Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 132789 |
| ensemblid | ENSG00000163281.12 |
| hgncid | 21526 |
| symbol | GNPDA2 |
| name | glucosamine-6-phosphate deaminase 2 |
| refseq_nuc | NM_138335.3 |
| refseq_prot | NP_612208.1 |
| ensembl_nuc | ENST00000295448.8 |
| ensembl_prot | ENSP00000295448.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 44701795 |
| end | 44726556 |
| strand | - |
| ver | v1.2 |
| region | chr4:44701795-44726556 |
| region5000 | chr4:44696795-44731556 |
| regionname0 | GNPDA2_chr4_44701795_44726556 |
| regionname5000 | GNPDA2_chr4_44696795_44731556 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 828 | 405 | 96 | 74 | 196 | 9 | 30 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ATGAG others(823): Show |
chr4 | 44696795 | 44731556 | ||
| a0001c0002 | 0/0 | 828 | 5 | 0 | 2 | 0 | 1 | 2 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ATGAG others(823): Show |
chr4 | 44696795 | 44731556 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2235 | 144 | 29 | 36 | 60 | 5 | 14 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0002 | 0/0 | 2236 | 101 | 23 | 13 | 57 | 2 | 6 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2231): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0003 | 0/0 | 2235 | 76 | 16 | 10 | 41 | 1 | 8 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0004 | 0/0 | 2236 | 41 | 1 | 9 | 31 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2231): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0005 | 0/0 | 2231 | 8 | 6 | 2 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2226): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0006 | 0/0 | 2235 | 8 | 8 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0007 | 0/0 | 2236 | 5 | 0 | 0 | 5 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2231): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0008 | 0/0 | 2235 | 3 | 3 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0009 | 0/0 | 2235 | 3 | 0 | 2 | 0 | 0 | 1 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0010 | 0/0 | 2235 | 3 | 1 | 0 | 0 | 1 | 1 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0011 | 0/0 | 2235 | 2 | 0 | 0 | 2 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0012 | 0/0 | 2235 | 2 | 2 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0013 | 0/0 | 2235 | 2 | 2 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0014 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0015 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0016 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0017 | 0/0 | 2235 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0018 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0019 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2231): Show |
chr4 | 44696795 | 44731556 |
| a0001c0001t0020 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| a0001c0002t0003 | 0/0 | 2235 | 5 | 0 | 2 | 0 | 1 | 2 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | ACTGG others(2230): Show |
chr4 | 44696795 | 44731556 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 53 | 1 | 16 | 28 | 3 | 5 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0005 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0009 | 0/0 | 6 | 3 | 1 | 0 | 0 | 2 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 2 | 1 | 0 | 3 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0003 | 0/0 | 36 | 5 | 3 | 23 | 1 | 4 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0006 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0029 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0002 | 0/0 | 36 | 0 | 6 | 24 | 0 | 6 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0007 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0027 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0004 | 0/0 | 20 | 0 | 2 | 18 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0014 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0005g0012 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0006g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0007g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0009g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0010g0034 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0011g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0012g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0013g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0014g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0015g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0016g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0017g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0018g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0019g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| a0001c0002t0003g0013 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0045 | EUR | GBR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00642 | hp1 | a0001 | c0001 | t0009 | g0022 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01074 | hp2 | a0001 | c0001 | t0015 | g0069 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0013 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01168 | hp2 | a0001 | c0001 | t0009 | g0022 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0013 | AMR | PUR | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01261 | hp1 | a0001 | c0001 | t0017 | g0070 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0102 | EUR | IBS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0067 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | CDX | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CDX | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0050 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0150 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02572 | hp1 | a0001 | c0001 | t0018 | g0101 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0041 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02630 | hp2 | a0001 | c0001 | t0019 | g0140 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0138 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0046 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02970 | hp2 | a0001 | c0001 | t0013 | g0046 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0136 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0041 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0139 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03239 | hp1 | a0001 | c0001 | t0010 | g0034 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0013 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0013 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | ESN | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | BEB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG04199 | hp1 | a0001 | c0001 | t0009 | g0022 | SAS | STU | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | STU | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | STU | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | YRI | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | YRI | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18612 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | CHB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | CHB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | CHB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0153 | AFR | YRI | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18945 | hp2 | a0001 | c0001 | t0011 | g0031 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0126 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | LWK | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | LWK | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | LWK | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19063 | hp2 | a0001 | c0001 | t0011 | g0031 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19080 | hp1 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | YRI | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ASW | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0013 | EUR | TSI | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA20805 | hp1 | a0001 | c0001 | t0010 | g0034 | EUR | TSI | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0095 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| NA21309 | hp2 | a0001 | c0001 | t0020 | g0054 | AFR | LWK | GNPDA2_chr4_44696795_44731556 | GNPDA2 | chr4 | 44696795 | 44731556 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44703108 | T | C | 1 | a0001c0002 | 5 | HG01168.hp1 HG01243.hp2 HG03490.hp1 others(2): Show |
synonymous_variant | LOW | c.804A>G | p.Pro268Pro | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 922/2235 | 804/831 | 268/276 | chr4 | 44703108 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44702169 | CTTTA | C | 1 | a0001c0001t0005 | 8 | HG00639.hp2 HG01167.hp2 HG02451.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*908_*911delTAAA | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 908 | chr4 | 44702169 | ||||||
| chr4:44702189 | A | G | 7 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(4): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*892T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 892 | chr4 | 44702189 | ||||||
| chr4:44702242 | C | G | 1 | a0001c0001t0019 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 839 | chr4 | 44702242 | ||||||
| chr4:44702261 | A | T | 1 | a0001c0001t0007 | 5 | HG00558.hp2 NA18612.hp1 NA18959.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*820T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 820 | chr4 | 44702261 | ||||||
