002g0082 a0001c0005t0002g0107 a0002c0002t0002g0003 others(80): Show |
91 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1546+183T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312247 | |||||||
chr5:180312247 | A | T | 1 | a0002c0002t0002g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1546+183T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312247 | |||||||
chr5:180312256 | C | T | 3 | a0001c0004t0020g0359 a0005c0010t0001g0132 a0005c0010t0001g0133 |
3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1546+174G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 15/18 | chr5 | 180312256 | |||||||
chr5:180312557 | A | G | 1 | a0001c0003t0001g0030 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1432-13T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312557 | |||||||
chr5:180312826 | G | C | 1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1432-282C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312826 | |||||||
chr5:180312836 | G | A | 3 | a0001c0004t0020g0359 a0005c0010t0001g0132 a0005c0010t0001g0133 |
3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1432-292C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312836 | |||||||
chr5:180312839 | C | T | 1 | a0002c0002t0002g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1432-295G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312839 | |||||||
chr5:180312858 | C | A | 1 | a0001c0001t0005g0370 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1432-314G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312858 | |||||||
chr5:180312867 | A | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(110): Show |
126 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1432-323T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312867 | |||||||
chr5:180312925 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(26): Show |
34 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1432-381G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312925 | |||||||
chr5:180312926 | G | A | 3 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 |
3 | HG02145.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1432-382C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312926 | |||||||
chr5:180312942 | A | G | 4 | a0002c0002t0002g0047 a0002c0002t0002g0048 a0002c0002t0002g0316 others(1): Show |
4 | HG00558.hp1 NA18945.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1432-398T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312942 | |||||||
chr5:180312951 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(110): Show |
126 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1432-407C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312951 | |||||||
chr5:180312958 | G | A | 19 | a0001c0005t0004g0045 a0001c0005t0004g0058 a0001c0005t0004g0130 others(16): Show |
19 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1432-414C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312958 | |||||||
chr5:180312959 | T | G | 1 | a0003c0013t0001g0240 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1432-415A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312959 | |||||||
chr5:180312989 | A | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(115): Show |
131 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1432-445T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180312989 | |||||||
chr5:180313020 | C | A | 1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1432-476G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313020 | |||||||
chr5:180313020 | C | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(285): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1432-476G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313020 | |||||||
chr5:180313023 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(139): Show |
155 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1432-479A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313023 | |||||||
chr5:180313046 | G | A | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1432-502C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313046 | |||||||
chr5:180313066 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(26): Show |
34 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1432-522G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313066 | |||||||
chr5:180313073 | G | T | 1 | a0002c0008t0001g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1432-529C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313073 | |||||||
chr5:180313074 | G | C | 5 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0005g0366 others(2): Show |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1432-530C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313074 | |||||||
chr5:180313080 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(115): Show |
131 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1432-536C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313080 | |||||||
chr5:180313098 | C | T | 9 | a0001c0005t0003g0206 a0001c0005t0003g0207 a0001c0005t0003g0209 others(6): Show |
9 | HG01167.hp2 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1432-554G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313098 | |||||||
chr5:180313100 | G | A | 1 | a0001c0005t0021g0368 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1432-556C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313100 | |||||||
chr5:180313100 | G | C | 2 | a0001c0004t0001g0007 a0001c0004t0001g0186 |
3 | NA18969.hp1 NA18981.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1432-556C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313100 | |||||||
chr5:180313108 | C | T | 90 | a0001c0003t0001g0221 a0001c0005t0001g0219 a0001c0005t0002g0082 others(87): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.1432-564G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313108 | |||||||
chr5:180313146 | C | T | 6 | a0003c0006t0001g0235 a0003c0006t0001g0236 a0003c0006t0001g0237 others(3): Show |
6 | NA18946.hp1 NA18966.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1432-602G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313146 | |||||||
chr5:180313223 | C | T | 1 | a0001c0004t0001g0352 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1431+584G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313223 | |||||||
chr5:180313239 | G | A | 91 | a0001c0005t0001g0219 a0001c0005t0002g0082 a0001c0005t0002g0107 others(88): Show |
99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1431+568C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313239 | |||||||
chr5:180313337 | A | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(23): Show |
31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1431+470T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313337 | |||||||
chr5:180313366 | C | T | 91 | a0001c0005t0001g0219 a0001c0005t0002g0082 a0001c0005t0002g0107 others(88): Show |
99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1431+441G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313366 | |||||||
chr5:180313382 | G | C | 4 | a0002c0002t0002g0047 a0002c0002t0002g0048 a0002c0002t0002g0316 others(1): Show |
4 | HG00558.hp1 NA18945.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1431+425C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313382 | |||||||
chr5:180313392 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG00544.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1431+415G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313392 | |||||||
chr5:180313398 | C | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(307): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.1431+409G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313398 | |||||||
chr5:180313401 | C | T | 1 | a0001c0003t0001g0287 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1431+406G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313401 | |||||||
chr5:180313402 | T | C | 1 | a0001c0003t0001g0347 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1431+405A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313402 | |||||||
chr5:180313416 | C | T | 1 | a0001c0003t0001g0287 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1431+391G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313416 | |||||||
chr5:180313420 | T | C | 162 | a0001c0004t0001g0007 a0001c0004t0001g0037 a0001c0004t0001g0041 others(159): Show |
172 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.1431+387A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313420 | |||||||
chr5:180313451 | T | C | 77 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(74): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1431+356A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313451 | |||||||
chr5:180313453 | T | C | 75 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(72): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1431+354A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313453 | |||||||
chr5:180313455 | G | GT | 77 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(74): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1431+351_1431+352i others(3): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313455 | |||||||
chr5:180313459 | G | A | 3 | a0001c0001t0001g0264 a0001c0001t0001g0323 a0001c0001t0001g0328 |
3 | HG01099.hp2 HG01934.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1431+348C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313459 | |||||||
chr5:180313462 | T | C | 235 | a0001c0001t0001g0196 a0001c0001t0001g0284 a0001c0001t0009g0290 others(232): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.1431+345A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313462 | |||||||
chr5:180313469 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(187): Show |
208 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1431+338T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313469 | |||||||
chr5:180313478 | T | G | 1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1431+329A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313478 | |||||||
chr5:180313507 | G | T | 1 | a0001c0001t0001g0328 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1431+300C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313507 | |||||||
chr5:180313526 | C | G | 5 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0005g0366 others(2): Show |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1431+281G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313526 | |||||||
chr5:180313527 | T | C | 2 | a0001c0004t0001g0217 a0001c0004t0001g0218 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1431+280A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313527 | |||||||
chr5:180313527 | T | G | 88 | a0001c0005t0002g0082 a0001c0005t0002g0107 a0001c0005t0003g0033 others(85): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.1431+280A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313527 | |||||||
chr5:180313539 | G | A | 27 | a0001c0001t0009g0290 a0001c0004t0001g0134 a0001c0004t0001g0270 others(24): Show |
27 | HG01167.hp2 HG02055.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1431+268C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313539 | |||||||
chr5:180313546 | C | T | 1 | a0001c0005t0019g0361 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1431+261G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313546 | |||||||
chr5:180313550 | C | A | 4 | a0002c0002t0002g0038 a0002c0002t0002g0039 a0002c0002t0002g0110 others(1): Show |
4 | HG01943.hp1 HG03130.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1431+257G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313550 | |||||||
chr5:180313552 | T | A | 4 | a0002c0002t0002g0038 a0002c0002t0002g0039 a0002c0002t0002g0110 others(1): Show |
4 | HG01943.hp1 HG03130.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1431+255A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313552 | |||||||
chr5:180313563 | C | G | 118 | a0001c0001t0001g0284 a0001c0001t0009g0290 a0001c0003t0001g0002 others(115): Show |
123 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1431+244G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313563 | |||||||
chr5:180313576 | T | C | 55 | a0001c0001t0001g0100 a0001c0001t0001g0196 a0001c0004t0001g0005 others(52): Show |
59 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1431+231A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313576 | |||||||
chr5:180313606 | T | TAAAATA | 91 | a0001c0004t0001g0061 a0001c0005t0001g0219 a0001c0005t0002g0082 others(88): Show |
99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1431+195_1431+200d others(8): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313606 | |||||||
chr5:180313626 | A | T | 3 | a0001c0001t0001g0115 a0001c0001t0005g0363 a0001c0001t0005g0364 |
3 | HG03491.hp1 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1431+181T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313626 | |||||||
chr5:180313640 | C | T | 167 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(164): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1431+167G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313640 | |||||||
chr5:180313646 | T | G | 4 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1431+161A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313646 | |||||||
chr5:180313705 | G | A | 20 | a0001c0001t0005g0365 a0001c0001t0005g0367 a0001c0004t0001g0134 others(17): Show |
20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1431+102C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 14/18 | chr5 | 180313705 | |||||||
chr5:180314131 | T | C | 2 | a0002c0002t0002g0086 a0002c0002t0002g0129 |
2 | HG01175.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1274-167A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314131 | |||||||
chr5:180314327 | G | C | 1 | a0001c0004t0005g0366 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1274-363C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314327 | |||||||
chr5:180314374 | C | A | 165 | a0001c0001t0001g0111 a0001c0003t0001g0002 a0001c0003t0001g0018 others(162): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1274-410G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314374 | |||||||
chr5:180314411 | A | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(266): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.1274-447T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314411 | |||||||
chr5:180314446 | A | G | 5 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0005g0366 others(2): Show |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1274-482T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314446 | |||||||
chr5:180314448 | T | C | 76 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(73): Show |
81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1274-484A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314448 | |||||||
chr5:180314534 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(99): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.1274-570T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314534 | |||||||
chr5:180314564 | A | G | 3 | a0001c0003t0001g0092 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG00280.hp2 HG00323.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1274-600T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314564 | |||||||
chr5:180314633 | C | T | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1274-669G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314633 | |||||||
chr5:180314659 | A | T | 3 | a0001c0004t0001g0049 a0001c0004t0001g0050 a0001c0004t0001g0056 |
3 | HG01934.hp2 HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1274-695T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314659 | |||||||
chr5:180314765 | C | T | 5 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0005g0366 others(2): Show |
5 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1274-801G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314765 | |||||||
chr5:180314879 | T | G | 2 | a0001c0004t0001g0344 a0001c0005t0001g0219 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1274-915A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314879 | |||||||
chr5:180314894 | C | T | 25 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(22): Show |
25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1274-930G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314894 | |||||||
chr5:180314899 | C | T | 1 | a0002c0002t0002g0110 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1274-935G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314899 | |||||||
chr5:180314981 | C | T | 89 | a0001c0004t0001g0005 a0001c0004t0001g0007 a0001c0004t0001g0014 others(86): Show |
94 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1274-1017G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180314981 | |||||||
chr5:180315022 | C | T | 25 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(22): Show |
25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1274-1058G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315022 | |||||||
chr5:180315030 | C | A | 1 | a0001c0001t0001g0317 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1274-1066G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315030 | |||||||
chr5:180315161 | G | A | 20 | a0001c0001t0005g0369 a0001c0005t0004g0045 a0001c0005t0004g0058 others(17): Show |
20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1273+1180C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315161 | |||||||
chr5:180315169 | G | GTTTTTC | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273+1166_1273+117 others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315169 | |||||||
chr5:180315181 | C | CT | 9 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(6): Show |
9 | HG02145.hp2 HG02148.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1273+1159dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315181 | |||||||
chr5:180315181 | C | CTTTTCT | 19 | a0001c0005t0004g0045 a0001c0005t0004g0058 a0001c0005t0004g0130 others(16): Show |
19 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1273+1159_1273+116 others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315181 | |||||||
chr5:180315201 | G | A | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+1140C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315201 | |||||||
chr5:180315204 | G | A | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+1137C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315204 | |||||||
