Item | Value |
---|---|
geneid | 84803 |
ensemblid | ENSG00000138678.11 |
hgncid | 28157 |
symbol | GPAT3 |
name | glycerol-3-phosphate acyltransferase 3 |
refseq_nuc | NM_032717.5 |
refseq_prot | NP_116106.2 |
ensembl_nuc | ENST00000264409.5 |
ensembl_prot | ENSP00000264409.4 |
mane_status | MANE Select |
chr | chr4 |
start | 83536108 |
end | 83605875 |
strand | + |
ver | v1.2 |
region | chr4:83536108-83605875 |
region5000 | chr4:83531108-83610875 |
regionname0 | GPAT3_chr4_83536108_83605875 |
regionname5000 | GPAT3_chr4_83531108_83610875 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 434 | 327 | 92 | 45 | 140 | 11 | 37 | 116 | GPAT3_chr4_83531108_83610875 | GPAT3 | MEGAE others(429): Show |
chr4 | 83531108 | 83610875 |
a0002 | 0/0 | 434 | 5 | 0 | 3 | 0 | 1 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | MEGAE others(429): Show |
chr4 | 83531108 | 83610875 |
a0003 | 0/0 | 434 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | MEGAE others(429): Show |
chr4 | 83531108 | 83610875 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1302 | 326 | 91 | 45 | 140 | 11 | 37 | GPAT3_chr4_83531108_83610875 | GPAT3 | ATGGA others(1297): Show |
chr4 | 83531108 | 83610875 | ||
a0001c0004 | 0/0 | 1302 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | ATGGA others(1297): Show |
chr4 | 83531108 | 83610875 | ||
a0002c0002 | 0/0 | 1302 | 5 | 0 | 3 | 0 | 1 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | ATGGA others(1297): Show |
chr4 | 83531108 | 83610875 | ||
a0003c0003 | 0/0 | 1302 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | ATGGA others(1297): Show |
chr4 | 83531108 | 83610875 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2928 | 107 | 14 | 15 | 60 | 2 | 14 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0002 | 0/0 | 2928 | 95 | 29 | 10 | 46 | 4 | 6 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0003 | 0/0 | 2928 | 70 | 5 | 15 | 30 | 4 | 16 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0004 | 0/0 | 2928 | 18 | 15 | 3 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0005 | 0/0 | 2928 | 17 | 16 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0006 | 0/0 | 2928 | 4 | 4 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0007 | 0/0 | 2928 | 3 | 3 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0008 | 0/0 | 2925 | 3 | 0 | 0 | 3 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2920): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0009 | 0/0 | 2928 | 2 | 2 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0010 | 0/0 | 2928 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0011 | 0/0 | 2927 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2922): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0012 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0013 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0014 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0001t0015 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0001c0004t0004 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0002c0002t0003 | 0/0 | 2928 | 5 | 0 | 3 | 0 | 1 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
a0003c0003t0002 | 0/0 | 2928 | 2 | 0 | 2 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | AGCTT others(2923): Show |
chr4 | 83531108 | 83610875 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0100 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0007g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0007g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0008g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0008g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0009g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0009g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0010g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0010g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0011g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0012g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0013g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0014g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0001t0015g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0001c0004t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0002c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0002c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0002c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0002c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0002c0002t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0003c0003t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
a0003c0003t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0205 | EUR | GBR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0266 | EUR | GBR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0292 | EUR | GBR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | GBR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0191 | EUR | FIN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0218 | EUR | FIN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0327 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01192 | hp2 | a0002 | c0002 | t0003 | g0290 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0306 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01256 | hp2 | a0001 | c0001 | t0010 | g0267 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01257 | hp2 | a0002 | c0002 | t0003 | g0145 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01258 | hp2 | a0002 | c0002 | t0003 | g0146 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0115 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01433 | hp2 | a0001 | c0001 | t0010 | g0244 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0291 | EUR | IBS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0253 | EUR | IBS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG01993 | hp2 | a0003 | c0003 | t0002 | g0284 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0314 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02055 | hp1 | a0001 | c0001 | t0015 | g0180 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | CDX | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02300 | hp1 | a0003 | c0003 | t0002 | g0283 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PEL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0212 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02622 | hp2 | a0001 | c0001 | t0007 | g0189 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0221 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0296 