| chr4:44702298 | T | C | 1 | a0001c0001t0014 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 783 | chr4 | 44702298 | ||||||
| chr4:44702405 | A | G | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*676T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 676 | chr4 | 44702405 | ||||||
| chr4:44702406 | T | C | 2 | a0001c0001t0012 a0001c0001t0016 |
3 | HG02280.hp2 HG02622.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*675A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 675 | chr4 | 44702406 | ||||||
| chr4:44702418 | G | A | 3 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0013 |
12 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*663C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 663 | chr4 | 44702418 | ||||||
| chr4:44702498 | A | G | 1 | a0001c0001t0020 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*583T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 583 | chr4 | 44702498 | ||||||
| chr4:44702655 | G | C | 1 | a0001c0001t0013 | 2 | HG02965.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*426C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 426 | chr4 | 44702655 | ||||||
| chr4:44702672 | G | A | 1 | a0001c0001t0017 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*409C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 409 | chr4 | 44702672 | ||||||
| chr4:44702683 | A | G | 1 | a0001c0001t0010 | 3 | HG02055.hp1 HG03239.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*398T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 398 | chr4 | 44702683 | ||||||
| chr4:44702740 | C | T | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(14): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
3_prime_UTR_variant | MODIFIER | c.*341G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 341 | chr4 | 44702740 | ||||||
| chr4:44702773 | T | TG | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(1): Show |
148 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*307dupC | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 307 | chr4 | 44702773 | ||||||
| chr4:44702796 | G | A | 2 | a0001c0001t0006 a0001c0001t0013 |
10 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*285C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 285 | chr4 | 44702796 | ||||||
| chr4:44702824 | G | A | 1 | a0001c0001t0020 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*257C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 257 | chr4 | 44702824 | ||||||
| chr4:44702921 | T | A | 1 | a0001c0001t0004 | 41 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*160A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 7/7 | 160 | chr4 | 44702921 | ||||||
| chr4:44726497 | T | C | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(16): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
5_prime_UTR_variant | MODIFIER | c.-59A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/7 | 4290 | chr4 | 44726497 | ||||||
| chr4:44726513 | A | G | 1 | a0001c0001t0009 | 3 | HG00642.hp1 HG01168.hp2 HG04199.hp1 |
5_prime_UTR_variant | MODIFIER | c.-75T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/7 | 4306 | chr4 | 44726513 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:44703294 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.770-152T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44703294 | |||||||
| chr4:44703546 | G | C | 1 | a0001c0001t0006g0139 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.770-404C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44703546 | |||||||
| chr4:44703578 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(64): Show |
164 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.770-436C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44703578 | |||||||
| chr4:44703584 | T | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(56): Show |
154 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.770-442A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44703584 | |||||||
| chr4:44704310 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.770-1168T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44704310 | |||||||
| chr4:44704359 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(148): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.770-1217C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44704359 | |||||||
| chr4:44704375 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-1233T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44704375 | |||||||
| chr4:44704436 | T | C | 24 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0007 others(21): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.770-1294A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44704436 | |||||||
| chr4:44704537 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.770-1395A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44704537 | |||||||
| chr4:44704700 | A | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0113 |
5 | HG01993.hp1 HG02647.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.770-1558T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44704700 | |||||||
| chr4:44704740 | G | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0085 |
5 | NA18747.hp1 NA18970.hp1 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-1598C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44704740 | |||||||
| chr4:44704843 | T | C | 1 | a0001c0001t0002g0044 | 2 | HG02015.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.770-1701A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44704843 | |||||||
| chr4:44704902 | C | T | 21 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0017 others(18): Show |
80 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.770-1760G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44704902 | |||||||
| chr4:44704932 | C | T | 3 | a0001c0001t0005g0012 a0001c0001t0005g0152 a0001c0001t0005g0153 |
8 | HG00639.hp2 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.770-1790G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44704932 | |||||||
| chr4:44705036 | A | G | 63 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0008 others(60): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.770-1894T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705036 | |||||||
| chr4:44705170 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.770-2028C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705170 | |||||||
| chr4:44705256 | G | T | 1 | a0001c0001t0010g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.770-2114C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705256 | |||||||
| chr4:44705299 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.770-2157T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705299 | |||||||
| chr4:44705521 | A | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0068 others(3): Show |
12 | HG00733.hp2 HG01256.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.769+2231T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705521 | |||||||
| chr4:44705735 | A | G | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.769+2017T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705735 | |||||||
| chr4:44705757 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.769+1995A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705757 | |||||||
| chr4:44705798 | G | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.769+1954C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705798 | |||||||
| chr4:44705812 | G | A | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.769+1940C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705812 | |||||||
| chr4:44705861 | A | G | 1 | a0001c0001t0002g0047 | 2 | HG02056.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.769+1891T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705861 | |||||||
| chr4:44705922 | G | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.769+1830C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705922 | |||||||
| chr4:44705924 | C | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.769+1828G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44705924 | |||||||
| chr4:44706060 | A | G | 2 | a0001c0001t0003g0114 a0001c0001t0003g0115 |
2 | HG01255.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.769+1692T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706060 | |||||||
| chr4:44706069 | G | C | 23 | a0001c0001t0002g0025 a0001c0001t0003g0002 a0001c0001t0003g0007 others(20): Show |
84 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.769+1683C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706069 | |||||||
| chr4:44706076 | C | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(52): Show |
149 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.769+1676G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706076 | |||||||
| chr4:44706116 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.769+1636A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706116 | |||||||
| chr4:44706148 | A | T | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.769+1604T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706148 | |||||||
| chr4:44706232 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(147): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.769+1520C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706232 | |||||||
| chr4:44706260 | G | T | 1 | a0001c0001t0014g0050 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.769+1492C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706260 | |||||||
| chr4:44706308 | C | CTT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