chr5:180315208 | C | T | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1273+1133G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315208 | |||||||
chr5:180315227 | G | T | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+1114C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315227 | |||||||
chr5:180315233 | A | T | 4 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1273+1108T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315233 | |||||||
chr5:180315240 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(152): Show |
170 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1273+1101G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315240 | |||||||
chr5:180315252 | A | G | 20 | a0001c0001t0009g0290 a0001c0005t0003g0089 a0001c0005t0003g0102 others(17): Show |
20 | HG01167.hp2 HG02071.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1273+1089T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315252 | |||||||
chr5:180315262 | C | G | 24 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(21): Show |
24 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1273+1079G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315262 | |||||||
chr5:180315263 | C | T | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+1078G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315263 | |||||||
chr5:180315279 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(274): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.1273+1062C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315279 | |||||||
chr5:180315329 | C | T | 25 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(22): Show |
25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1273+1012G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315329 | |||||||
chr5:180315334 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1273+1007G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315334 | |||||||
chr5:180315347 | G | T | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+994C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315347 | |||||||
chr5:180315379 | T | C | 1 | a0001c0001t0005g0377 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1273+962A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315379 | |||||||
chr5:180315384 | G | T | 1 | a0001c0001t0005g0377 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1273+957C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315384 | |||||||
chr5:180315389 | A | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0208 |
3 | HG01884.hp2 HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1273+952T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315389 | |||||||
chr5:180315414 | G | A | 24 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(21): Show |
24 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1273+927C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315414 | |||||||
chr5:180315425 | A | G | 1 | a0001c0021t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1273+916T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315425 | |||||||
chr5:180315430 | A | G | 1 | a0001c0021t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1273+911T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315430 | |||||||
chr5:180315460 | G | A | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+881C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315460 | |||||||
chr5:180315468 | G | A | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+873C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315468 | |||||||
chr5:180315469 | C | T | 1 | a0001c0005t0005g0371 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1273+872G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315469 | |||||||
chr5:180315474 | G | A | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273+867C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315474 | |||||||
chr5:180315530 | T | C | 13 | a0001c0001t0001g0019 a0001c0001t0001g0115 a0001c0001t0001g0123 others(10): Show |
15 | HG00280.hp1 HG02818.hp1 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.1273+811A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315530 | |||||||
chr5:180315609 | G | A | 20 | a0001c0001t0009g0290 a0001c0005t0003g0089 a0001c0005t0003g0102 others(17): Show |
20 | HG01167.hp2 HG02071.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.1273+732C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315609 | |||||||
chr5:180315628 | A | G | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+713T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315628 | |||||||
chr5:180315723 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1273+618C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315723 | |||||||
chr5:180315934 | A | G | 1 | a0001c0004t0001g0049 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1273+407T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315934 | |||||||
chr5:180315988 | T | C | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+353A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315988 | |||||||
chr5:180315990 | C | T | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+351G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180315990 | |||||||
chr5:180316032 | C | T | 39 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(36): Show |
40 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1273+309G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316032 | |||||||
chr5:180316084 | G | A | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+257C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316084 | |||||||
chr5:180316087 | A | G | 48 | a0001c0004t0001g0005 a0001c0004t0001g0007 a0001c0004t0001g0014 others(45): Show |
52 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1273+254T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316087 | |||||||
chr5:180316101 | C | A | 41 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(38): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1273+240G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316101 | |||||||
chr5:180316174 | C | T | 25 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(22): Show |
25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1273+167G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316174 | |||||||
chr5:180316205 | C | A | 1 | a0001c0005t0003g0283 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1273+136G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316205 | |||||||
chr5:180316218 | C | T | 14 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(11): Show |
15 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(12): Show |
intron_variant | MODIFIER | c.1273+123G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316218 | |||||||
chr5:180316260 | G | T | 16 | a0001c0018t0006g0308 a0003c0006t0001g0017 a0003c0006t0001g0043 others(13): Show |
17 | HG00099.hp1 HG01975.hp1 HG03239.hp1 others(14): Show |
intron_variant | MODIFIER | c.1273+81C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316260 | |||||||
chr5:180316272 | T | A | 25 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(22): Show |
25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.1273+69A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316272 | |||||||
chr5:180316294 | C | T | 1 | a0001c0005t0019g0361 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1273+47G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316294 | |||||||
chr5:180316308 | T | C | 3 | a0001c0004t0020g0359 a0005c0010t0001g0132 a0005c0010t0001g0133 |
3 | HG02965.hp1 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1273+33A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 13/18 | chr5 | 180316308 | |||||||
chr5:180316541 | C | A | 1 | a0001c0004t0001g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1153-80G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316541 | |||||||
chr5:180316553 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(23): Show |
31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1153-92G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316553 | |||||||
chr5:180316569 | A | G | 1 | a0002c0007t0001g0320 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1153-108T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316569 | |||||||
chr5:180316637 | C | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(23): Show |
31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1152+127G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316637 | |||||||
chr5:180316730 | C | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(17): Show |
25 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1152+34G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316730 | |||||||
chr5:180316731 | G | A | 87 | a0001c0001t0001g0111 a0001c0004t0001g0188 a0001c0005t0002g0082 others(84): Show |
95 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1152+33C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316731 | |||||||
chr5:180316733 | C | T | 1 | a0001c0003t0001g0201 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1152+31G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 12/18 | chr5 | 180316733 | |||||||
chr5:180316948 | G | A | 7 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0001g0344 others(4): Show |
7 | HG02451.hp1 HG02976.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1054+15C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 11/18 | chr5 | 180316948 | |||||||
chr5:180317270 | A | G | 1 | a0001c0004t0001g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.959-212T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317270 | |||||||
chr5:180317364 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.959-306G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317364 | |||||||
chr5:180317384 | C | G | 4 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-326G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317384 | |||||||
chr5:180317455 | T | C | 70 | a0001c0003t0001g0002 a0001c0003t0001g0018 a0001c0003t0001g0020 others(67): Show |
75 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.959-397A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317455 | |||||||
chr5:180317459 | C | T | 2 | a0001c0003t0001g0275 a0001c0003t0001g0297 |
2 | NA19084.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.959-401G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317459 | |||||||
chr5:180317464 | TAAAAACC others(301): Show |
T | 4 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-714_959-407del | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317464 | |||||||
chr5:180317488 | A | G | 85 | a0001c0001t0001g0111 a0001c0004t0001g0188 a0001c0005t0002g0082 others(82): Show |
92 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.959-430T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317488 | |||||||
chr5:180317503 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0325 |
2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.959-445A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317503 | |||||||
chr5:180317509 | CAGCACTT others(5): Show |
C | 1 | a0002c0002t0002g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.959-463_959-452del others(12): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317509 | |||||||
chr5:180317525 | C | T | 8 | a0001c0004t0001g0037 a0001c0004t0001g0042 a0001c0004t0001g0054 others(5): Show |
8 | HG00639.hp1 HG01106.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.959-467G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317525 | |||||||
chr5:180317529 | G | A | 6 | a0001c0004t0001g0037 a0001c0004t0001g0042 a0001c0004t0001g0054 others(3): Show |
6 | HG00639.hp1 HG01106.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.959-471C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317529 | |||||||
chr5:180317531 | G | A | 1 | a0001c0003t0001g0105 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.959-473C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317531 | |||||||
chr5:180317534 | C | T | 1 | a0001c0003t0001g0253 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.959-476G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317534 | |||||||
chr5:180317535 | G | A | 2 | a0001c0004t0001g0134 a0001c0004t0001g0270 |
2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.959-477C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317535 | |||||||
chr5:180317544 | A | G | 5 | a0001c0001t0005g0377 a0001c0003t0001g0253 a0001c0004t0001g0217 others(2): Show |
5 | HG02630.hp1 HG02735.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.959-486T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317544 | |||||||
chr5:180317555 | C | G | 2 | a0002c0002t0002g0006 a0002c0002t0002g0009 |
2 | NA18940.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.959-497G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317555 | |||||||
chr5:180317555 | C | T | 5 | a0001c0005t0003g0033 a0001c0005t0003g0088 a0001c0005t0003g0265 others(2): Show |
5 | HG02717.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.959-497G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317555 | |||||||
chr5:180317566 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0005g0377 a0001c0003t0001g0002 others(77): Show |
86 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.959-508G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317566 | |||||||
chr5:180317573 | A | C | 7 | a0001c0001t0005g0377 a0001c0003t0001g0031 a0001c0003t0001g0230 others(4): Show |
7 | HG01192.hp2 HG02886.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.959-515T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317573 | |||||||
chr5:180317576 | A | G | 8 | a0001c0001t0005g0370 a0001c0001t0005g0377 a0001c0003t0001g0031 others(5): Show |
8 | HG01192.hp2 HG02257.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.959-518T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317576 | |||||||
chr5:180317586 | C | T | 4 | a0002c0002t0002g0038 a0002c0002t0002g0039 a0002c0002t0002g0110 others(1): Show |
4 | HG01943.hp1 HG03130.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.959-528G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317586 | |||||||
chr5:180317639 | G | C | 1 | a0001c0004t0001g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.959-581C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317639 | |||||||
chr5:180317650 | T | G | 1 | a0001c0005t0007g0304 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.959-592A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317650 | |||||||
chr5:180317708 | G | A | 2 | a0001c0004t0001g0083 a0001c0004t0001g0121 |
2 | HG02486.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.959-650C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317708 | |||||||
chr5:180317714 | G | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(309): Show |
335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.959-656C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317714 | |||||||
chr5:180317721 | A | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(309): Show |
335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.959-663T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317721 | |||||||
chr5:180317723 | C | T | 6 | a0001c0003t0001g0002 a0001c0003t0001g0252 a0001c0003t0001g0279 others(3): Show |
9 | HG01070.hp2 HG01175.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.959-665G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317723 | |||||||
chr5:180317746 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(185): Show |
203 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.959-688T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317746 | |||||||
chr5:180317758 | C | CA | 8 | a0001c0001t0001g0019 a0001c0001t0001g0115 a0001c0001t0001g0176 others(5): Show |
8 | HG01106.hp2 HG02738.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.959-701dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317758 | |||||||
chr5:180317758 | CA | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(272): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.959-701delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317758 | |||||||
chr5:180317889 | G | C | 1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.959-831C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317889 | |||||||
chr5:180317901 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.959-843G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317901 | |||||||
chr5:180317927 | C | T | 1 | a0002c0002t0002g0166 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.958+866G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317927 | |||||||
chr5:180317941 | A | G | 4 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+852T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317941 | |||||||
chr5:180317970 | T | G | 4 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+823A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180317970 | |||||||
chr5:180318027 | T | C | 4 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+766A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318027 | |||||||
chr5:180318168 | C | A | 4 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.958+625G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318168 | |||||||
chr5:180318184 | T | C | 2 | a0003c0014t0001g0292 a0003c0014t0001g0302 |
2 | NA18946.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.958+609A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318184 | |||||||
chr5:180318312 | C | T | 1 | a0001c0005t0005g0371 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.958+481G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318312 | |||||||
chr5:180318347 | C | A | 27 | a0001c0004t0001g0134 a0001c0004t0001g0270 a0001c0005t0004g0045 others(24): Show |
27 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.958+446G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318347 | |||||||
chr5:180318385 | G | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(23): Show |
31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.958+408C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318385 | |||||||
chr5:180318389 | C | T | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.958+404G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318389 | |||||||
chr5:180318413 | C | G | 85 | a0001c0001t0001g0111 a0001c0004t0001g0188 a0001c0005t0002g0082 others(82): Show |
92 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.958+380G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318413 | |||||||