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0330 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02735 | hp1 | a0001 | c0001 | t0011 | g0274 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0181 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0333 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03041 | hp2 | a0001 | c0001 | t0012 | g0243 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0187 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03139 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0188 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0245 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0288 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0211 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0182 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03579 | hp2 | a0001 | c0004 | t0004 | g0305 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0293 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0137 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0175 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0301 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0321 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | BEB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0326 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | STU | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0318 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | CHB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0186 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18948 | hp1 | a0001 | c0001 | t0008 | g0075 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18956 | hp1 | a0001 | c0001 | t0008 | g0102 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18988 | hp1 | a0001 | c0001 | t0013 | g0171 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18991 | hp2 | a0001 | c0001 | t0008 | g0174 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0311 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0184 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0331 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | YRI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ASW | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | ASW | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0303 | EUR | TSI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0289 | EUR | TSI | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | GIH | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA20905 | hp2 | a0002 | c0002 | t0003 | g0248 | SAS | GIH | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0309 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | MSL | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | USA | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | USA | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | USA | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0190 | AFR | USA | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0196 | AFR | LWK | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0160 | REF | REF | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0100 | REF | REF | GPAT3_chr4_83531108_83610875 | GPAT3 | chr4 | 83531108 | 83610875 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83544578 | A | G | 1 | a0003 | 2 | HG01993.hp2 HG02300.hp1 |
missense_variant | MODERATE | c.184A>G | p.Ile62Val | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/12 | 699/2928 | 184/1305 | 62/434 | chr4 | 83544578 | |||
chr4:83598675 | G | A | 1 | a0002 | 5 | HG01192.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
missense_variant | MODERATE | c.1157G>A | p.Arg386Lys | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/12 | 1672/2928 | 1157/1305 | 386/434 | chr4 | 83598675 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83594850 | C | G | 1 | a0001c0004 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.744C>G | p.Gly248Gly | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/12 | 1259/2928 | 744/1305 | 248/434 | chr4 | 83594850 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83536131 | C | G | 2 | a0001c0001t0014 a0001c0001t0015 |
2 | HG02055.hp1 HG02809.hp1 |
5_prime_UTR_variant | MODIFIER | c.-492C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/12 | 492 | chr4 | 83536131 | ||||||
chr4:83536133 | G | C | 2 | a0001c0001t0007 a0001c0001t0009 |
5 | HG02622.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-490G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/12 | chr4 | 83536133 | |||||||
chr4:83536203 | C | G | 1 | a0001c0001t0009 | 2 | HG03130.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-420C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/12 | 420 | chr4 | 83536203 | ||||||
chr4:83536412 | TTAA | T | 1 | a0001c0001t0008 | 3 | NA18948.hp1 NA18956.hp1 NA18991.hp2 |
5_prime_UTR_variant | MODIFIER | c.-210_-208delTAA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/12 | 208 | chr4 | 83536412 | ||||||
chr4:83536416 | C | G | 1 | a0001c0001t0008 | 3 | NA18948.hp1 NA18956.hp1 NA18991.hp2 |
5_prime_UTR_variant | MODIFIER | c.-207C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/12 | 207 | chr4 | 83536416 | ||||||
chr4:83604820 | CT | C | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(4): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*60delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 60 | INFO_REALIGN_3_PRIME | chr4 | 83604820 | |||||
chr4:83604860 | A | G | 1 | a0001c0001t0010 | 2 | HG01256.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*93A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 93 | chr4 | 83604860 | ||||||
chr4:83605122 | T | C | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(9): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*355T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 355 | chr4 | 83605122 | ||||||
chr4:83605348 | C | T | 1 | a0001c0001t0013 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 581 | chr4 | 83605348 | ||||||
chr4:83605383 | C | T | 2 | a0001c0001t0003 a0002c0002t0003 |
75 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*616C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 616 | chr4 | 83605383 | ||||||
chr4:83605420 | A | G | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(11): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*653A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 653 | chr4 | 83605420 | ||||||
chr4:83605547 | T | TA | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(3): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*792dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 793 | INFO_REALIGN_3_PRIME | chr4 | 83605547 | |||||