156 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.769+1443_769+1444i others(4): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706308 | |||||||
| chr4:44706506 | A | G | 6 | a0001c0001t0006g0021 a0001c0001t0006g0095 a0001c0001t0006g0136 others(3): Show |
10 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.769+1246T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706506 | |||||||
| chr4:44706763 | T | A | 1 | a0001c0001t0001g0037 | 2 | NA18990.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.769+989A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706763 | |||||||
| chr4:44706789 | T | C | 32 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0029 others(29): Show |
79 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.769+963A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44706789 | |||||||
| chr4:44707304 | TA | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0014 a0001c0001t0004g0028 others(11): Show |
40 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.769+447delT | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44707304 | |||||||
| chr4:44707378 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.769+374C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44707378 | |||||||
| chr4:44707482 | A | G | 1 | a0001c0001t0003g0107 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.769+270T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44707482 | |||||||
| chr4:44707494 | T | A | 1 | a0001c0001t0001g0072 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.769+258A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44707494 | |||||||
| chr4:44707559 | GA | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(128): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.769+192delT | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44707559 | |||||||
| chr4:44707655 | T | C | 1 | a0001c0001t0006g0139 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+97A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44707655 | |||||||
| chr4:44707678 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(144): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.769+74G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44707678 | |||||||
| chr4:44707701 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0065 |
2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.769+51A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 6/6 | chr4 | 44707701 | |||||||
| chr4:44708080 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.595-154A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708080 | |||||||
| chr4:44708131 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.595-205T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708131 | |||||||
| chr4:44708329 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.595-403T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708329 | |||||||
| chr4:44708355 | A | G | 1 | a0001c0001t0014g0050 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.595-429T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708355 | |||||||
| chr4:44708433 | T | G | 2 | a0001c0001t0002g0008 a0001c0001t0002g0130 |
8 | HG00673.hp2 HG02129.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.595-507A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708433 | |||||||
| chr4:44708503 | GCACATAG others(15): Show |
G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.595-599_595-578del others(22): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708503 | |||||||
| chr4:44708627 | T | G | 1 | a0001c0001t0004g0137 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.595-701A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708627 | |||||||
| chr4:44708633 | T | C | 3 | a0001c0001t0003g0107 a0001c0001t0003g0108 a0001c0001t0003g0109 |
3 | HG02080.hp1 NA18984.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.595-707A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708633 | |||||||
| chr4:44708738 | TC | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0087 |
3 | HG01928.hp2 HG01975.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.595-813delG | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708738 | |||||||
| chr4:44708888 | CCAT | C | 2 | a0001c0001t0006g0136 a0001c0001t0013g0046 |
3 | HG02965.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.595-965_595-963del others(3): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708888 | |||||||
| chr4:44708956 | C | T | 1 | a0001c0001t0003g0106 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.595-1030G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44708956 | |||||||
| chr4:44709022 | A | G | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.595-1096T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709022 | |||||||
| chr4:44709160 | A | G | 1 | a0001c0001t0016g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.595-1234T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709160 | |||||||
| chr4:44709239 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.595-1313C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709239 | |||||||
| chr4:44709299 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.595-1373A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709299 | |||||||
| chr4:44709361 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0033 |
6 | HG02109.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-1435A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709361 | |||||||
| chr4:44709417 | G | A | 1 | a0001c0001t0012g0041 | 2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.595-1491C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709417 | |||||||
| chr4:44709444 | T | C | 2 | a0001c0001t0002g0097 a0001c0001t0002g0099 |
2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.594+1509A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709444 | |||||||
| chr4:44709446 | T | A | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.594+1507A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709446 | |||||||
| chr4:44709530 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
156 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.594+1423G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709530 | |||||||
| chr4:44709610 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.594+1343A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709610 | |||||||
| chr4:44709613 | A | C | 1 | a0001c0001t0002g0146 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.594+1340T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709613 | |||||||
| chr4:44709740 | A | ATGTAATT others(336): Show |
1 | a0001c0001t0014g0050 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.594+1212_594+1213i others(345): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709740 | |||||||
| chr4:44709754 | A | G | 1 | a0001c0001t0002g0042 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.594+1199T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709754 | |||||||
| chr4:44709800 | C | CA | 38 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0029 others(35): Show |
90 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.594+1152dupT | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709800 | |||||||
| chr4:44709800 | C | CAA | 3 | a0001c0001t0006g0021 a0001c0001t0006g0136 a0001c0001t0013g0046 |
7 | HG02145.hp1 HG02622.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.594+1151_594+1152d others(4): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709800 | |||||||
| chr4:44709800 | CA | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(59): Show |
157 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.594+1152delT | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709800 | |||||||
| chr4:44709886 | G | C | 2 | a0001c0001t0004g0117 a0001c0001t0004g0120 |
2 | NA18612.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.594+1067C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44709886 | |||||||
| chr4:44710120 | T | G | 1 | a0001c0001t0002g0141 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.594+833A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44710120 | |||||||
| chr4:44710131 | G | C | 3 | a0001c0001t0002g0030 a0001c0001t0002g0142 a0001c0001t0002g0148 |
5 | NA18948.hp2 NA18962.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+822C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44710131 | |||||||
| chr4:44710132 | T | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG02735.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.594+821A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44710132 | |||||||
| chr4:44710154 | T | G | 1 | a0001c0001t0004g0124 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.594+799A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44710154 | |||||||
| chr4:44710284 | T | G | 1 | a0001c0001t0002g0134 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.594+669A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44710284 | |||||||
| chr4:44710337 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.594+616T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44710337 | |||||||
| chr4:44710599 | T | C | 1 | a0001c0001t0003g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.594+354A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44710599 | |||||||
| chr4:44710710 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0068 others(3): Show |
12 | HG00733.hp2 HG01256.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.594+243A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44710710 | |||||||
| chr4:44710891 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