chr5:180318437 | C | A | 2 | a0001c0004t0001g0062 a0001c0004t0001g0256 |
2 | HG00642.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.958+356G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318437 | |||||||
chr5:180318461 | C | T | 1 | a0002c0008t0001g0182 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.958+332G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318461 | |||||||
chr5:180318515 | G | A | 1 | a0001c0005t0004g0164 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.958+278C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318515 | |||||||
chr5:180318534 | GCAGCTGA others(2): Show |
G | 5 | a0001c0005t0005g0371 a0001c0009t0001g0180 a0001c0009t0001g0356 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.958+250_958+258del others(9): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318534 | |||||||
chr5:180318549 | G | C | 1 | a0001c0004t0001g0352 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.958+244C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318549 | |||||||
chr5:180318607 | A | G | 68 | a0001c0001t0001g0111 a0001c0004t0001g0188 a0002c0002t0001g0097 others(65): Show |
74 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.958+186T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318607 | |||||||
chr5:180318666 | C | T | 7 | a0001c0004t0001g0195 a0001c0004t0001g0204 a0001c0004t0005g0373 others(4): Show |
7 | HG02451.hp1 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.958+127G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318666 | |||||||
chr5:180318721 | C | CAG | 44 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(41): Show |
49 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.958+70_958+71dupCT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318721 | |||||||
chr5:180318760 | G | A | 3 | a0001c0003t0001g0092 a0001c0003t0001g0093 a0001c0003t0001g0094 |
3 | HG00280.hp2 HG00323.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.958+33C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 10/18 | chr5 | 180318760 | |||||||
chr5:180318963 | C | T | 1 | a0002c0002t0002g0095 | 1 | NA18962.hp2 | splice_region_variant&intron_variant | LOW | c.795-7G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180318963 | |||||||
chr5:180319098 | G | A | 1 | a0001c0004t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.795-142C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319098 | |||||||
chr5:180319191 | A | C | 4 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.795-235T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319191 | |||||||
chr5:180319231 | TATA | T | 25 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(22): Show |
25 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.795-278_795-276del others(3): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319231 | |||||||
chr5:180319309 | A | G | 5 | a0001c0005t0002g0107 a0002c0002t0002g0098 a0002c0002t0002g0108 others(2): Show |
6 | HG01074.hp1 HG01261.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-353T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319309 | |||||||
chr5:180319391 | C | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(23): Show |
31 | HG01255.hp1 HG01258.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.795-435G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319391 | |||||||
chr5:180319551 | C | G | 1 | a0001c0001t0009g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.795-595G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319551 | |||||||
chr5:180319708 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.795-752C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319708 | |||||||
chr5:180319817 | A | T | 23 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(20): Show |
23 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.795-861T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319817 | |||||||
chr5:180319852 | T | G | 26 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(23): Show |
26 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.795-896A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180319852 | |||||||
chr5:180320032 | G | A | 1 | a0001c0005t0011g0379 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.795-1076C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320032 | |||||||
chr5:180320100 | C | A | 28 | a0001c0001t0001g0284 a0001c0001t0009g0290 a0001c0005t0003g0033 others(25): Show |
28 | HG01167.hp2 HG02071.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.795-1144G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320100 | |||||||
chr5:180320118 | G | A | 1 | a0001c0003t0001g0200 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.795-1162C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320118 | |||||||
chr5:180320149 | T | C | 1 | a0001c0003t0014g0336 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.795-1193A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320149 | |||||||
chr5:180320149 | T | G | 2 | a0001c0004t0001g0344 a0001c0005t0001g0219 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.795-1193A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320149 | |||||||
chr5:180320154 | G | A | 1 | a0001c0004t0001g0197 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.795-1198C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320154 | |||||||
chr5:180320194 | G | A | 1 | a0001c0004t0008g0029 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.795-1238C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320194 | |||||||
chr5:180320235 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.795-1279C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320235 | |||||||
chr5:180320270 | G | A | 2 | a0001c0001t0001g0284 a0001c0005t0019g0361 |
2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.795-1314C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320270 | |||||||
chr5:180320282 | G | A | 2 | a0001c0004t0001g0344 a0001c0005t0001g0219 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.795-1326C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320282 | |||||||
chr5:180320291 | C | A | 2 | a0001c0001t0005g0365 a0001c0001t0005g0367 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.795-1335G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320291 | |||||||
chr5:180320363 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.795-1407G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320363 | |||||||
chr5:180320491 | G | A | 24 | a0001c0004t0001g0134 a0001c0004t0001g0217 a0001c0004t0001g0218 others(21): Show |
24 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.795-1535C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320491 | |||||||
chr5:180320495 | G | T | 40 | a0001c0004t0001g0007 a0001c0004t0001g0014 a0001c0004t0001g0015 others(37): Show |
43 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.795-1539C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320495 | |||||||
chr5:180320511 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(315): Show |
341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.795-1555T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320511 | |||||||
chr5:180320539 | A | G | 292 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(289): Show |
315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.795-1583T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320539 | |||||||
chr5:180320543 | C | T | 1 | a0001c0001t0009g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.795-1587G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320543 | |||||||
chr5:180320564 | G | C | 1 | a0001c0005t0004g0149 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.795-1608C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320564 | |||||||
chr5:180320601 | C | T | 1 | a0001c0004t0001g0225 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.795-1645G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320601 | |||||||
chr5:180320809 | G | C | 50 | a0001c0001t0001g0233 a0001c0004t0001g0005 a0001c0004t0001g0007 others(47): Show |
54 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.795-1853C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320809 | |||||||
chr5:180320888 | G | A | 5 | a0001c0004t0001g0015 a0001c0004t0001g0179 a0001c0004t0001g0257 others(2): Show |
6 | HG02074.hp1 HG02083.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-1932C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320888 | |||||||
chr5:180320949 | A | G | 1 | a0005c0010t0001g0133 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.795-1993T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320949 | |||||||
chr5:180320967 | A | ACTTTGTA others(27): Show |
1 | a0006c0016t0002g0044 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.795-2012_795-2011i others(36): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320967 | |||||||
chr5:180320982 | A | ATACAAAT others(26): Show |
1 | a0001c0005t0007g0353 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.795-2027_795-2026i others(35): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320982 | |||||||
chr5:180320982 | A | ATACAAAT others(26): Show |
250 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0111 others(247): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.795-2059_795-2027d others(35): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320982 | |||||||
chr5:180320982 | A | ATACAAAT others(59): Show |
8 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0196 others(5): Show |
8 | HG02602.hp1 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.795-2092_795-2027d others(68): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320982 | |||||||
chr5:180320982 | A | G | 1 | a0006c0016t0002g0044 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.795-2026T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180320982 | |||||||
chr5:180321015 | G | GTACAAAT others(59): Show |
8 | a0001c0003t0001g0198 a0001c0004t0001g0195 a0001c0004t0005g0373 others(5): Show |
8 | HG02145.hp2 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.795-2060_795-2059i others(68): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321015 | |||||||
chr5:180321127 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0208 a0001c0005t0003g0210 others(2): Show |
6 | HG01884.hp2 HG02055.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.795-2171A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321127 | |||||||
chr5:180321183 | A | AT | 12 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0124 others(9): Show |
13 | HG01884.hp2 HG02055.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.795-2228dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321183 | |||||||
chr5:180321207 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0099 others(131): Show |
146 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.795-2251G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321207 | |||||||
chr5:180321300 | G | A | 1 | a0001c0004t0003g0183 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.795-2344C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321300 | |||||||
chr5:180321430 | G | C | 20 | a0001c0001t0001g0158 a0001c0005t0004g0045 a0001c0005t0004g0058 others(17): Show |
20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.795-2474C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321430 | |||||||
chr5:180321454 | T | C | 76 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0122 others(73): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.795-2498A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321454 | |||||||
chr5:180321591 | C | T | 1 | a0001c0004t0001g0171 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.794+2597G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321591 | |||||||
chr5:180321611 | G | A | 1 | a0001c0004t0001g0037 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.794+2577C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321611 | |||||||
chr5:180321631 | T | C | 93 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0111 others(90): Show |
100 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.794+2557A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321631 | |||||||
chr5:180321690 | A | G | 278 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0035 others(275): Show |
297 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.794+2498T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321690 | |||||||
chr5:180321758 | G | A | 2 | a0001c0005t0003g0125 a0001c0005t0003g0185 |
2 | HG02723.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.794+2430C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321758 | |||||||
chr5:180321761 | G | GGTTTT | 10 | a0001c0001t0001g0220 a0001c0001t0001g0317 a0001c0005t0003g0033 others(7): Show |
10 | HG02145.hp2 HG02622.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.794+2422_794+2426d others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321761 | |||||||
chr5:180321761 | GGTTTT | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(257): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.794+2422_794+2426d others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321761 | |||||||
chr5:180321761 | GGTTTTGT others(3): Show |
G | 12 | a0001c0001t0001g0035 a0001c0001t0001g0124 a0001c0001t0001g0233 others(9): Show |
13 | HG00639.hp1 HG01099.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.794+2417_794+2426d others(12): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321761 | |||||||
chr5:180321761 | GGTTTTGT others(8): Show |
G | 21 | a0001c0001t0001g0263 a0001c0003t0001g0198 a0001c0003t0001g0243 others(18): Show |
23 | HG00099.hp1 HG01433.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.794+2412_794+2426d others(17): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321761 | |||||||
chr5:180321783 | TTTTGTTT others(7): Show |
T | 1 | a0003c0006t0006g0181 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.794+2391_794+2404d others(16): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321783 | |||||||
chr5:180321806 | C | T | 8 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0071 others(5): Show |
10 | HG00438.hp1 HG00597.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.794+2382G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321806 | |||||||
chr5:180321815 | G | A | 1 | a0001c0004t0001g0060 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.794+2373C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321815 | |||||||
chr5:180321822 | T | C | 4 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0005t0001g0219 others(1): Show |
4 | HG02258.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+2366A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321822 | |||||||
chr5:180321823 | G | A | 3 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0005t0001g0219 |
3 | HG02630.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.794+2365C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321823 | |||||||
chr5:180321901 | A | G | 2 | a0001c0001t0001g0345 a0001c0004t0001g0344 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.794+2287T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321901 | |||||||
chr5:180321929 | C | G | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2259G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321929 | |||||||
chr5:180321930 | T | C | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2258A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321930 | |||||||
chr5:180321935 | C | T | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2253G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321935 | |||||||
chr5:180321949 | G | A | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2239C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321949 | |||||||
chr5:180321975 | A | G | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2213T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321975 | |||||||
chr5:180321978 | C | G | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2210G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321978 | |||||||
chr5:180321989 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.794+2199C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321989 | |||||||
chr5:180321994 | G | A | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2194C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321994 | |||||||
chr5:180321998 | A | C | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2190T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180321998 | |||||||
chr5:180322002 | T | C | 1 | a0001c0001t0005g0365 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.794+2186A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322002 | |||||||
chr5:180322019 | T | C | 2 | a0001c0001t0005g0377 a0001c0005t0003g0214 |
2 | HG02071.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.794+2169A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322019 | |||||||
chr5:180322023 | A | G | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2165T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322023 | |||||||
chr5:180322029 | T | C | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2159A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322029 | |||||||
chr5:180322030 | G | A | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2158C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322030 | |||||||
chr5:180322031 | T | C | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2157A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322031 | |||||||
chr5:180322054 | T | C | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2134A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322054 | |||||||
chr5:180322060 | G | T | 1 | a0001c0005t0003g0214 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.794+2128C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322060 | |||||||
chr5:180322067 | G | A | 2 | a0001c0001t0005g0367 a0001c0004t0005g0366 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.794+2121C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322067 | |||||||
chr5:180322260 | G | A | 2 | a0001c0001t0001g0345 a0001c0004t0001g0344 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.794+1928C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322260 | |||||||
chr5:180322357 | T | C | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.794+1831A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322357 | |||||||