chr4:83605614 | C | T | 5 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(2): Show |
103 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*847C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 847 | chr4 | 83605614 | ||||||
chr4:83605707 | A | C | 1 | a0001c0001t0006 | 4 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*940A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 940 | chr4 | 83605707 | ||||||
chr4:83605844 | T | G | 1 | a0001c0001t0012 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1077T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 12/12 | 1077 | chr4 | 83605844 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:83536848 | A | G | 97 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(94): Show |
97 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.141+85A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83536848 | |||||||
chr4:83536875 | C | G | 97 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(94): Show |
97 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.141+112C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83536875 | |||||||
chr4:83536880 | G | A | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.141+117G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83536880 | |||||||
chr4:83536940 | G | T | 1 | a0001c0001t0001g0236 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.141+177G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83536940 | |||||||
chr4:83537228 | C | G | 9 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(6): Show |
9 | HG02258.hp2 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+465C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537228 | |||||||
chr4:83537348 | C | G | 31 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0208 others(28): Show |
31 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.141+585C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537348 | |||||||
chr4:83537563 | TA | T | 9 | a0001c0001t0003g0197 a0001c0001t0004g0199 a0001c0001t0004g0200 others(6): Show |
9 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.141+809delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537563 | ||||||
chr4:83537564 | A | T | 13 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0208 others(10): Show |
13 | HG02027.hp2 HG02145.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.141+801A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537564 | |||||||
chr4:83537589 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0005g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.141+827_141+828ins others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537589 | ||||||
chr4:83537591 | A | ATG | 34 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0050 others(31): Show |
34 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.141+862_141+863dup others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | ||||||
chr4:83537591 | A | ATGTG | 4 | a0001c0001t0001g0124 a0001c0001t0001g0176 a0001c0001t0002g0330 others(1): Show |
4 | HG01175.hp2 HG02717.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+860_141+863dup others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | ||||||
chr4:83537591 | A | ATGTGTG | 5 | a0001c0001t0001g0008 a0001c0001t0003g0006 a0001c0001t0003g0015 others(2): Show |
5 | HG00642.hp1 HG00741.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+858_141+863dup others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | ||||||
chr4:83537591 | A | ATGTGTGT others(1): Show |
10 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(7): Show |
10 | HG00733.hp2 HG02486.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+856_141+863dup others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | ||||||
chr4:83537591 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0005g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.141+854_141+863dup others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | ||||||
chr4:83537591 | A | G | 36 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0208 others(33): Show |
36 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.141+828A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537591 | |||||||
chr4:83537591 | ATG | A | 21 | a0001c0001t0002g0024 a0001c0001t0002g0049 a0001c0001t0003g0001 others(18): Show |
21 | HG00438.hp2 HG00597.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.141+862_141+863del others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | ||||||
chr4:83537591 | ATGTG | A | 5 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0046 others(2): Show |
5 | HG02258.hp1 NA18612.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+860_141+863del others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | ||||||
chr4:83537591 | ATGTGTG | A | 9 | a0001c0001t0005g0182 a0001c0001t0005g0184 a0001c0001t0007g0188 others(6): Show |
9 | HG02055.hp1 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+858_141+863del others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537591 | ||||||
chr4:83537593 | G | A | 1 | a0001c0001t0002g0328 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.141+830G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537593 | |||||||
chr4:83537621 | G | GTA | 6 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(3): Show |
6 | HG02896.hp1 HG02897.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+859_141+860ins others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537621 | ||||||
chr4:83537623 | G | A | 7 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(4): Show |
7 | HG02896.hp1 HG02897.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+860G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537623 | |||||||
chr4:83537623 | G | GTA | 83 | a0001c0001t0001g0254 a0001c0001t0001g0297 a0001c0001t0001g0300 others(80): Show |
83 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.141+861_141+862ins others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537623 | ||||||
chr4:83537625 | G | A | 115 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.141+862G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537625 | |||||||
chr4:83537625 | G | GTA | 3 | a0001c0001t0002g0222 a0001c0001t0002g0235 a0001c0001t0002g0329 |
3 | HG03041.hp1 NA19006.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.141+866_141+867dup others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537625 | ||||||