156 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.594+62A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 5/6 | chr4 | 44710891 | |||||||
| chr4:44711208 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.410-71C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711208 | |||||||
| chr4:44711218 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.410-81T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711218 | |||||||
| chr4:44711221 | AT | A | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.410-85delA | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711221 | |||||||
| chr4:44711221 | ATCACCTT others(1): Show |
A | 1 | a0001c0001t0001g0024 | 3 | HG00544.hp1 NA19009.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.410-92_410-85delCA others(6): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711221 | |||||||
| chr4:44711454 | T | C | 1 | a0001c0001t0002g0143 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.410-317A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711454 | |||||||
| chr4:44711672 | T | C | 1 | a0001c0001t0004g0121 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.410-535A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711672 | |||||||
| chr4:44711674 | G | A | 4 | a0001c0001t0006g0021 a0001c0001t0006g0095 a0001c0001t0006g0138 others(1): Show |
7 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.410-537C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711674 | |||||||
| chr4:44711688 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.410-551T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711688 | |||||||
| chr4:44711697 | T | C | 1 | a0001c0001t0002g0048 | 2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.410-560A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711697 | |||||||
| chr4:44711776 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.410-639G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711776 | |||||||
| chr4:44711809 | G | GTA | 11 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(8): Show |
15 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.410-674_410-673dup others(2): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711809 | |||||||
| chr4:44711809 | G | GTATA | 4 | a0001c0001t0003g0114 a0001c0001t0005g0012 a0001c0001t0005g0152 others(1): Show |
9 | HG00639.hp2 HG01167.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.410-676_410-673dup others(4): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711809 | |||||||
| chr4:44711809 | G | GTATATA | 13 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0026 others(10): Show |
61 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.410-678_410-673dup others(6): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711809 | |||||||
| chr4:44711809 | G | GTATATAT others(1): Show |
2 | a0001c0001t0003g0017 a0001c0001t0003g0019 |
8 | HG01891.hp2 HG02486.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.410-680_410-673dup others(8): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711809 | |||||||
| chr4:44711809 | G | GTATATAT others(3): Show |
2 | a0001c0001t0003g0110 a0001c0001t0003g0112 |
2 | HG03516.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.410-682_410-673dup others(10): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711809 | |||||||
| chr4:44711826 | T | C | 1 | a0001c0001t0002g0145 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.410-689A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711826 | |||||||
| chr4:44711826 | T | TAC | 26 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(23): Show |
53 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.410-690_410-689ins others(2): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711826 | |||||||
| chr4:44711828 | T | C | 79 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(76): Show |
196 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.410-691A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711828 | |||||||
| chr4:44711828 | T | TAC | 3 | a0001c0001t0002g0045 a0001c0001t0002g0144 a0001c0001t0004g0122 |
4 | HG00140.hp2 HG00558.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-693_410-692dup others(2): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711828 | |||||||
| chr4:44711828 | T | TACAC | 32 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0016 others(29): Show |
100 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.410-695_410-692dup others(4): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711828 | |||||||
| chr4:44711828 | T | TATATAC | 1 | a0001c0001t0003g0018 | 4 | HG02647.hp1 HG03209.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-692_410-691ins others(6): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711828 | |||||||
| chr4:44711865 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.410-728C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44711865 | |||||||
| chr4:44712255 | C | A | 1 | a0001c0001t0002g0146 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.410-1118G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44712255 | |||||||
| chr4:44712321 | A | G | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.410-1184T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44712321 | |||||||
| chr4:44712369 | A | C | 1 | a0001c0001t0004g0117 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.410-1232T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44712369 | |||||||
| chr4:44712413 | G | A | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.410-1276C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44712413 | |||||||
| chr4:44712438 | C | A | 15 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0047 others(12): Show |
55 | HG00099.hp1 HG00609.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.410-1301G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44712438 | |||||||
| chr4:44712520 | T | C | 1 | a0001c0001t0004g0123 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.410-1383A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44712520 | |||||||
| chr4:44712529 | TTATAAA | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.410-1398_410-1393d others(8): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44712529 | |||||||
| chr4:44712751 | G | A | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.410-1614C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44712751 | |||||||
| chr4:44713060 | C | T | 1 | a0001c0001t0002g0039 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.410-1923G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713060 | |||||||
| chr4:44713234 | G | C | 1 | a0001c0001t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.410-2097C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713234 | |||||||
| chr4:44713324 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(59): Show |
161 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.410-2187A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713324 | |||||||
| chr4:44713363 | T | C | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.410-2226A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713363 | |||||||
| chr4:44713386 | T | G | 1 | a0001c0001t0018g0101 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.410-2249A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713386 | |||||||
| chr4:44713783 | G | A | 17 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0029 others(14): Show |
37 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.410-2646C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713783 | |||||||
| chr4:44713805 | G | C | 1 | a0001c0001t0002g0042 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.410-2668C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713805 | |||||||
| chr4:44713824 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.410-2687T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713824 | |||||||
| chr4:44713833 | T | G | 1 | a0001c0001t0004g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.410-2696A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713833 | |||||||
| chr4:44713867 | G | A | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.410-2730C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713867 | |||||||
| chr4:44713911 | G | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(150): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.410-2774C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713911 | |||||||
| chr4:44713950 | G | T | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.410-2813C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713950 | |||||||
| chr4:44713993 | C | T | 3 | a0001c0001t0005g0012 a0001c0001t0005g0152 a0001c0001t0005g0153 |
8 | HG00639.hp2 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.410-2856G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44713993 | |||||||
| chr4:44714126 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.409+2987G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44714126 | |||||||
| chr4:44714197 | A | T | 1 | a0001c0001t0002g0127 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.409+2916T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44714197 | |||||||
| chr4:44714756 | T | A | 6 | a0001c0001t0006g0021 a0001c0001t0006g0095 a0001c0001t0006g0136 others(3): Show |
10 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.409+2357A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44714756 | |||||||
| chr4:44715001 | A | G | 3 | a0001c0001t0005g0012 a0001c0001t0005g0152 a0001c0001t0005g0153 |
8 | HG00639.hp2 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.409+2112T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44715001 | |||||||