chr5:180322510 | A | G | 1 | a0001c0001t0005g0377 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.794+1678T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322510 | |||||||
chr5:180322546 | A | G | 5 | a0001c0001t0005g0365 a0001c0005t0007g0267 a0002c0002t0004g0025 others(2): Show |
6 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+1642T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322546 | |||||||
chr5:180322604 | G | A | 3 | a0001c0001t0001g0326 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG01109.hp1 HG01123.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.794+1584C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322604 | |||||||
chr5:180322728 | C | CT | 4 | a0001c0001t0001g0345 a0001c0004t0001g0005 a0001c0004t0001g0344 others(1): Show |
5 | HG02818.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+1459dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322728 | |||||||
chr5:180322736 | T | A | 3 | a0001c0004t0001g0060 a0003c0006t0001g0241 a0003c0006t0001g0242 |
3 | NA18968.hp2 NA18995.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.794+1452A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322736 | |||||||
chr5:180322736 | T | TA | 18 | a0001c0001t0001g0263 a0001c0003t0001g0243 a0001c0004t0005g0373 others(15): Show |
19 | HG00099.hp1 HG01433.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.794+1451dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322736 | |||||||
chr5:180322737 | A | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(155): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.794+1451T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322737 | |||||||
chr5:180322738 | A | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0262 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.794+1450T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322738 | |||||||
chr5:180322861 | C | A | 1 | a0002c0008t0001g0226 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.794+1327G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322861 | |||||||
chr5:180322905 | G | A | 11 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0005g0363 others(8): Show |
11 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.794+1283C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322905 | |||||||
chr5:180322967 | G | A | 1 | a0001c0003t0001g0254 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.794+1221C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322967 | |||||||
chr5:180322984 | G | A | 38 | a0001c0001t0001g0016 a0001c0001t0001g0158 a0001c0001t0001g0193 others(35): Show |
39 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.794+1204C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180322984 | |||||||
chr5:180323237 | G | A | 1 | a0001c0005t0003g0172 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.794+951C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323237 | |||||||
chr5:180323315 | G | A | 3 | a0001c0001t0001g0345 a0001c0004t0001g0005 a0001c0004t0001g0344 |
4 | HG02818.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.794+873C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323315 | |||||||
chr5:180323336 | C | T | 16 | a0001c0003t0001g0243 a0001c0018t0006g0308 a0002c0002t0002g0034 others(13): Show |
16 | HG01975.hp1 HG03239.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.794+852G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323336 | |||||||
chr5:180323337 | G | A | 75 | a0001c0001t0001g0019 a0001c0001t0001g0176 a0001c0001t0001g0246 others(72): Show |
81 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.794+851C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323337 | |||||||
chr5:180323381 | C | G | 1 | a0001c0004t0005g0373 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.794+807G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323381 | |||||||
chr5:180323489 | A | G | 2 | a0001c0001t0001g0019 a0001c0003t0001g0271 |
3 | HG01433.hp1 HG03490.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.794+699T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323489 | |||||||
chr5:180323550 | G | C | 1 | a0001c0001t0001g0284 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.794+638C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180323550 | |||||||
chr5:180324111 | A | G | 119 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(116): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.794+77T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 9/18 | chr5 | 180324111 | |||||||
chr5:180324318 | G | C | 1 | a0001c0005t0007g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.677-13C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324318 | |||||||
chr5:180324356 | A | C | 4 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0005t0001g0219 others(1): Show |
4 | HG02630.hp1 HG03195.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.677-51T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324356 | |||||||
chr5:180324390 | A | G | 52 | a0001c0001t0001g0233 a0001c0003t0001g0064 a0001c0003t0001g0065 others(49): Show |
56 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.677-85T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324390 | |||||||
chr5:180324402 | G | T | 9 | a0001c0003t0001g0105 a0002c0002t0002g0011 a0002c0002t0002g0078 others(6): Show |
10 | HG02135.hp1 HG02165.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.677-97C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324402 | |||||||
chr5:180324441 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(39): Show |
48 | HG00140.hp2 HG01167.hp2 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.677-136G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324441 | |||||||
chr5:180324653 | T | C | 1 | a0001c0005t0021g0368 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.676+163A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324653 | |||||||
chr5:180324763 | G | A | 1 | a0001c0001t0005g0365 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.676+53C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 8/18 | chr5 | 180324763 | |||||||
chr5:180325031 | C | T | 34 | a0001c0001t0001g0158 a0001c0001t0001g0193 a0001c0001t0001g0194 others(31): Show |
34 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.597-136G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325031 | |||||||
chr5:180325036 | G | A | 1 | a0001c0005t0001g0219 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.597-141C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325036 | |||||||
chr5:180325091 | A | T | 3 | a0001c0001t0005g0365 a0001c0001t0005g0367 a0001c0004t0005g0366 |
3 | HG02809.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.597-196T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325091 | |||||||
chr5:180325188 | C | T | 3 | a0002c0002t0004g0025 a0002c0002t0004g0348 a0002c0002t0004g0349 |
4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-293G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325188 | |||||||
chr5:180325205 | G | A | 1 | a0001c0005t0019g0361 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.597-310C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325205 | |||||||
chr5:180325215 | C | T | 195 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0111 others(192): Show |
211 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.597-320G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325215 | |||||||
chr5:180325277 | G | A | 17 | a0001c0003t0001g0243 a0001c0004t0005g0373 a0001c0018t0006g0308 others(14): Show |
17 | HG01975.hp1 HG02451.hp1 HG03239.hp2 others(14): Show |
intron_variant | MODIFIER | c.597-382C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325277 | |||||||
chr5:180325367 | C | G | 1 | a0001c0005t0003g0125 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.597-472G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325367 | |||||||
chr5:180325477 | G | A | 40 | a0001c0001t0001g0158 a0001c0001t0001g0193 a0001c0001t0001g0194 others(37): Show |
41 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.597-582C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325477 | |||||||
chr5:180325504 | C | T | 1 | a0002c0002t0012g0026 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.597-609G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325504 | |||||||
chr5:180325506 | C | T | 1 | a0001c0005t0021g0368 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.597-611G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325506 | |||||||
chr5:180325680 | C | T | 3 | a0001c0009t0001g0180 a0001c0009t0001g0356 a0001c0009t0005g0375 |
3 | HG02145.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.597-785G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325680 | |||||||
chr5:180325751 | G | A | 3 | a0002c0002t0004g0025 a0002c0002t0004g0348 a0002c0002t0004g0349 |
4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-856C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325751 | |||||||
chr5:180325784 | T | C | 18 | a0001c0001t0001g0263 a0001c0003t0001g0243 a0001c0018t0006g0308 others(15): Show |
19 | HG00099.hp1 HG01433.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.597-889A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325784 | |||||||
chr5:180325797 | C | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0208 |
4 | HG01884.hp2 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.597-902G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325797 | |||||||
chr5:180325896 | G | A | 2 | a0001c0003t0001g0301 a0001c0004t0001g0005 |
3 | HG00558.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.597-1001C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180325896 | |||||||
chr5:180326003 | C | T | 2 | a0001c0003t0001g0203 a0001c0004t0001g0204 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.597-1108G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326003 | |||||||
chr5:180326024 | C | CTAAA | 130 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0233 others(127): Show |
140 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.597-1133_597-1130d others(6): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326024 | |||||||
chr5:180326024 | C | CTAAATAA others(1): Show |
6 | a0001c0001t0001g0196 a0001c0004t0001g0055 a0001c0004t0005g0373 others(3): Show |
6 | HG02071.hp1 HG02451.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.597-1137_597-1130d others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326024 | |||||||
chr5:180326024 | CTAAATAA others(1): Show |
C | 5 | a0001c0001t0001g0345 a0001c0004t0001g0005 a0001c0004t0001g0344 others(2): Show |
6 | HG02486.hp2 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.597-1137_597-1130d others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326024 | |||||||
chr5:180326119 | T | C | 320 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(317): Show |
345 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.597-1224A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326119 | |||||||
chr5:180326179 | A | T | 1 | a0001c0005t0002g0082 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.597-1284T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326179 | |||||||
chr5:180326185 | G | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(251): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.597-1290C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326185 | |||||||
chr5:180326218 | G | T | 53 | a0001c0001t0001g0233 a0001c0003t0001g0064 a0001c0003t0001g0065 others(50): Show |
57 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.597-1323C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326218 | |||||||
chr5:180326220 | A | T | 53 | a0001c0001t0001g0233 a0001c0003t0001g0064 a0001c0003t0001g0065 others(50): Show |
57 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.597-1325T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326220 | |||||||
chr5:180326221 | A | T | 53 | a0001c0001t0001g0233 a0001c0003t0001g0064 a0001c0003t0001g0065 others(50): Show |
57 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.597-1326T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326221 | |||||||
chr5:180326305 | T | C | 2 | a0001c0005t0010g0360 a0001c0005t0010g0362 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.597-1410A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326305 | |||||||
chr5:180326375 | G | C | 2 | a0001c0005t0010g0360 a0001c0005t0010g0362 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.597-1480C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326375 | |||||||
chr5:180326418 | T | G | 1 | a0001c0005t0021g0368 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.597-1523A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326418 | |||||||
chr5:180326498 | CAAT | C | 20 | a0001c0001t0001g0158 a0001c0005t0004g0045 a0001c0005t0004g0058 others(17): Show |
20 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.597-1606_597-1604d others(5): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180326498 | |||||||
chr5:180327006 | G | A | 2 | a0001c0004t0001g0134 a0001c0004t0001g0270 |
2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.596+1271C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327006 | |||||||
chr5:180327131 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.596+1146C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327131 | |||||||
chr5:180327236 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.596+1041C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327236 | |||||||
chr5:180327291 | C | T | 74 | a0001c0001t0001g0019 a0001c0001t0001g0176 a0001c0001t0001g0246 others(71): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.596+986G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327291 | |||||||
chr5:180327373 | C | A | 69 | a0001c0001t0001g0035 a0001c0001t0001g0111 a0001c0001t0001g0115 others(66): Show |
75 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.596+904G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327373 | |||||||
chr5:180327576 | T | C | 2 | a0001c0001t0001g0123 a0001c0005t0011g0379 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.596+701A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327576 | |||||||
chr5:180327657 | T | C | 143 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0158 others(140): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.596+620A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327657 | |||||||
chr5:180327664 | T | C | 1 | a0002c0002t0002g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.596+613A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327664 | |||||||
chr5:180327685 | G | A | 1 | a0001c0004t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.596+592C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327685 | |||||||
chr5:180327687 | T | C | 1 | a0004c0011t0002g0012 | 2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.596+590A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327687 | |||||||
chr5:180327715 | C | A | 2 | a0001c0003t0001g0203 a0001c0004t0001g0204 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.596+562G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327715 | |||||||
chr5:180327758 | C | T | 16 | a0001c0003t0001g0243 a0001c0018t0006g0308 a0002c0002t0002g0034 others(13): Show |
16 | HG01975.hp1 HG03239.hp2 HG04199.hp2 others(13): Show |
intron_variant | MODIFIER | c.596+519G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327758 | |||||||
chr5:180327776 | T | C | 6 | a0001c0001t0001g0345 a0001c0004t0001g0005 a0001c0004t0001g0309 others(3): Show |
7 | HG02074.hp1 HG02486.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.596+501A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180327776 | |||||||
chr5:180328071 | C | CT | 18 | a0001c0001t0001g0263 a0001c0003t0001g0243 a0001c0005t0021g0368 others(15): Show |
19 | HG00099.hp1 HG01433.hp2 HG03239.hp1 others(16): Show |
intron_variant | MODIFIER | c.596+205dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328071 | |||||||
chr5:180328071 | CT | C | 68 | a0001c0001t0001g0023 a0001c0001t0001g0233 a0001c0001t0001g0282 others(65): Show |
74 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.596+205delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328071 | |||||||
chr5:180328107 | C | T | 2 | a0001c0005t0010g0360 a0001c0005t0010g0362 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.596+170G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328107 | |||||||
chr5:180328118 | G | C | 18 | a0001c0001t0001g0263 a0001c0003t0001g0243 a0001c0018t0006g0308 others(15): Show |
19 | HG00099.hp1 HG01433.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.596+159C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328118 | |||||||
chr5:180328185 | G | A | 2 | a0001c0001t0005g0367 a0001c0004t0005g0366 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.596+92C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328185 | |||||||
chr5:180328207 | C | T | 1 | a0002c0002t0002g0135 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.596+70G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 7/18 | chr5 | 180328207 | |||||||
chr5:180328559 | C | T | 21 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0005g0363 others(18): Show |
21 | HG00280.hp1 HG01167.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.535-221G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180328559 | |||||||
chr5:180328744 | G | A | 1 | a0001c0004t0005g0373 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.535-406C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180328744 | |||||||
chr5:180328805 | T | G | 1 | a0001c0001t0009g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.535-467A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180328805 | |||||||
chr5:180328873 | A | G | 38 | a0001c0001t0001g0016 a0001c0001t0001g0158 a0001c0001t0001g0193 others(35): Show |
39 | HG00609.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.535-535T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180328873 | |||||||
chr5:180328973 | G | A | 5 | a0001c0001t0001g0345 a0001c0004t0001g0005 a0001c0004t0001g0344 others(2): Show |
6 | HG02486.hp2 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-635C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180328973 | |||||||
chr5:180329001 | C | T | 70 | a0001c0001t0001g0035 a0001c0001t0001g0111 a0001c0001t0001g0115 others(67): Show |
76 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.535-663G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329001 | |||||||