chr4:83537625 | G | GTATA | 3 | a0001c0001t0002g0328 a0001c0001t0003g0326 a0001c0001t0003g0327 |
3 | HG01169.hp2 HG04228.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.141+864_141+867dup others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537625 | ||||||
chr4:83537625 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0003g0194 a0001c0001t0004g0195 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.141+863_141+864ins others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83537625 | ||||||
chr4:83537627 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0002g0192 a0001c0001t0003g0191 |
3 | HG00280.hp1 HG02970.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.141+864A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537627 | |||||||
chr4:83537706 | G | C | 1 | a0001c0001t0002g0222 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.141+943G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537706 | |||||||
chr4:83537733 | G | T | 1 | a0001c0001t0002g0328 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.141+970G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537733 | |||||||
chr4:83537746 | C | T | 2 | a0001c0001t0002g0332 a0001c0001t0005g0331 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.141+983C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537746 | |||||||
chr4:83537784 | C | T | 5 | a0001c0001t0007g0188 a0001c0001t0007g0189 a0001c0001t0007g0190 others(2): Show |
5 | HG02622.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+1021C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537784 | |||||||
chr4:83537805 | T | A | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.141+1042T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537805 | |||||||
chr4:83537817 | G | A | 1 | a0001c0001t0012g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.141+1054G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537817 | |||||||
chr4:83537848 | T | C | 2 | a0001c0001t0002g0332 a0001c0001t0005g0331 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.141+1085T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83537848 | |||||||
chr4:83538095 | A | T | 1 | a0001c0001t0003g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.141+1332A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538095 | |||||||
chr4:83538365 | A | G | 5 | a0001c0001t0003g0183 a0001c0001t0005g0182 a0001c0001t0005g0184 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+1602A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538365 | |||||||
chr4:83538479 | C | T | 1 | a0001c0001t0002g0325 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.141+1716C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538479 | |||||||
chr4:83538562 | G | A | 3 | a0001c0001t0005g0205 a0001c0001t0014g0181 a0001c0001t0015g0180 |
3 | HG00099.hp1 HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.141+1799G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538562 | |||||||
chr4:83538689 | A | G | 1 | a0001c0001t0002g0324 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.141+1926A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538689 | |||||||
chr4:83538713 | C | A | 2 | a0001c0001t0002g0332 a0001c0001t0005g0331 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.141+1950C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538713 | |||||||
chr4:83538713 | C | G | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.141+1950C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538713 | |||||||
chr4:83538797 | A | C | 97 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(94): Show |
97 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.141+2034A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538797 | |||||||
chr4:83538804 | T | G | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.141+2041T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538804 | |||||||
chr4:83538864 | A | C | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.141+2101A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538864 | |||||||
chr4:83538942 | A | T | 9 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(6): Show |
9 | HG02258.hp2 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+2179A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83538942 | |||||||
chr4:83539018 | T | C | 2 | a0001c0001t0003g0194 a0001c0001t0004g0195 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.141+2255T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539018 | |||||||
chr4:83539041 | A | G | 97 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(94): Show |
97 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.141+2278A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539041 | |||||||
chr4:83539060 | G | A | 2 | a0001c0001t0002g0332 a0001c0001t0005g0331 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.141+2297G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539060 | |||||||
chr4:83539268 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0006g0206 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.141+2505G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539268 | |||||||
chr4:83539350 | C | A | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.141+2587C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539350 | |||||||
chr4:83539381 | C | T | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.141+2618C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539381 | |||||||
chr4:83539820 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.141+3057C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539820 | |||||||
chr4:83539924 | G | A | 41 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0208 others(38): Show |
41 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.141+3161G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539924 | |||||||
chr4:83539924 | G | C | 1 | a0001c0001t0003g0005 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.141+3161G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539924 | |||||||
chr4:83539947 | T | C | 162 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0217 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.141+3184T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539947 | |||||||
chr4:83539962 | G | A | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.141+3199G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83539962 | |||||||
chr4:83540112 | A | G | 94 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.141+3349A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540112 | |||||||