| chr4:44715055 | T | C | 1 | a0001c0001t0008g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.409+2058A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44715055 | |||||||
| chr4:44715321 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(144): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.409+1792C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44715321 | |||||||
| chr4:44715675 | G | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0060 |
3 | HG01192.hp1 HG01255.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.409+1438C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44715675 | |||||||
| chr4:44715765 | A | C | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.409+1348T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44715765 | |||||||
| chr4:44715873 | T | C | 1 | a0001c0001t0002g0130 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.409+1240A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44715873 | |||||||
| chr4:44715893 | T | G | 16 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0029 others(13): Show |
36 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.409+1220A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44715893 | |||||||
| chr4:44716002 | T | A | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.409+1111A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716002 | |||||||
| chr4:44716150 | G | A | 13 | a0001c0001t0004g0004 a0001c0001t0004g0014 a0001c0001t0004g0028 others(10): Show |
39 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.409+963C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716150 | |||||||
| chr4:44716202 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(147): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.409+911A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716202 | |||||||
| chr4:44716203 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.409+910C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716203 | |||||||
| chr4:44716508 | T | C | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.409+605A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716508 | |||||||
| chr4:44716519 | T | TAC | 141 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(138): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.409+592_409+593dup others(2): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716519 | |||||||
| chr4:44716521 | C | CAT | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.409+591_409+592ins others(2): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716521 | |||||||
| chr4:44716622 | G | A | 1 | a0001c0001t0004g0124 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.409+491C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716622 | |||||||
| chr4:44716627 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.409+486C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716627 | |||||||
| chr4:44716866 | G | A | 1 | a0001c0001t0002g0131 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.409+247C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716866 | |||||||
| chr4:44716891 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.409+222G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716891 | |||||||
| chr4:44716991 | C | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(56): Show |
154 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.409+122G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44716991 | |||||||
| chr4:44717031 | A | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(56): Show |
154 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.409+82T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 4/6 | chr4 | 44717031 | |||||||
| chr4:44717366 | A | G | 1 | a0001c0001t0002g0096 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.227-71T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 3/6 | chr4 | 44717366 | |||||||
| chr4:44717504 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.227-209T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 3/6 | chr4 | 44717504 | |||||||
| chr4:44717810 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.226+499G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 3/6 | chr4 | 44717810 | |||||||
| chr4:44717876 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.226+433T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 3/6 | chr4 | 44717876 | |||||||
| chr4:44717943 | C | T | 1 | a0001c0001t0004g0118 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.226+366G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 3/6 | chr4 | 44717943 | |||||||
| chr4:44718134 | G | T | 1 | a0001c0001t0003g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.226+175C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 3/6 | chr4 | 44718134 | |||||||
| chr4:44718231 | T | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
156 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.226+78A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 3/6 | chr4 | 44718231 | |||||||
| chr4:44718450 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125-40A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718450 | |||||||
| chr4:44718614 | TG | T | 15 | a0001c0001t0002g0042 a0001c0001t0004g0004 a0001c0001t0004g0014 others(12): Show |
42 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.125-205delC | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718614 | |||||||
| chr4:44718617 | C | T | 15 | a0001c0001t0002g0042 a0001c0001t0004g0004 a0001c0001t0004g0014 others(12): Show |
42 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.125-207G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718617 | |||||||
| chr4:44718657 | G | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0082 |
8 | HG02027.hp2 NA18945.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-247C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718657 | |||||||
| chr4:44718717 | C | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
156 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.125-307G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718717 | |||||||
| chr4:44718750 | C | A | 2 | a0001c0001t0005g0152 a0001c0001t0005g0153 |
2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.125-340G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718750 | |||||||
| chr4:44718878 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(147): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.125-468G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718878 | |||||||
| chr4:44718941 | C | A | 1 | a0001c0001t0002g0135 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.125-531G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718941 | |||||||
| chr4:44718955 | A | G | 1 | a0001c0001t0002g0042 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.125-545T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718955 | |||||||
| chr4:44718956 | G | C | 1 | a0001c0001t0016g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-546C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718956 | |||||||
| chr4:44718963 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.125-553A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718963 | |||||||
| chr4:44718969 | A | C | 1 | a0001c0001t0004g0117 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.125-559T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44718969 | |||||||
| chr4:44719044 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
156 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.125-634G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44719044 | |||||||
| chr4:44719086 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
156 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.125-676G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44719086 | |||||||
| chr4:44719161 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.125-751A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44719161 | |||||||
| chr4:44719237 | G | A | 1 | a0001c0001t0002g0042 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.125-827C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44719237 | |||||||
| chr4:44719277 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.125-867G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44719277 | |||||||
| chr4:44719756 | T | C | 1 | a0001c0001t0001g0038 | 2 | HG01123.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.125-1346A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44719756 | |||||||
| chr4:44719772 | G | C | 1 | a0001c0001t0001g0083 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.125-1362C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44719772 | |||||||
| chr4:44719922 | A | C | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.125-1512T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44719922 | |||||||
| chr4:44720115 | A | G | 1 | a0001c0001t0003g0104 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.125-1705T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44720115 | |||||||
| chr4:44720117 | C | G | 1 | a0001c0001t0016g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-1707G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44720117 | |||||||
| chr4:44720395 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.124+1689C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44720395 | |||||||
| chr4:44720397 | G | GAAAGC | 3 | a0001c0001t0005g0012 a0001c0001t0005g0152 a0001c0001t0005g0153 |
8 | HG00639.hp2 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.124+1682_124+1686d others(7): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44720397 | |||||||