chr5:180329044 | T | C | 1 | a0002c0002t0002g0078 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.535-706A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329044 | |||||||
chr5:180329207 | C | T | 3 | a0001c0001t0001g0220 a0001c0003t0001g0274 a0001c0012t0001g0091 |
3 | HG03471.hp2 NA19011.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.535-869G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329207 | |||||||
chr5:180329208 | G | A | 54 | a0001c0001t0001g0233 a0001c0003t0001g0064 a0001c0003t0001g0065 others(51): Show |
58 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.535-870C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329208 | |||||||
chr5:180329224 | G | A | 2 | a0001c0005t0010g0360 a0001c0005t0010g0362 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.535-886C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329224 | |||||||
chr5:180329483 | G | C | 2 | a0001c0005t0010g0360 a0001c0005t0010g0362 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.535-1145C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329483 | |||||||
chr5:180329804 | G | A | 1 | a0001c0004t0001g0056 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.534+896C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329804 | |||||||
chr5:180329809 | G | C | 1 | a0001c0005t0003g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.534+891C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329809 | |||||||
chr5:180329818 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0099 others(24): Show |
32 | HG00140.hp2 HG01255.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.534+882G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329818 | |||||||
chr5:180329826 | C | T | 1 | a0002c0002t0002g0078 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.534+874G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329826 | |||||||
chr5:180329994 | G | A | 3 | a0002c0002t0004g0025 a0002c0002t0004g0348 a0002c0002t0004g0349 |
4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.534+706C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180329994 | |||||||
chr5:180330031 | A | C | 1 | a0001c0005t0007g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.534+669T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330031 | |||||||
chr5:180330031 | A | G | 18 | a0001c0001t0001g0263 a0001c0003t0001g0243 a0001c0018t0006g0308 others(15): Show |
19 | HG00099.hp1 HG01433.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.534+669T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330031 | |||||||
chr5:180330073 | C | T | 1 | a0001c0003t0001g0278 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.534+627G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330073 | |||||||
chr5:180330187 | G | A | 1 | a0001c0004t0001g0062 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.534+513C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330187 | |||||||
chr5:180330188 | G | C | 7 | a0001c0004t0001g0223 a0001c0004t0001g0224 a0001c0004t0001g0225 others(4): Show |
7 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+512C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330188 | |||||||
chr5:180330191 | C | T | 1 | a0001c0003t0001g0303 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.534+509G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330191 | |||||||
chr5:180330470 | T | C | 7 | a0001c0004t0001g0223 a0001c0004t0001g0224 a0001c0004t0001g0225 others(4): Show |
7 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.534+230A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330470 | |||||||
chr5:180330486 | C | T | 1 | a0002c0002t0002g0032 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.534+214G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330486 | |||||||
chr5:180330675 | T | G | 5 | a0002c0002t0002g0081 a0002c0002t0002g0138 a0002c0002t0002g0215 others(2): Show |
5 | HG00140.hp2 HG01516.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.534+25A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 6/18 | chr5 | 180330675 | |||||||
chr5:180330883 | C | T | 1 | a0001c0001t0005g0367 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.400-49G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180330883 | |||||||
chr5:180331012 | C | T | 4 | a0001c0004t0001g0068 a0002c0002t0002g0087 a0002c0002t0002g0095 others(1): Show |
4 | HG00609.hp2 HG02040.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-178G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331012 | |||||||
chr5:180331045 | C | T | 8 | a0001c0001t0001g0345 a0001c0001t0005g0367 a0001c0004t0001g0005 others(5): Show |
9 | HG02486.hp2 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-211G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331045 | |||||||
chr5:180331046 | A | G | 8 | a0001c0001t0001g0345 a0001c0001t0005g0367 a0001c0004t0001g0005 others(5): Show |
9 | HG02486.hp2 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-212T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331046 | |||||||
chr5:180331067 | A | G | 8 | a0001c0001t0001g0345 a0001c0001t0005g0367 a0001c0004t0001g0005 others(5): Show |
9 | HG02145.hp1 HG02486.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-233T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331067 | |||||||
chr5:180331178 | C | T | 1 | a0002c0002t0002g0081 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.399+317G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331178 | |||||||
chr5:180331189 | C | T | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.399+306G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331189 | |||||||
chr5:180331205 | G | A | 1 | a0001c0003t0001g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.399+290C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331205 | |||||||
chr5:180331295 | A | G | 4 | a0001c0001t0001g0284 a0001c0004t0001g0217 a0001c0004t0001g0218 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+200T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331295 | |||||||
chr5:180331323 | T | C | 21 | a0001c0001t0009g0169 a0001c0003t0001g0230 a0001c0003t0001g0277 others(18): Show |
21 | HG00558.hp1 HG02145.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.399+172A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 5/18 | chr5 | 180331323 | |||||||
chr5:180331608 | T | A | 1 | a0001c0004t0005g0373 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.341-55A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331608 | |||||||
chr5:180331710 | G | A | 3 | a0001c0004t0001g0005 a0001c0005t0010g0360 a0001c0005t0010g0362 |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-157C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331710 | |||||||
chr5:180331760 | G | T | 1 | a0001c0004t0001g0154 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.341-207C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331760 | |||||||
chr5:180331853 | C | T | 1 | a0001c0003t0001g0175 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.341-300G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331853 | |||||||
chr5:180331920 | A | G | 10 | a0001c0003t0001g0221 a0001c0004t0001g0223 a0001c0004t0001g0224 others(7): Show |
10 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.341-367T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331920 | |||||||
chr5:180331921 | A | G | 10 | a0001c0003t0001g0221 a0001c0004t0001g0223 a0001c0004t0001g0224 others(7): Show |
10 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.341-368T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331921 | |||||||
chr5:180331962 | G | T | 3 | a0001c0004t0001g0005 a0001c0005t0010g0360 a0001c0005t0010g0362 |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-409C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331962 | |||||||
chr5:180331985 | G | A | 2 | a0001c0001t0001g0342 a0001c0005t0001g0341 |
2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.341-432C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180331985 | |||||||
chr5:180332077 | A | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0248 a0002c0002t0013g0027 |
3 | HG02602.hp1 HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.341-524T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332077 | |||||||
chr5:180332246 | C | T | 2 | a0005c0010t0001g0132 a0005c0010t0001g0133 |
2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.341-693G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332246 | |||||||
chr5:180332251 | G | A | 1 | a0001c0005t0005g0371 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-698C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332251 | |||||||
chr5:180332256 | AGGGGGAT others(2): Show |
A | 32 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0193 others(29): Show |
33 | HG00099.hp1 HG00280.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.341-712_341-704del others(9): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332256 | |||||||
chr5:180332265 | C | T | 6 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0072 others(3): Show |
6 | HG00438.hp1 NA18941.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-712G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332265 | |||||||
chr5:180332282 | G | T | 1 | a0001c0003t0001g0347 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.341-729C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332282 | |||||||
chr5:180332314 | A | G | 5 | a0001c0001t0001g0284 a0001c0004t0001g0217 a0001c0004t0001g0218 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-761T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332314 | |||||||
chr5:180332316 | G | A | 5 | a0001c0001t0001g0284 a0001c0004t0001g0217 a0001c0004t0001g0218 others(2): Show |
5 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-763C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332316 | |||||||
chr5:180332477 | C | T | 6 | a0001c0001t0001g0284 a0001c0004t0001g0134 a0001c0004t0001g0217 others(3): Show |
6 | HG02451.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-924G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332477 | |||||||
chr5:180332496 | A | AT | 6 | a0001c0001t0001g0284 a0001c0004t0001g0134 a0001c0004t0001g0217 others(3): Show |
6 | HG02451.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-944dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332496 | |||||||
chr5:180332526 | A | G | 3 | a0003c0006t0001g0235 a0003c0006t0001g0236 a0003c0006t0001g0237 |
3 | NA18946.hp1 NA19068.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.341-973T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332526 | |||||||
chr5:180332668 | G | T | 1 | a0002c0002t0002g0081 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.341-1115C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332668 | |||||||
chr5:180332698 | C | T | 3 | a0002c0002t0004g0025 a0002c0002t0004g0348 a0002c0002t0004g0349 |
4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-1145G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332698 | |||||||
chr5:180332721 | G | A | 1 | a0001c0001t0001g0329 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.341-1168C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332721 | |||||||
chr5:180332760 | G | A | 1 | a0001c0004t0001g0042 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.341-1207C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332760 | |||||||
chr5:180332810 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG00323.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.341-1257C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332810 | |||||||
chr5:180332928 | T | C | 71 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0193 others(68): Show |
74 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.341-1375A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180332928 | |||||||
chr5:180333013 | C | T | 27 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0193 others(24): Show |
27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.341-1460G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333013 | |||||||
chr5:180333120 | T | C | 22 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0208 others(19): Show |
23 | HG00140.hp2 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.341-1567A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333120 | |||||||
chr5:180333129 | C | A | 1 | a0001c0001t0001g0261 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.341-1576G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333129 | |||||||
chr5:180333239 | CT | C | 44 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(41): Show |
47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.341-1687delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333239 | |||||||
chr5:180333298 | G | A | 1 | a0001c0004t0005g0373 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.341-1745C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333298 | |||||||
chr5:180333352 | C | T | 1 | a0002c0002t0004g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.341-1799G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333352 | |||||||
chr5:180333398 | C | T | 1 | a0002c0002t0004g0168 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.341-1845G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333398 | |||||||
chr5:180333463 | C | T | 1 | a0001c0004t0001g0014 | 2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.341-1910G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333463 | |||||||
chr5:180333481 | G | A | 1 | a0001c0004t0008g0029 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.341-1928C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333481 | |||||||
chr5:180333481 | G | T | 3 | a0001c0004t0001g0005 a0001c0005t0010g0360 a0001c0005t0010g0362 |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-1928C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333481 | |||||||
chr5:180333525 | T | C | 44 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(41): Show |
47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.341-1972A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333525 | |||||||
chr5:180333548 | TTTACA | T | 4 | a0001c0003t0001g0278 a0001c0003t0001g0296 a0001c0003t0001g0310 others(1): Show |
4 | NA18612.hp2 NA18941.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-2000_341-1996d others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333548 | |||||||
chr5:180333567 | T | C | 2 | a0001c0001t0005g0367 a0001c0004t0005g0366 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.341-2014A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333567 | |||||||
chr5:180333593 | C | T | 27 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0193 others(24): Show |
27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.341-2040G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333593 | |||||||
chr5:180333595 | A | T | 44 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(41): Show |
47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.341-2042T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333595 | |||||||
chr5:180333682 | C | T | 41 | a0001c0001t0001g0158 a0001c0001t0001g0248 a0001c0003t0001g0243 others(38): Show |
42 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.341-2129G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333682 | |||||||
chr5:180333982 | G | C | 1 | a0001c0005t0021g0368 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.340+1846C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180333982 | |||||||
chr5:180334163 | G | C | 286 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(283): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.340+1665C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334163 | |||||||
chr5:180334182 | C | T | 1 | a0001c0003t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.340+1646G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334182 | |||||||
chr5:180334248 | G | T | 44 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(41): Show |
47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.340+1580C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334248 | |||||||
chr5:180334279 | T | A | 9 | a0001c0003t0001g0221 a0001c0004t0001g0223 a0001c0004t0001g0224 others(6): Show |
9 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+1549A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334279 | |||||||
chr5:180334366 | C | A | 3 | a0001c0001t0001g0284 a0001c0003t0001g0335 a0001c0003t0014g0336 |
3 | HG02451.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.340+1462G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334366 | |||||||
chr5:180334424 | C | T | 1 | a0001c0005t0004g0130 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.340+1404G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334424 | |||||||
chr5:180334454 | G | C | 40 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(37): Show |
42 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.340+1374C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334454 | |||||||
chr5:180334499 | A | G | 1 | a0001c0004t0001g0062 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.340+1329T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334499 | |||||||
chr5:180334609 | A | G | 6 | a0001c0001t0001g0284 a0001c0004t0001g0134 a0001c0004t0001g0217 others(3): Show |
6 | HG02451.hp2 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+1219T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334609 | |||||||
chr5:180334739 | C | T | 1 | a0002c0002t0002g0080 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.340+1089G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334739 | |||||||
chr5:180334769 | C | T | 44 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(41): Show |
47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.340+1059G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334769 | |||||||
chr5:180334985 | G | A | 9 | a0001c0003t0001g0221 a0001c0004t0001g0223 a0001c0004t0001g0224 others(6): Show |
9 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+843C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180334985 | |||||||
chr5:180335097 | A | G | 286 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(283): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.340+731T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335097 | |||||||
chr5:180335254 | A | G | 1 | a0001c0004t0001g0352 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.340+574T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335254 | |||||||