chr4:83540155 | T | TA | 16 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(13): Show |
16 | HG00438.hp2 HG00741.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.141+3414dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83540155 | ||||||
chr4:83540155 | TA | T | 7 | a0001c0001t0001g0178 a0001c0001t0002g0323 a0001c0001t0002g0330 others(4): Show |
7 | HG01891.hp1 HG02717.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+3414delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83540155 | ||||||
chr4:83540155 | TAA | T | 33 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0208 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.141+3413_141+3414d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83540155 | ||||||
chr4:83540310 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.141+3547G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540310 | |||||||
chr4:83540354 | C | T | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.141+3591C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540354 | |||||||
chr4:83540550 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.141+3787C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540550 | |||||||
chr4:83540560 | G | A | 1 | a0001c0001t0002g0029 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.141+3797G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540560 | |||||||
chr4:83540627 | C | T | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.141+3864C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540627 | |||||||
chr4:83540722 | G | C | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.142-3814G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540722 | |||||||
chr4:83540761 | C | T | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-3775C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540761 | |||||||
chr4:83540857 | T | C | 94 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.142-3679T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540857 | |||||||
chr4:83540974 | A | G | 136 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.142-3562A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540974 | |||||||
chr4:83540981 | T | C | 162 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0217 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.142-3555T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540981 | |||||||
chr4:83540989 | T | C | 94 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.142-3547T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83540989 | |||||||
chr4:83541087 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.142-3449C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541087 | |||||||
chr4:83541175 | A | G | 94 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.142-3361A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541175 | |||||||
chr4:83541246 | T | G | 1 | a0001c0001t0002g0247 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.142-3290T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541246 | |||||||
chr4:83541376 | C | A | 1 | a0002c0002t0003g0248 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.142-3160C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541376 | |||||||
chr4:83541393 | C | CT | 17 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0176 others(14): Show |
17 | HG01175.hp2 HG02055.hp1 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.142-3123dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83541393 | ||||||
chr4:83541393 | C | CTT | 86 | a0001c0001t0001g0238 a0001c0001t0001g0241 a0001c0001t0001g0254 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.142-3124_142-3123d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83541393 | ||||||
chr4:83541393 | C | CTTT | 8 | a0001c0001t0001g0240 a0001c0001t0002g0317 a0001c0001t0002g0319 others(5): Show |
8 | HG00642.hp2 HG02559.hp2 HG04184.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-3125_142-3123d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83541393 | ||||||
chr4:83541393 | CT | C | 30 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0208 others(27): Show |
30 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-3123delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83541393 | ||||||
chr4:83541451 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.142-3085C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541451 | |||||||
chr4:83541672 | G | A | 1 | a0001c0001t0002g0330 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.142-2864G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541672 | |||||||
chr4:83541759 | C | A | 1 | a0001c0001t0003g0030 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.142-2777C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541759 | |||||||
chr4:83541792 | C | T | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-2744C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541792 | |||||||
chr4:83541874 | G | A | 2 | a0001c0001t0003g0183 a0001c0001t0005g0182 |
2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.142-2662G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83541874 | |||||||
chr4:83542013 | A | G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0177 |
3 | NA18949.hp2 NA18977.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.142-2523A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542013 | |||||||
chr4:83542041 | T | TG | 6 | a0001c0001t0002g0330 a0001c0001t0003g0183 a0001c0001t0005g0182 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-2490dupG | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr4 | 83542041 | ||||||
chr4:83542056 | C | T | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-2480C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542056 | |||||||
chr4:83542089 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.142-2447C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542089 | |||||||
chr4:83542740 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.142-1796A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542740 | |||||||
chr4:83542814 | A | G | 31 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0208 others(28): Show |
31 | HG00099.hp1 HG00280.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.142-1722A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542814 | |||||||
chr4:83542851 | G | A | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-1685G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542851 | |||||||