| chr4:44720565 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.124+1519G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44720565 | |||||||
| chr4:44720626 | T | C | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.124+1458A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44720626 | |||||||
| chr4:44720719 | A | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
6 | HG00642.hp2 HG01123.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+1365T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44720719 | |||||||
| chr4:44721006 | T | C | 2 | a0001c0001t0004g0028 a0001c0001t0004g0116 |
4 | NA18969.hp2 NA18975.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+1078A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721006 | |||||||
| chr4:44721056 | GA | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(54): Show |
152 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.124+1027delT | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721056 | |||||||
| chr4:44721057 | A | G | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.124+1027T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721057 | |||||||
| chr4:44721058 | A | G | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.124+1026T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721058 | |||||||
| chr4:44721207 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
156 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.124+877G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721207 | |||||||
| chr4:44721229 | G | A | 1 | a0001c0001t0005g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.124+855C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721229 | |||||||
| chr4:44721316 | G | C | 1 | a0001c0001t0004g0125 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.124+768C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721316 | |||||||
| chr4:44721410 | T | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.124+674A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721410 | |||||||
| chr4:44721474 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.124+610G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721474 | |||||||
| chr4:44721602 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.124+482T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721602 | |||||||
| chr4:44721629 | TTATATAA | T | 22 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0017 others(19): Show |
81 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.124+448_124+454del others(7): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721629 | |||||||
| chr4:44721662 | A | C | 1 | a0001c0001t0003g0026 | 3 | HG02071.hp2 HG02080.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.124+422T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721662 | |||||||
| chr4:44721712 | C | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+372G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721712 | |||||||
| chr4:44721714 | T | A | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+370A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721714 | |||||||
| chr4:44721715 | T | A | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+369A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721715 | |||||||
| chr4:44721717 | G | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+367C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721717 | |||||||
| chr4:44721728 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+356T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721728 | |||||||
| chr4:44721729 | T | A | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+355A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721729 | |||||||
| chr4:44721730 | G | A | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+354C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721730 | |||||||
| chr4:44721731 | A | G | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+353T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721731 | |||||||
| chr4:44721733 | T | G | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+351A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721733 | |||||||
| chr4:44721734 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+350T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721734 | |||||||
| chr4:44721739 | G | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+345C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721739 | |||||||
| chr4:44721741 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+343T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721741 | |||||||
| chr4:44721743 | G | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+341C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721743 | |||||||
| chr4:44721750 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+334T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721750 | |||||||
| chr4:44721753 | T | A | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+331A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721753 | |||||||
| chr4:44721754 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+330T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721754 | |||||||
| chr4:44721755 | A | G | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+329T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721755 | |||||||
| chr4:44721758 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+326T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721758 | |||||||
| chr4:44721761 | G | A | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+323C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721761 | |||||||
| chr4:44721763 | T | G | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+321A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721763 | |||||||
| chr4:44721765 | T | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+319A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721765 | |||||||
| chr4:44721766 | G | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+318C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721766 | |||||||
| chr4:44721768 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+316T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721768 | |||||||
| chr4:44721773 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+311T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721773 | |||||||
| chr4:44721775 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+309T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721775 | |||||||
| chr4:44721776 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+308T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721776 | |||||||
| chr4:44721777 | G | A | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+307C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721777 | |||||||
| chr4:44721779 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+305T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721779 | |||||||
| chr4:44721781 | T | A | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+303A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721781 | |||||||
| chr4:44721782 | G | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+302C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721782 | |||||||
| chr4:44721789 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+295T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721789 | |||||||
| chr4:44721790 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+294T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721790 | |||||||
| chr4:44721791 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+293T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721791 | |||||||
| chr4:44721799 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+285T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721799 | |||||||
| chr4:44721803 | C | G | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+281G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721803 | |||||||
| chr4:44721805 | A | G | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+279T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721805 | |||||||
| chr4:44721808 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+276T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721808 | |||||||
| chr4:44721809 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+275T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721809 | |||||||
| chr4:44721810 | A | G | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+274T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721810 | |||||||
| chr4:44721811 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+273T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721811 | |||||||
| chr4:44721815 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+269T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721815 | |||||||
| chr4:44721816 | C | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+268G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721816 | |||||||
| chr4:44721818 | A | G | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+266T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721818 | |||||||
| chr4:44721821 | A | C | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+263T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721821 | |||||||
| chr4:44721829 | C | A | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+255G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721829 | |||||||