chr5:180335289 | C | T | 41 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(38): Show |
43 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.340+539G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335289 | |||||||
chr5:180335360 | C | G | 199 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(196): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.340+468G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335360 | |||||||
chr5:180335405 | T | C | 44 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(41): Show |
47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.340+423A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335405 | |||||||
chr5:180335414 | G | A | 1 | a0002c0002t0002g0032 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.340+414C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335414 | |||||||
chr5:180335590 | G | A | 3 | a0002c0002t0002g0343 a0003c0014t0001g0292 a0003c0014t0001g0302 |
3 | NA18946.hp2 NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.340+238C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335590 | |||||||
chr5:180335601 | C | T | 1 | a0001c0003t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.340+227G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335601 | |||||||
chr5:180335752 | C | A | 1 | a0001c0005t0004g0130 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.340+76G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335752 | |||||||
chr5:180335799 | C | T | 1 | a0001c0005t0001g0219 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.340+29G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335799 | |||||||
chr5:180335808 | C | T | 1 | a0001c0004t0001g0344 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.340+20G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 4/18 | chr5 | 180335808 | |||||||
chr5:180336018 | C | T | 27 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0193 others(24): Show |
27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.215-65G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336018 | |||||||
chr5:180336149 | G | C | 1 | a0003c0006t0001g0245 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.215-196C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336149 | |||||||
chr5:180336175 | G | C | 1 | a0001c0005t0003g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.215-222C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336175 | |||||||
chr5:180336290 | G | A | 40 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(37): Show |
42 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.214+189C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336290 | |||||||
chr5:180336293 | G | A | 1 | a0002c0002t0002g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.214+186C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336293 | |||||||
chr5:180336306 | A | G | 1 | a0002c0002t0002g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.214+173T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336306 | |||||||
chr5:180336316 | C | T | 3 | a0001c0004t0001g0005 a0001c0005t0010g0360 a0001c0005t0010g0362 |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.214+163G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336316 | |||||||
chr5:180336319 | T | C | 11 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0004t0001g0068 others(8): Show |
13 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.214+160A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336319 | |||||||
chr5:180336398 | T | G | 286 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(283): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.214+81A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 3/18 | chr5 | 180336398 | |||||||
chr5:180336768 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0208 |
4 | HG01884.hp2 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-191T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336768 | |||||||
chr5:180336776 | G | A | 2 | a0001c0001t0001g0345 a0001c0004t0001g0344 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.116-199C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336776 | |||||||
chr5:180336789 | C | T | 52 | a0001c0001t0001g0019 a0001c0003t0001g0002 a0001c0003t0001g0018 others(49): Show |
58 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.116-212G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336789 | |||||||
chr5:180336876 | G | A | 27 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0193 others(24): Show |
27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.116-299C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336876 | |||||||
chr5:180336923 | T | C | 44 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(41): Show |
47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.116-346A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336923 | |||||||
chr5:180336935 | G | A | 1 | a0001c0003t0001g0243 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.116-358C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336935 | |||||||
chr5:180336952 | G | A | 3 | a0001c0004t0001g0005 a0001c0005t0010g0360 a0001c0005t0010g0362 |
4 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-375C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180336952 | |||||||
chr5:180337123 | C | T | 2 | a0001c0001t0001g0345 a0001c0004t0001g0344 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.116-546G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337123 | |||||||
chr5:180337124 | G | A | 1 | a0002c0015t0001g0013 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.116-547C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337124 | |||||||
chr5:180337176 | C | T | 7 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0071 others(4): Show |
9 | HG00438.hp1 HG00597.hp1 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.116-599G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337176 | |||||||
chr5:180337209 | C | T | 1 | a0001c0005t0004g0149 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.116-632G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337209 | |||||||
chr5:180337270 | C | T | 41 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(38): Show |
43 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.116-693G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337270 | |||||||
chr5:180337271 | G | A | 1 | a0001c0005t0004g0291 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.116-694C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337271 | |||||||
chr5:180337322 | G | C | 1 | a0001c0004t0001g0188 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.116-745C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337322 | |||||||
chr5:180337370 | G | A | 7 | a0001c0005t0003g0033 a0001c0005t0003g0088 a0001c0005t0003g0265 others(4): Show |
7 | HG02145.hp2 HG02622.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.116-793C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337370 | |||||||
chr5:180337378 | A | G | 1 | a0002c0002t0002g0135 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.116-801T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337378 | |||||||
chr5:180337453 | G | GAAA | 40 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(37): Show |
42 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.116-879_116-877dup others(3): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337453 | |||||||
chr5:180337453 | GA | G | 12 | a0001c0001t0001g0273 a0001c0005t0003g0033 a0001c0005t0003g0088 others(9): Show |
13 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.116-877delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337453 | |||||||
chr5:180337488 | C | T | 1 | a0002c0002t0004g0168 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.116-911G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337488 | |||||||
chr5:180337586 | C | T | 2 | a0001c0004t0001g0217 a0001c0004t0001g0218 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.115+907G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337586 | |||||||
chr5:180337612 | G | A | 1 | a0003c0014t0001g0292 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.115+881C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337612 | |||||||
chr5:180337616 | G | A | 1 | a0001c0005t0004g0165 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.115+877C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337616 | |||||||
chr5:180337621 | A | G | 2 | a0001c0003t0001g0203 a0001c0004t0001g0204 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.115+872T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337621 | |||||||
chr5:180337660 | GCCACCTC others(9): Show |
G | 27 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0193 others(24): Show |
27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.115+817_115+832del others(16): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337660 | |||||||
chr5:180337678 | G | A | 27 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0193 others(24): Show |
27 | HG00280.hp1 HG01167.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.115+815C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337678 | |||||||
chr5:180337698 | C | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0021 others(113): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.115+795G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337698 | |||||||
chr5:180337709 | T | C | 1 | a0001c0005t0021g0368 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.115+784A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337709 | |||||||
chr5:180337779 | C | T | 4 | a0001c0003t0001g0278 a0001c0003t0001g0296 a0001c0003t0001g0310 others(1): Show |
4 | NA18612.hp2 NA18941.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+714G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337779 | |||||||
chr5:180337926 | C | T | 3 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0005t0001g0219 |
3 | HG02630.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.115+567G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180337926 | |||||||
chr5:180338019 | A | C | 44 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(41): Show |
47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.115+474T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338019 | |||||||
chr5:180338021 | G | A | 1 | a0002c0002t0017g0357 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.115+472C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338021 | |||||||
chr5:180338104 | A | G | 44 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(41): Show |
47 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.115+389T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338104 | |||||||
chr5:180338291 | G | A | 1 | a0001c0003t0001g0057 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.115+202C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338291 | |||||||
chr5:180338377 | C | T | 1 | a0001c0004t0001g0309 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.115+116G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338377 | |||||||
chr5:180338413 | AC | A | 8 | a0001c0001t0005g0363 a0001c0001t0005g0364 a0001c0001t0005g0377 others(5): Show |
9 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+79delG | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338413 | |||||||
chr5:180338467 | C | T | 168 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0021 others(165): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.115+26G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 2/18 | chr5 | 180338467 | |||||||
chr5:180338662 | G | A | 2 | a0001c0004t0001g0225 a0001c0004t0001g0229 |
2 | NA18964.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.8-62C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180338662 | |||||||
chr5:180338900 | C | T | 12 | a0001c0003t0001g0243 a0002c0002t0002g0032 a0003c0006t0001g0235 others(9): Show |
12 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-300G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180338900 | |||||||
chr5:180338949 | T | C | 4 | a0001c0004t0001g0197 a0001c0004t0001g0217 a0001c0004t0001g0218 others(1): Show |
4 | HG01952.hp2 HG02630.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-349A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180338949 | |||||||
chr5:180339061 | G | A | 1 | a0001c0004t0001g0059 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.8-461C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339061 | |||||||
chr5:180339082 | A | T | 1 | a0006c0016t0002g0044 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.8-482T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339082 | |||||||
chr5:180339107 | C | A | 1 | a0003c0006t0001g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.8-507G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339107 | |||||||
chr5:180339131 | G | A | 20 | a0001c0001t0001g0246 a0001c0001t0005g0363 a0001c0001t0005g0364 others(17): Show |
22 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.8-531C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339131 | |||||||
chr5:180339177 | C | G | 1 | a0002c0002t0002g0354 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.8-577G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339177 | |||||||
chr5:180339317 | T | A | 1 | a0001c0001t0005g0365 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8-717A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339317 | |||||||
chr5:180339329 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0124 |
2 | HG02698.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.8-729C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339329 | |||||||
chr5:180339359 | A | G | 9 | a0001c0003t0001g0221 a0001c0004t0001g0223 a0001c0004t0001g0224 others(6): Show |
9 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-759T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339359 | |||||||
chr5:180339378 | C | CA | 48 | a0001c0001t0001g0190 a0001c0001t0001g0208 a0001c0001t0001g0246 others(45): Show |
49 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.8-779dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339378 | |||||||
chr5:180339378 | C | CAA | 10 | a0001c0001t0001g0345 a0001c0001t0005g0364 a0001c0001t0005g0372 others(7): Show |
10 | HG00558.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-780_8-779dupTT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339378 | |||||||
chr5:180339378 | CA | C | 67 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(64): Show |
71 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.8-779delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339378 | |||||||
chr5:180339525 | T | C | 1 | a0001c0004t0001g0061 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.8-925A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339525 | |||||||
chr5:180339558 | G | A | 1 | a0001c0003t0001g0230 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.8-958C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339558 | |||||||
chr5:180339563 | G | A | 1 | a0001c0005t0021g0368 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-963C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339563 | |||||||
chr5:180339781 | C | T | 1 | a0002c0002t0002g0081 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.8-1181G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339781 | |||||||
chr5:180339927 | T | C | 44 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(41): Show |
46 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.8-1327A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180339927 | |||||||
chr5:180340091 | A | G | 21 | a0001c0001t0001g0246 a0001c0001t0005g0363 a0001c0001t0005g0364 others(18): Show |
23 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.8-1491T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340091 | |||||||
chr5:180340107 | G | T | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.8-1507C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340107 | |||||||
chr5:180340135 | C | T | 2 | a0001c0001t0001g0255 a0001c0004t0001g0256 |
2 | HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.8-1535G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340135 | |||||||
chr5:180340137 | G | A | 1 | a0003c0006t0001g0043 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.8-1537C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340137 | |||||||
chr5:180340184 | G | GT | 42 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(39): Show |
44 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.8-1585dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340184 | |||||||
chr5:180340190 | T | C | 1 | a0001c0004t0001g0184 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.8-1590A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340190 | |||||||
chr5:180340190 | T | G | 31 | a0001c0001t0001g0158 a0001c0001t0001g0248 a0001c0003t0001g0148 others(28): Show |
31 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.8-1590A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340190 | |||||||
chr5:180340196 | G | T | 1 | a0002c0002t0002g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.8-1596C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340196 | |||||||
chr5:180340198 | T | G | 1 | a0002c0002t0002g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.8-1598A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340198 | |||||||
chr5:180340299 | C | T | 3 | a0002c0002t0004g0025 a0002c0002t0004g0348 a0002c0002t0004g0349 |
4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1699G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340299 | |||||||
chr5:180340309 | C | A | 1 | a0001c0001t0009g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8-1709G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340309 | |||||||
chr5:180340331 | C | T | 1 | a0001c0001t0005g0380 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.8-1731G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340331 | |||||||
chr5:180340332 | G | A | 1 | a0001c0021t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.8-1732C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340332 | |||||||
chr5:180340410 | T | C | 5 | a0001c0004t0001g0005 a0002c0002t0002g0137 a0002c0002t0004g0025 others(2): Show |
7 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1810A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340410 | |||||||
chr5:180340426 | G | A | 1 | a0001c0001t0005g0365 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8-1826C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340426 | |||||||