chr4:83542871 | G | C | 1 | a0001c0001t0002g0252 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.142-1665G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542871 | |||||||
chr4:83542937 | G | A | 19 | a0001c0001t0001g0008 a0001c0001t0002g0007 a0001c0001t0002g0009 others(16): Show |
19 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.142-1599G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542937 | |||||||
chr4:83542986 | G | A | 6 | a0001c0001t0002g0330 a0001c0001t0003g0183 a0001c0001t0005g0182 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-1550G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542986 | |||||||
chr4:83542993 | C | G | 2 | a0001c0001t0002g0332 a0001c0001t0005g0331 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.142-1543C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83542993 | |||||||
chr4:83543030 | T | G | 163 | a0001c0001t0001g0008 a0001c0001t0001g0216 a0001c0001t0001g0217 others(160): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.142-1506T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543030 | |||||||
chr4:83543038 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.142-1498C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543038 | |||||||
chr4:83543059 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.142-1477G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543059 | |||||||
chr4:83543283 | C | T | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-1253C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543283 | |||||||
chr4:83543319 | G | A | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-1217G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543319 | |||||||
chr4:83543322 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142-1214C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543322 | |||||||
chr4:83543337 | G | C | 6 | a0001c0001t0002g0330 a0001c0001t0003g0183 a0001c0001t0005g0182 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-1199G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543337 | |||||||
chr4:83543471 | C | T | 2 | a0001c0001t0014g0181 a0001c0001t0015g0180 |
2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.142-1065C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543471 | |||||||
chr4:83543521 | C | T | 1 | a0001c0001t0002g0330 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.142-1015C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543521 | |||||||
chr4:83543857 | T | C | 1 | a0001c0001t0002g0317 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.142-679T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543857 | |||||||
chr4:83543880 | A | T | 1 | a0001c0001t0002g0316 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.142-656A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543880 | |||||||
chr4:83543997 | A | G | 3 | a0001c0001t0003g0183 a0001c0001t0005g0182 a0001c0001t0005g0184 |
3 | HG02258.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.142-539A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83543997 | |||||||
chr4:83544083 | C | T | 95 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(92): Show |
95 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.142-453C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544083 | |||||||
chr4:83544241 | C | A | 1 | a0001c0001t0002g0222 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.142-295C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544241 | |||||||
chr4:83544308 | G | A | 1 | a0001c0001t0005g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142-228G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544308 | |||||||
chr4:83544316 | A | G | 5 | a0001c0001t0007g0188 a0001c0001t0007g0189 a0001c0001t0007g0190 others(2): Show |
5 | HG02622.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-220A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544316 | |||||||
chr4:83544460 | C | T | 94 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.142-76C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544460 | |||||||
chr4:83544501 | G | C | 1 | a0001c0001t0006g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-35G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 1/11 | chr4 | 83544501 | |||||||
chr4:83544702 | A | C | 94 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.208+100A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83544702 | |||||||
chr4:83544730 | C | A | 1 | a0001c0001t0005g0318 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.208+128C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83544730 | |||||||
chr4:83544863 | G | A | 3 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 |
3 | HG02145.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.208+261G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83544863 | |||||||
chr4:83545076 | A | T | 3 | a0001c0001t0002g0247 a0001c0001t0002g0314 a0001c0001t0002g0315 |
3 | HG02004.hp2 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.208+474A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545076 | |||||||
chr4:83545178 | C | T | 4 | a0001c0001t0002g0332 a0001c0001t0003g0194 a0001c0001t0004g0195 others(1): Show |
4 | HG02451.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+576C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545178 | |||||||
chr4:83545247 | C | A | 1 | a0001c0001t0003g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.208+645C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545247 | |||||||
chr4:83545261 | C | T | 3 | a0001c0001t0003g0183 a0001c0001t0005g0182 a0001c0001t0005g0184 |
3 | HG02258.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.208+659C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545261 | |||||||
chr4:83545444 | T | TA | 114 | a0001c0001t0001g0008 a0001c0001t0001g0238 a0001c0001t0001g0240 others(111): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.208+856dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83545444 | ||||||
chr4:83545569 | A | C | 2 | a0001c0001t0003g0194 a0001c0001t0004g0195 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.208+967A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545569 | |||||||
chr4:83545589 | T | G | 2 | a0001c0001t0003g0194 a0001c0001t0004g0195 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.208+987T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545589 | |||||||
chr4:83545603 | G | A | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.208+1001G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545603 | |||||||
chr4:83545757 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.208+1155C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545757 | |||||||