| chr4:44721832 | C | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+252G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721832 | |||||||
| chr4:44721833 | A | G | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+251T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721833 | |||||||
| chr4:44721837 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+247T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721837 | |||||||
| chr4:44721838 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+246T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721838 | |||||||
| chr4:44721842 | A | T | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+242T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721842 | |||||||
| chr4:44721850 | T | A | 1 | a0001c0001t0003g0111 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+234A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721850 | |||||||
| chr4:44721971 | T | C | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.124+113A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 2/6 | chr4 | 44721971 | |||||||
| chr4:44722332 | C | A | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-35-90G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722332 | |||||||
| chr4:44722444 | C | G | 1 | a0001c0001t0002g0127 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-35-202G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722444 | |||||||
| chr4:44722469 | C | A | 6 | a0001c0001t0002g0029 a0001c0001t0002g0133 a0001c0001t0002g0134 others(3): Show |
11 | HG00558.hp2 HG01496.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-227G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722469 | |||||||
| chr4:44722516 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(147): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.-35-274C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722516 | |||||||
| chr4:44722549 | A | G | 15 | a0001c0001t0003g0002 a0001c0001t0003g0017 a0001c0001t0003g0026 others(12): Show |
62 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.-35-307T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722549 | |||||||
| chr4:44722553 | G | A | 2 | a0001c0001t0006g0136 a0001c0001t0013g0046 |
3 | HG02965.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-35-311C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722553 | |||||||
| chr4:44722632 | A | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
6 | HG00642.hp2 HG01123.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35-390T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722632 | |||||||
| chr4:44722656 | A | G | 1 | a0001c0001t0003g0102 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-35-414T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722656 | |||||||
| chr4:44722704 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-35-462A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722704 | |||||||
| chr4:44722773 | T | G | 1 | a0001c0001t0004g0043 | 2 | HG00735.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-35-531A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722773 | |||||||
| chr4:44722883 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-35-641A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722883 | |||||||
| chr4:44722939 | C | T | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-35-697G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44722939 | |||||||
| chr4:44723153 | C | T | 1 | a0001c0001t0007g0126 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-35-911G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723153 | |||||||
| chr4:44723204 | C | T | 15 | a0001c0001t0002g0042 a0001c0001t0004g0004 a0001c0001t0004g0014 others(12): Show |
42 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-35-962G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723204 | |||||||
| chr4:44723255 | T | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(64): Show |
168 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.-35-1013A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723255 | |||||||
| chr4:44723302 | T | C | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-35-1060A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723302 | |||||||
| chr4:44723317 | G | C | 23 | a0001c0001t0003g0002 a0001c0001t0003g0007 a0001c0001t0003g0017 others(20): Show |
82 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-35-1075C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723317 | |||||||
| chr4:44723325 | G | T | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-35-1083C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723325 | |||||||
| chr4:44723382 | T | G | 16 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0047 others(13): Show |
56 | HG00099.hp1 HG00609.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-35-1140A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723382 | |||||||
| chr4:44723447 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1205G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723447 | |||||||
| chr4:44723448 | C | A | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1206G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723448 | |||||||
| chr4:44723450 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1208G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723450 | |||||||
| chr4:44723459 | A | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1217T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723459 | |||||||
| chr4:44723461 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1219A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723461 | |||||||
| chr4:44723464 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1222A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723464 | |||||||
| chr4:44723465 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1223A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723465 | |||||||
| chr4:44723476 | T | A | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1234A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723476 | |||||||
| chr4:44723480 | A | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1238T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723480 | |||||||
| chr4:44723481 | G | A | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1239C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723481 | |||||||
| chr4:44723487 | A | T | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1245T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723487 | |||||||
| chr4:44723492 | T | A | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1250A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723492 | |||||||
| chr4:44723500 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1258A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723500 | |||||||
| chr4:44723501 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1259A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723501 | |||||||
| chr4:44723505 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1263A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723505 | |||||||
| chr4:44723506 | C | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1264G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723506 | |||||||
| chr4:44723507 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1265A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723507 | |||||||
| chr4:44723509 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1267A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723509 | |||||||
| chr4:44723512 | G | T | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1270C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723512 | |||||||
| chr4:44723520 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1278A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723520 | |||||||
| chr4:44723521 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1279A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723521 | |||||||
| chr4:44723537 | G | C | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1295C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723537 | |||||||
| chr4:44723540 | T | G | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1298A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723540 | |||||||
| chr4:44723552 | A | T | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1310T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723552 | |||||||
| chr4:44723571 | T | A | 1 | a0001c0001t0002g0148 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-35-1329A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723571 | |||||||
| chr4:44723586 | C | T | 1 | a0001c0001t0011g0031 | 2 | NA18945.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-35-1344G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723586 | |||||||
| chr4:44723589 | G | A | 1 | a0001c0001t0020g0054 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-35-1347C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723589 | |||||||
| chr4:44723767 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.-35-1525C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723767 | |||||||
| chr4:44723881 | C | T | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-35-1639G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723881 | |||||||
| chr4:44723894 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
6 | HG00642.hp2 HG01123.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35-1652G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44723894 | |||||||
| chr4:44724064 | G | T | 15 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0047 others(12): Show |