chr5:180340511 | G | GT | 76 | a0001c0001t0001g0019 a0001c0001t0001g0208 a0001c0001t0001g0246 others(73): Show |
79 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.8-1912dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340511 | |||||||
chr5:180340511 | G | GTT | 18 | a0001c0001t0005g0376 a0001c0001t0009g0290 a0001c0003t0001g0002 others(15): Show |
21 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.8-1913_8-1912dupAA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340511 | |||||||
chr5:180340511 | GT | G | 7 | a0001c0003t0001g0230 a0001c0004t0001g0225 a0001c0004t0001g0227 others(4): Show |
7 | HG02735.hp2 HG03942.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-1912delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340511 | |||||||
chr5:180340511 | GTT | G | 41 | a0001c0001t0001g0233 a0001c0001t0005g0365 a0001c0003t0001g0046 others(38): Show |
43 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.8-1913_8-1912delAA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340511 | |||||||
chr5:180340575 | C | G | 16 | a0001c0001t0001g0246 a0001c0001t0005g0363 a0001c0001t0005g0364 others(13): Show |
16 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-1975G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340575 | |||||||
chr5:180340597 | C | T | 16 | a0001c0001t0001g0246 a0001c0001t0005g0363 a0001c0001t0005g0364 others(13): Show |
16 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-1997G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340597 | |||||||
chr5:180340605 | A | G | 62 | a0001c0001t0001g0220 a0001c0001t0001g0233 a0001c0001t0001g0246 others(59): Show |
66 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.8-2005T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340605 | |||||||
chr5:180340680 | T | C | 21 | a0001c0001t0001g0220 a0001c0001t0001g0246 a0001c0001t0005g0363 others(18): Show |
23 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.8-2080A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340680 | |||||||
chr5:180340732 | T | G | 1 | a0001c0012t0001g0170 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.8-2132A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340732 | |||||||
chr5:180340765 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.8-2165G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340765 | |||||||
chr5:180340815 | C | T | 2 | a0001c0003t0001g0285 a0001c0003t0001g0346 |
2 | NA19007.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.8-2215G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340815 | |||||||
chr5:180340970 | C | T | 1 | a0001c0001t0005g0365 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8-2370G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180340970 | |||||||
chr5:180341008 | T | A | 2 | a0001c0001t0005g0367 a0001c0004t0005g0366 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.8-2408A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341008 | |||||||
chr5:180341181 | A | G | 16 | a0001c0001t0001g0246 a0001c0001t0005g0363 a0001c0001t0005g0364 others(13): Show |
16 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-2581T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341181 | |||||||
chr5:180341184 | A | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0021 others(275): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.8-2584T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341184 | |||||||
chr5:180341193 | T | C | 1 | a0002c0002t0002g0343 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.8-2593A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341193 | |||||||
chr5:180341254 | A | G | 4 | a0001c0003t0001g0313 a0001c0003t0001g0314 a0001c0003t0001g0315 others(1): Show |
4 | HG00558.hp1 HG03710.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-2654T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341254 | |||||||
chr5:180341334 | T | G | 3 | a0001c0001t0001g0284 a0001c0003t0001g0335 a0001c0003t0014g0336 |
3 | HG02451.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.8-2734A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341334 | |||||||
chr5:180341355 | C | G | 2 | a0001c0004t0001g0217 a0001c0004t0001g0218 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.8-2755G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341355 | |||||||
chr5:180341398 | A | G | 65 | a0001c0001t0001g0019 a0001c0001t0001g0307 a0001c0001t0009g0290 others(62): Show |
71 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.8-2798T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341398 | |||||||
chr5:180341527 | A | C | 22 | a0001c0001t0001g0220 a0001c0001t0001g0246 a0001c0001t0005g0363 others(19): Show |
24 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.8-2927T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341527 | |||||||
chr5:180341599 | G | A | 20 | a0001c0001t0001g0220 a0001c0001t0005g0363 a0001c0001t0005g0364 others(17): Show |
22 | HG00280.hp1 HG01099.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.8-2999C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341599 | |||||||
chr5:180341802 | G | A | 1 | a0003c0006t0001g0245 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.8-3202C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341802 | |||||||
chr5:180341859 | C | T | 10 | a0001c0003t0001g0221 a0001c0003t0001g0230 a0001c0004t0001g0223 others(7): Show |
10 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.8-3259G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341859 | |||||||
chr5:180341911 | G | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0337 a0001c0001t0001g0338 others(2): Show |
6 | HG00735.hp1 HG01358.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-3311C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180341911 | |||||||
chr5:180342345 | C | T | 31 | a0001c0001t0001g0158 a0001c0001t0001g0248 a0001c0003t0001g0148 others(28): Show |
31 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.8-3745G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342345 | |||||||
chr5:180342378 | A | C | 2 | a0001c0003t0001g0203 a0001c0004t0001g0204 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.8-3778T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342378 | |||||||
chr5:180342407 | G | GT | 164 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(161): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.8-3808dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342407 | |||||||
chr5:180342407 | G | GTT | 30 | a0001c0001t0001g0248 a0001c0001t0001g0281 a0001c0001t0001g0282 others(27): Show |
31 | HG00099.hp2 HG00597.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.8-3809_8-3808dupAA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342407 | |||||||
chr5:180342407 | GT | G | 53 | a0001c0001t0001g0127 a0001c0001t0001g0233 a0001c0001t0005g0363 others(50): Show |
55 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.8-3808delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342407 | |||||||
chr5:180342407 | GTTTTTTT others(5): Show |
G | 1 | a0001c0005t0004g0167 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.8-3819_8-3808delAA others(10): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342407 | |||||||
chr5:180342415 | T | G | 2 | a0001c0003t0001g0203 a0001c0004t0001g0204 |
2 | HG02280.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.8-3815A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342415 | |||||||
chr5:180342415 | T | TG | 12 | a0001c0003t0001g0243 a0002c0002t0002g0032 a0003c0006t0001g0235 others(9): Show |
12 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-3816_8-3815insC | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342415 | |||||||
chr5:180342627 | C | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0273 a0001c0004t0001g0085 others(1): Show |
4 | HG01255.hp2 NA18984.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-4027G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342627 | |||||||
chr5:180342654 | C | T | 1 | a0001c0003t0001g0271 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.8-4054G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342654 | |||||||
chr5:180342658 | T | C | 11 | a0001c0001t0001g0231 a0001c0003t0001g0221 a0001c0003t0001g0230 others(8): Show |
11 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.8-4058A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342658 | |||||||
chr5:180342697 | C | G | 2 | a0001c0003t0001g0269 a0001c0004t0001g0270 |
2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.8-4097G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342697 | |||||||
chr5:180342793 | T | G | 2 | a0001c0005t0010g0360 a0001c0005t0010g0362 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.8-4193A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342793 | |||||||
chr5:180342964 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(115): Show |
129 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.8-4364C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180342964 | |||||||
chr5:180343047 | T | G | 2 | a0001c0001t0005g0372 a0001c0001t0005g0376 |
2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.8-4447A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343047 | |||||||
chr5:180343163 | G | A | 2 | a0001c0005t0005g0371 a0001c0005t0021g0368 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.8-4563C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343163 | |||||||
chr5:180343243 | C | T | 3 | a0001c0004t0005g0373 a0001c0005t0011g0374 a0001c0005t0011g0379 |
3 | HG02055.hp2 HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.8-4643G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343243 | |||||||
chr5:180343258 | C | T | 1 | a0001c0001t0005g0365 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.8-4658G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343258 | |||||||
chr5:180343554 | G | A | 12 | a0001c0003t0001g0243 a0002c0002t0002g0032 a0003c0006t0001g0235 others(9): Show |
12 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-4954C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343554 | |||||||
chr5:180343559 | T | C | 11 | a0001c0001t0001g0231 a0001c0003t0001g0221 a0001c0003t0001g0230 others(8): Show |
11 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.8-4959A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343559 | |||||||
chr5:180343656 | G | A | 1 | a0001c0003t0001g0340 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.8-5056C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343656 | |||||||
chr5:180343757 | A | G | 41 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(38): Show |
43 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.8-5157T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343757 | |||||||
chr5:180343946 | G | A | 1 | a0001c0004t0001g0062 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.8-5346C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343946 | |||||||
chr5:180343983 | C | T | 1 | a0001c0005t0011g0379 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8-5383G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180343983 | |||||||
chr5:180344273 | A | C | 1 | a0001c0009t0001g0180 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8-5673T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344273 | |||||||
chr5:180344380 | G | C | 2 | a0001c0001t0005g0367 a0001c0004t0005g0366 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.8-5780C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344380 | |||||||
chr5:180344542 | A | G | 4 | a0001c0005t0003g0265 a0001c0005t0003g0266 a0001c0005t0003g0268 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-5942T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344542 | |||||||
chr5:180344750 | G | A | 2 | a0001c0005t0005g0371 a0001c0005t0021g0368 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.8-6150C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344750 | |||||||
chr5:180344787 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.8-6187G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344787 | |||||||
chr5:180344826 | C | CT | 41 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(38): Show |
43 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.8-6227dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344826 | |||||||
chr5:180344838 | C | T | 1 | a0001c0004t0001g0171 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.8-6238G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344838 | |||||||
chr5:180344847 | G | C | 1 | a0001c0005t0021g0368 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-6247C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344847 | |||||||
chr5:180344849 | A | G | 42 | a0001c0001t0001g0233 a0001c0001t0005g0365 a0001c0003t0001g0046 others(39): Show |
44 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.8-6249T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344849 | |||||||
chr5:180344851 | C | T | 5 | a0001c0001t0005g0367 a0001c0004t0001g0217 a0001c0004t0001g0218 others(2): Show |
5 | HG02630.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-6251G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344851 | |||||||
chr5:180344882 | C | A | 1 | a0001c0003t0001g0065 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.8-6282G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344882 | |||||||
chr5:180344993 | C | T | 1 | a0001c0005t0003g0206 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.8-6393G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180344993 | |||||||
chr5:180345020 | A | T | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.8-6420T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345020 | |||||||
chr5:180345062 | C | T | 62 | a0001c0001t0001g0220 a0001c0001t0001g0233 a0001c0001t0005g0363 others(59): Show |
66 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.8-6462G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345062 | |||||||
chr5:180345087 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.8-6487G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345087 | |||||||
chr5:180345259 | C | T | 1 | a0001c0021t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.8-6659G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345259 | |||||||
chr5:180345260 | G | A | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.8-6660C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345260 | |||||||
chr5:180345316 | C | T | 1 | a0001c0005t0007g0353 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.8-6716G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345316 | |||||||
chr5:180345324 | C | T | 3 | a0001c0004t0020g0359 a0001c0005t0010g0360 a0001c0005t0010g0362 |
3 | HG02486.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.8-6724G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345324 | |||||||
chr5:180345454 | G | A | 2 | a0001c0001t0001g0345 a0001c0004t0001g0344 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.8-6854C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345454 | |||||||
chr5:180345494 | T | C | 1 | a0001c0004t0001g0177 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.8-6894A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345494 | |||||||
chr5:180345589 | C | T | 1 | a0002c0002t0002g0139 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.8-6989G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345589 | |||||||
chr5:180345618 | C | T | 1 | a0002c0002t0002g0084 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.8-7018G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345618 | |||||||
chr5:180345640 | C | G | 62 | a0001c0001t0001g0220 a0001c0001t0001g0233 a0001c0001t0005g0363 others(59): Show |
66 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.8-7040G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345640 | |||||||
chr5:180345779 | G | A | 2 | a0001c0001t0001g0345 a0001c0004t0001g0344 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.8-7179C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345779 | |||||||
chr5:180345834 | C | T | 11 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0208 others(8): Show |
12 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-7234G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345834 | |||||||
chr5:180345835 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(204): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.8-7235T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345835 | |||||||
chr5:180345954 | C | T | 1 | a0001c0004t0001g0083 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.7+7257G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345954 | |||||||
chr5:180345972 | C | T | 2 | a0001c0003t0001g0221 a0002c0002t0002g0222 |
2 | HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.7+7239G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345972 | |||||||
chr5:180345985 | C | T | 3 | a0002c0002t0004g0025 a0002c0002t0004g0348 a0002c0002t0004g0349 |
4 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+7226G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180345985 | |||||||
chr5:180346019 | A | G | 2 | a0001c0001t0009g0169 a0001c0012t0001g0170 |
2 | HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.7+7192T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346019 | |||||||
chr5:180346292 | C | G | 5 | a0001c0001t0001g0220 a0001c0004t0001g0005 a0002c0002t0004g0025 others(2): Show |
7 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+6919G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346292 | |||||||
chr5:180346543 | G | A | 3 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0005t0001g0219 |
3 | HG02630.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7+6668C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346543 | |||||||
chr5:180346558 | C | T | 1 | a0002c0002t0002g0145 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.7+6653G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346558 | |||||||
chr5:180346587 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.7+6624G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346587 | |||||||
chr5:180346667 | CGCCCCTG others(2): Show |
C | 12 | a0001c0003t0001g0243 a0002c0002t0002g0032 a0003c0006t0001g0235 others(9): Show |
12 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.7+6535_7+6543delCC others(7): Show |
GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346667 | |||||||
chr5:180346802 | C | G | 3 | a0001c0005t0003g0259 a0001c0005t0003g0260 a0001c0005t0019g0361 |