chr4:83545825 | A | G | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.208+1223A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545825 | |||||||
chr4:83545917 | T | G | 2 | a0001c0001t0002g0332 a0001c0001t0005g0331 |
2 | HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.208+1315T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83545917 | |||||||
chr4:83546120 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.208+1518G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546120 | |||||||
chr4:83546147 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.208+1545G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546147 | |||||||
chr4:83546223 | G | A | 1 | a0001c0001t0002g0319 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.208+1621G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546223 | |||||||
chr4:83546307 | C | T | 2 | a0001c0001t0003g0194 a0001c0001t0004g0195 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.208+1705C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546307 | |||||||
chr4:83546379 | G | GT | 104 | a0001c0001t0001g0027 a0001c0001t0001g0162 a0001c0001t0001g0163 others(101): Show |
104 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.208+1793dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83546379 | ||||||
chr4:83546379 | GT | G | 6 | a0001c0001t0001g0008 a0001c0001t0003g0005 a0001c0001t0003g0183 others(3): Show |
6 | HG00733.hp2 HG02258.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+1793delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83546379 | ||||||
chr4:83546488 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0035 |
3 | HG00741.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.208+1886T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546488 | |||||||
chr4:83546584 | C | T | 3 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 |
3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.208+1982C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546584 | |||||||
chr4:83546594 | G | A | 94 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.208+1992G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546594 | |||||||
chr4:83546698 | C | T | 94 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.208+2096C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546698 | |||||||
chr4:83546710 | A | G | 94 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.208+2108A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546710 | |||||||
chr4:83546771 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.208+2169G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546771 | |||||||
chr4:83546791 | T | C | 1 | a0001c0001t0005g0196 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208+2189T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83546791 | |||||||
chr4:83547003 | C | T | 29 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0208 others(26): Show |
29 | HG00099.hp1 HG00280.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.208+2401C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547003 | |||||||
chr4:83547064 | C | T | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.208+2462C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547064 | |||||||
chr4:83547246 | C | CT | 25 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0155 others(22): Show |
25 | HG00642.hp2 HG00741.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.208+2668dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83547246 | ||||||
chr4:83547246 | CT | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0070 a0001c0001t0001g0076 others(32): Show |
35 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.208+2668delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83547246 | ||||||
chr4:83547246 | CTT | C | 78 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(75): Show |
79 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.208+2667_208+2668d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83547246 | ||||||
chr4:83547283 | T | C | 92 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(89): Show |
92 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.208+2681T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547283 | |||||||
chr4:83547286 | T | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0070 a0001c0001t0001g0083 others(5): Show |
8 | NA18939.hp1 NA18960.hp2 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+2684T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547286 | |||||||
chr4:83547292 | A | G | 3 | a0001c0001t0005g0198 a0001c0001t0007g0189 a0001c0001t0007g0190 |
3 | HG02622.hp2 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.208+2690A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547292 | |||||||
chr4:83547341 | C | T | 4 | a0001c0001t0004g0306 a0001c0001t0005g0239 a0001c0001t0005g0245 others(1): Show |
4 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+2739C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547341 | |||||||
chr4:83547346 | A | G | 4 | a0001c0001t0004g0306 a0001c0001t0005g0239 a0001c0001t0005g0245 others(1): Show |
4 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+2744A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547346 | |||||||
chr4:83547348 | A | G | 6 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0004g0306 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+2746A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547348 | |||||||
chr4:83547397 | T | C | 8 | a0001c0001t0003g0197 a0001c0001t0004g0199 a0001c0001t0004g0200 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+2795T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547397 | |||||||
chr4:83547402 | G | A | 3 | a0001c0001t0003g0006 a0001c0001t0003g0015 a0001c0001t0003g0016 |
3 | HG00642.hp1 HG00741.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.208+2800G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547402 | |||||||
chr4:83547410 | G | A | 1 | a0001c0001t0014g0181 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.208+2808G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547410 | |||||||
chr4:83547414 | A | G | 1 | a0001c0001t0002g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.208+2812A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547414 | |||||||
chr4:83547453 | C | A | 1 | a0001c0001t0001g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.208+2851C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547453 | |||||||