55 | HG00099.hp1 HG00609.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.-35-1822C>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724064 | |||||||
| chr4:44724248 | A | T | 1 | a0001c0001t0001g0055 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-35-2006T>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724248 | |||||||
| chr4:44724438 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-36+2036A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724438 | |||||||
| chr4:44724475 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-36+1999C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724475 | |||||||
| chr4:44724477 | A | C | 1 | a0001c0001t0016g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-36+1997T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724477 | |||||||
| chr4:44724579 | A | AT | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.-36+1894dupA | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724579 | |||||||
| chr4:44724654 | T | C | 16 | a0001c0001t0002g0003 a0001c0001t0002g0030 a0001c0001t0002g0047 others(13): Show |
56 | HG00099.hp1 HG00609.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.-36+1820A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724654 | |||||||
| chr4:44724660 | T | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
6 | HG00642.hp2 HG01123.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36+1814A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724660 | |||||||
| chr4:44724662 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-36+1812C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724662 | |||||||
| chr4:44724733 | T | A | 1 | a0001c0001t0001g0089 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-36+1741A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724733 | |||||||
| chr4:44724780 | A | G | 1 | a0001c0002t0003g0013 | 5 | HG01168.hp1 HG01243.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36+1694T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44724780 | |||||||
| chr4:44725101 | T | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.-36+1373A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725101 | |||||||
| chr4:44725134 | CTATTA | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.-36+1335_-36+1339d others(7): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725134 | |||||||
| chr4:44725211 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(51): Show |
148 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.-36+1263G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725211 | |||||||
| chr4:44725391 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.-36+1083C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725391 | |||||||
| chr4:44725493 | A | C | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36+981T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725493 | |||||||
| chr4:44725580 | C | T | 3 | a0001c0001t0005g0012 a0001c0001t0005g0152 a0001c0001t0005g0153 |
8 | HG00639.hp2 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-36+894G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725580 | |||||||
| chr4:44725614 | CAG | C | 1 | a0001c0001t0001g0005 | 11 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-36+858_-36+859del others(2): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725614 | |||||||
| chr4:44725646 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-36+828G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725646 | |||||||
| chr4:44725710 | T | C | 1 | a0001c0001t0016g0150 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-36+764A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725710 | |||||||
| chr4:44725743 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
156 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.-36+731G>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725743 | |||||||
| chr4:44725766 | C | CACG | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(81): Show |
238 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.-36+707_-36+708ins others(3): Show |
GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725766 | |||||||
| chr4:44725878 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0151 |
3 | HG02040.hp1 HG02040.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-36+596C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725878 | |||||||
| chr4:44725892 | G | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(147): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.-36+582C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725892 | |||||||
| chr4:44725923 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-36+551G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725923 | |||||||
| chr4:44725971 | C | A | 3 | a0001c0001t0005g0012 a0001c0001t0005g0152 a0001c0001t0005g0153 |
8 | HG00639.hp2 HG01167.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-36+503G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44725971 | |||||||
| chr4:44726147 | A | G | 9 | a0001c0001t0002g0025 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
13 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36+327T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726147 | |||||||
| chr4:44726262 | C | T | 1 | a0001c0001t0006g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-36+212G>A | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726262 | |||||||
| chr4:44726314 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-36+160C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726314 | |||||||
| chr4:44726344 | T | G | 1 | a0001c0001t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-36+130A>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726344 | |||||||
| chr4:44726383 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+91C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726383 | |||||||
| chr4:44726385 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+89T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726385 | |||||||
| chr4:44726387 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+87T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726387 | |||||||
| chr4:44726391 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+83C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726391 | |||||||
| chr4:44726394 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+80C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726394 | |||||||
| chr4:44726396 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+78T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726396 | |||||||
| chr4:44726399 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+75C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726399 | |||||||
| chr4:44726400 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+74C>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726400 | |||||||
| chr4:44726401 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+73C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726401 | |||||||
| chr4:44726403 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+71C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726403 | |||||||
| chr4:44726404 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+70T>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726404 | |||||||
| chr4:44726406 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+68C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726406 | |||||||
| chr4:44726407 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+67A>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726407 | |||||||
| chr4:44726408 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+66A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726408 | |||||||
| chr4:44726409 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+65C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726409 | |||||||
| chr4:44726413 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+61A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726413 | |||||||
| chr4:44726417 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+57C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726417 | |||||||
| chr4:44726424 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+50C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726424 | |||||||
| chr4:44726425 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(57): Show |
155 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.-36+49T>C | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726425 | |||||||
| chr4:44726432 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+42A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726432 | |||||||
| chr4:44726437 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+37A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726437 | |||||||
| chr4:44726438 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+36A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726438 | |||||||
| chr4:44726440 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+34A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726440 | |||||||
| chr4:44726441 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+33A>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726441 | |||||||
| chr4:44726442 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+32C>G | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726442 | |||||||
| chr4:44726446 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-36+28G>T | GNPDA2 | ENSG00000163281.12 | transcript | ENST00000295448.8 | protein_coding | 1/6 | chr4 | 44726446 |