3 | HG02615.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.7+6409G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346802 | |||||||
chr5:180346857 | A | G | 65 | a0001c0001t0001g0220 a0001c0001t0001g0233 a0001c0001t0001g0246 others(62): Show |
69 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.7+6354T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346857 | |||||||
chr5:180346904 | G | T | 1 | a0002c0002t0002g0040 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.7+6307C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180346904 | |||||||
chr5:180347065 | A | C | 3 | a0001c0004t0001g0134 a0005c0010t0001g0132 a0005c0010t0001g0133 |
3 | HG02965.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7+6146T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347065 | |||||||
chr5:180347073 | G | A | 3 | a0001c0001t0001g0342 a0001c0005t0001g0341 a0001c0005t0003g0033 |
3 | HG01884.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.7+6138C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347073 | |||||||
chr5:180347139 | G | A | 1 | a0002c0002t0002g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.7+6072C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347139 | |||||||
chr5:180347201 | G | T | 1 | a0002c0002t0002g0036 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.7+6010C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347201 | |||||||
chr5:180347456 | C | A | 12 | a0001c0003t0001g0243 a0002c0002t0002g0032 a0003c0006t0001g0235 others(9): Show |
12 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.7+5755G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347456 | |||||||
chr5:180347458 | G | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0208 others(12): Show |
16 | HG00140.hp2 HG01167.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.7+5753C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347458 | |||||||
chr5:180347577 | G | A | 5 | a0001c0001t0005g0363 a0001c0001t0005g0364 a0001c0001t0005g0377 others(2): Show |
5 | HG00280.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+5634C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347577 | |||||||
chr5:180347615 | T | A | 1 | a0001c0005t0003g0131 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.7+5596A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347615 | |||||||
chr5:180347642 | T | C | 359 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(356): Show |
387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.7+5569A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347642 | |||||||
chr5:180347816 | C | T | 1 | a0002c0002t0002g0144 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.7+5395G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347816 | |||||||
chr5:180347845 | G | A | 1 | a0002c0002t0002g0343 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.7+5366C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180347845 | |||||||
chr5:180348015 | A | G | 63 | a0001c0001t0001g0220 a0001c0001t0001g0233 a0001c0001t0005g0363 others(60): Show |
67 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.7+5196T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348015 | |||||||
chr5:180348102 | C | T | 62 | a0001c0001t0001g0220 a0001c0001t0001g0233 a0001c0001t0005g0363 others(59): Show |
66 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.7+5109G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348102 | |||||||
chr5:180348121 | C | A | 4 | a0001c0001t0001g0220 a0002c0002t0004g0025 a0002c0002t0004g0348 others(1): Show |
5 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+5090G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348121 | |||||||
chr5:180348132 | G | T | 1 | a0001c0005t0005g0371 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7+5079C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348132 | |||||||
chr5:180348221 | C | T | 57 | a0001c0001t0001g0233 a0001c0001t0005g0363 a0001c0001t0005g0364 others(54): Show |
59 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.7+4990G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348221 | |||||||
chr5:180348370 | T | C | 3 | a0001c0004t0020g0359 a0001c0005t0010g0360 a0001c0005t0010g0362 |
3 | HG02486.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.7+4841A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348370 | |||||||
chr5:180348441 | C | T | 14 | a0001c0001t0005g0363 a0001c0001t0005g0364 a0001c0001t0005g0369 others(11): Show |
14 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.7+4770G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348441 | |||||||
chr5:180348463 | G | A | 5 | a0001c0001t0001g0220 a0001c0004t0001g0005 a0002c0002t0004g0025 others(2): Show |
7 | HG01099.hp1 HG01109.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+4748C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348463 | |||||||
chr5:180348541 | C | T | 1 | a0001c0004t0001g0179 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.7+4670G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348541 | |||||||
chr5:180348634 | C | T | 2 | a0001c0001t0001g0255 a0001c0004t0001g0256 |
2 | HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.7+4577G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348634 | |||||||
chr5:180348732 | C | CT | 17 | a0001c0003t0001g0243 a0001c0003t0001g0252 a0001c0003t0001g0253 others(14): Show |
17 | HG01975.hp1 HG02148.hp1 HG02735.hp1 others(14): Show |
intron_variant | MODIFIER | c.7+4478dupA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348732 | |||||||
chr5:180348732 | CT | C | 59 | a0001c0001t0001g0220 a0001c0001t0001g0233 a0001c0001t0005g0363 others(56): Show |
63 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.7+4478delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348732 | |||||||
chr5:180348792 | A | G | 2 | a0001c0005t0002g0082 a0002c0002t0002g0081 |
2 | HG01358.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.7+4419T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348792 | |||||||
chr5:180348888 | C | T | 40 | a0001c0001t0001g0233 a0001c0003t0001g0046 a0001c0003t0001g0057 others(37): Show |
42 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.7+4323G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348888 | |||||||
chr5:180348898 | C | T | 1 | a0001c0021t0001g0251 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7+4313G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348898 | |||||||
chr5:180348976 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(101): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.7+4235C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180348976 | |||||||
chr5:180349036 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(101): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.7+4175C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349036 | |||||||
chr5:180349135 | A | G | 1 | a0001c0003t0001g0178 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.7+4076T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349135 | |||||||
chr5:180349320 | A | G | 1 | a0001c0004t0001g0352 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7+3891T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349320 | |||||||
chr5:180349329 | A | T | 1 | a0001c0004t0001g0037 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.7+3882T>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349329 | |||||||
chr5:180349365 | A | C | 4 | a0001c0003t0001g0077 a0002c0002t0002g0078 a0002c0002t0002g0079 others(1): Show |
4 | NA18981.hp1 NA18994.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+3846T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349365 | |||||||
chr5:180349405 | T | C | 3 | a0001c0004t0001g0217 a0001c0004t0001g0218 a0001c0005t0001g0219 |
3 | HG02630.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7+3806A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349405 | |||||||
chr5:180349469 | C | T | 1 | a0002c0015t0001g0013 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.7+3742G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349469 | |||||||
chr5:180349496 | T | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(86): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.7+3715A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349496 | |||||||
chr5:180349514 | T | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(228): Show |
246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.7+3697A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349514 | |||||||
chr5:180349530 | T | C | 3 | a0001c0001t0005g0367 a0001c0004t0001g0134 a0001c0004t0005g0366 |
3 | HG03098.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.7+3681A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349530 | |||||||
chr5:180349561 | C | T | 1 | a0001c0005t0015g0250 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7+3650G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349561 | |||||||
chr5:180349585 | G | A | 30 | a0001c0001t0001g0158 a0001c0001t0001g0248 a0001c0003t0001g0148 others(27): Show |
30 | HG00438.hp2 HG00609.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.7+3626C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349585 | |||||||
chr5:180349600 | G | A | 1 | a0001c0003t0001g0346 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.7+3611C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349600 | |||||||
chr5:180349750 | G | A | 2 | a0001c0005t0005g0371 a0001c0005t0021g0368 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.7+3461C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349750 | |||||||
chr5:180349855 | T | C | 3 | a0001c0004t0001g0134 a0005c0010t0001g0132 a0005c0010t0001g0133 |
3 | HG02965.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.7+3356A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349855 | |||||||
chr5:180349878 | GT | G | 49 | a0001c0001t0001g0220 a0001c0001t0001g0233 a0001c0001t0005g0365 others(46): Show |
53 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.7+3332delA | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349878 | |||||||
chr5:180349891 | T | G | 3 | a0001c0001t0005g0365 a0001c0001t0005g0367 a0001c0004t0005g0366 |
3 | HG02809.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.7+3320A>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349891 | |||||||
chr5:180349986 | T | C | 1 | a0002c0002t0002g0135 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.7+3225A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180349986 | |||||||
chr5:180350127 | G | A | 13 | a0001c0001t0005g0363 a0001c0001t0005g0364 a0001c0001t0005g0369 others(10): Show |
13 | HG00280.hp1 HG02015.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.7+3084C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350127 | |||||||
chr5:180350389 | G | A | 2 | a0001c0003t0001g0064 a0001c0003t0001g0065 |
2 | HG00673.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.7+2822C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350389 | |||||||
chr5:180350517 | G | A | 8 | a0002c0002t0002g0008 a0002c0002t0002g0009 a0002c0002t0002g0071 others(5): Show |
10 | HG00438.hp1 HG00597.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+2694C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350517 | |||||||
chr5:180350655 | G | C | 1 | a0001c0003t0001g0350 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.7+2556C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350655 | |||||||
chr5:180350687 | AG | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(86): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.7+2523delC | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350687 | |||||||
chr5:180350690 | A | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(86): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.7+2521T>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350690 | |||||||
chr5:180350724 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.7+2487T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350724 | |||||||
chr5:180350804 | C | G | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7+2407G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350804 | |||||||
chr5:180350869 | T | C | 11 | a0001c0001t0001g0231 a0001c0003t0001g0221 a0001c0003t0001g0230 others(8): Show |
11 | HG02735.hp2 HG03927.hp2 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.7+2342A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350869 | |||||||
chr5:180350897 | T | C | 1 | a0002c0007t0001g0351 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.7+2314A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350897 | |||||||
chr5:180350964 | C | T | 41 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0158 others(38): Show |
43 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.7+2247G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180350964 | |||||||
chr5:180351047 | T | C | 1 | a0001c0003t0005g0378 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7+2164A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351047 | |||||||
chr5:180351098 | T | A | 59 | a0001c0001t0001g0233 a0001c0001t0005g0363 a0001c0001t0005g0364 others(56): Show |
62 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.7+2113A>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351098 | |||||||
chr5:180351151 | T | C | 1 | a0001c0005t0007g0353 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7+2060A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351151 | |||||||
chr5:180351366 | C | G | 1 | a0002c0002t0002g0142 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.7+1845G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351366 | |||||||
chr5:180351393 | C | T | 1 | a0002c0015t0001g0013 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.7+1818G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351393 | |||||||
chr5:180351423 | C | T | 1 | a0001c0003t0001g0247 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.7+1788G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351423 | |||||||
chr5:180351626 | C | T | 3 | a0001c0004t0020g0359 a0001c0005t0010g0360 a0001c0005t0010g0362 |
3 | HG02486.hp2 HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.7+1585G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351626 | |||||||
chr5:180351738 | G | A | 1 | a0001c0005t0003g0234 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.7+1473C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351738 | |||||||
chr5:180351923 | G | T | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7+1288C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180351923 | |||||||
chr5:180352124 | G | A | 13 | a0001c0003t0001g0243 a0001c0004t0008g0029 a0002c0002t0002g0032 others(10): Show |
13 | HG01975.hp1 HG03239.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.7+1087C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352124 | |||||||
chr5:180352206 | G | C | 1 | a0001c0001t0001g0246 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.7+1005C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352206 | |||||||
chr5:180352293 | C | A | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7+918G>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352293 | |||||||
chr5:180352339 | G | GA | 129 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0021 others(126): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.7+871dupT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352339 | |||||||
chr5:180352339 | GA | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(82): Show |
95 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.7+871delT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352339 | |||||||
chr5:180352339 | GAA | G | 37 | a0001c0001t0005g0365 a0001c0003t0001g0046 a0001c0003t0001g0057 others(34): Show |
39 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.7+870_7+871delTT | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352339 | |||||||
chr5:180352340 | A | G | 2 | a0002c0002t0002g0066 a0003c0006t0006g0067 |
2 | NA18959.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.7+871T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352340 | |||||||
chr5:180352341 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.7+870T>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352341 | |||||||
chr5:180352360 | G | T | 1 | a0002c0002t0002g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.7+851C>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352360 | |||||||
chr5:180352375 | T | C | 1 | a0002c0002t0002g0354 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.7+836A>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352375 | |||||||
chr5:180352506 | C | G | 1 | a0001c0005t0003g0033 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.7+705G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352506 | |||||||
chr5:180352607 | G | C | 13 | a0001c0001t0005g0363 a0001c0001t0005g0364 a0001c0001t0005g0372 others(10): Show |
13 | HG00280.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.7+604C>G | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352607 | |||||||
chr5:180352683 | C | G | 1 | a0002c0002t0002g0032 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.7+528G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352683 | |||||||
chr5:180352903 | G | A | 2 | a0001c0001t0005g0363 a0001c0001t0005g0364 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.7+308C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352903 | |||||||
chr5:180352932 | C | T | 1 | a0001c0003t0001g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.7+279G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352932 | |||||||
chr5:180352974 | G | A | 1 | a0001c0003t0001g0355 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.7+237C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180352974 | |||||||
chr5:180353056 | C | T | 1 | a0001c0003t0001g0030 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.7+155G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180353056 | |||||||
chr5:180353104 | C | G | 2 | a0001c0001t0005g0363 a0001c0001t0005g0364 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.7+107G>C | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180353104 | |||||||
chr5:180353134 | C | T | 1 | a0001c0004t0001g0005 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7+77G>A | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180353134 | |||||||
chr5:180353181 | G | A | 1 | a0001c0009t0001g0356 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7+30C>T | GFPT2 | ENSG00000131459.13 | transcript | ENST00000253778.13 | protein_coding | 1/18 | chr5 | 180353181 |