chr4:83547463 | A | C | 1 | a0001c0001t0001g0154 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.208+2861A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547463 | |||||||
chr4:83547463 | A | G | 1 | a0001c0001t0002g0329 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.208+2861A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547463 | |||||||
chr4:83547464 | G | A | 14 | a0001c0001t0002g0024 a0001c0001t0003g0036 a0001c0001t0003g0037 others(11): Show |
14 | HG00438.hp2 HG00597.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.208+2862G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547464 | |||||||
chr4:83547479 | C | T | 142 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0051 others(139): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.208+2877C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547479 | |||||||
chr4:83547487 | T | C | 7 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0001t0002g0260 others(4): Show |
7 | HG00099.hp1 HG02717.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+2885T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547487 | |||||||
chr4:83547494 | T | C | 2 | a0001c0001t0002g0330 a0001c0001t0005g0205 |
2 | HG00099.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.208+2892T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547494 | |||||||
chr4:83547499 | A | G | 236 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0051 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.208+2897A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547499 | |||||||
chr4:83547503 | C | T | 209 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0052 others(206): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.208+2901C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547503 | |||||||
chr4:83547504 | G | A | 209 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0052 others(206): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.208+2902G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547504 | |||||||
chr4:83547532 | G | A | 175 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0052 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.208+2930G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547532 | |||||||
chr4:83547538 | T | C | 8 | a0001c0001t0003g0197 a0001c0001t0004g0199 a0001c0001t0004g0200 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+2936T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547538 | |||||||
chr4:83547547 | T | C | 2 | a0001c0001t0002g0247 a0001c0001t0002g0263 |
2 | HG00408.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.208+2945T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547547 | |||||||
chr4:83547806 | C | A | 2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | NA18951.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.208+3204C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547806 | |||||||
chr4:83547806 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.208+3204C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547806 | |||||||
chr4:83547807 | G | A | 5 | a0001c0001t0004g0306 a0001c0001t0005g0196 a0001c0001t0005g0239 others(2): Show |
5 | HG01243.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+3205G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83547807 | |||||||
chr4:83547853 | CT | C | 76 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0064 others(73): Show |
77 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.208+3268delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83547853 | ||||||
chr4:83547853 | CTT | C | 118 | a0001c0001t0001g0051 a0001c0001t0001g0216 a0001c0001t0001g0217 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.208+3267_208+3268d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83547853 | ||||||
chr4:83548053 | C | G | 1 | a0001c0001t0005g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.208+3451C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548053 | |||||||
chr4:83548285 | T | C | 5 | a0001c0001t0003g0183 a0001c0001t0003g0194 a0001c0001t0004g0309 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+3683T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548285 | |||||||
chr4:83548699 | C | T | 73 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(70): Show |
74 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.208+4097C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548699 | |||||||
chr4:83548917 | C | G | 73 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(70): Show |
74 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.208+4315C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548917 | |||||||
chr4:83548983 | T | A | 1 | a0001c0001t0003g0161 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.208+4381T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548983 | |||||||
chr4:83548990 | AC | A | 21 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.208+4389delC | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83548990 | |||||||
chr4:83549031 | A | C | 1 | a0001c0001t0005g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.208+4429A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549031 | |||||||
chr4:83549038 | GTGACAGA others(13): Show |
G | 1 | a0001c0001t0005g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.208+4438_208+4457d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549038 | ||||||
chr4:83549160 | C | A | 1 | a0001c0001t0002g0257 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.208+4558C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549160 | |||||||
chr4:83549166 | G | GAAA | 112 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(109): Show |
112 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.208+4576_208+4578d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549166 | ||||||
chr4:83549166 | GA | G | 14 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(11): Show |
14 | HG00099.hp1 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+4578delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549166 | ||||||
chr4:83549229 | T | A | 1 | a0001c0001t0013g0171 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.208+4627T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549229 | |||||||
chr4:83549444 | C | CGT | 69 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0064 others(66): Show |
70 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.208+4865_208+4866d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549444 | ||||||
chr4:83549444 | C | CGTGT | 23 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(20): Show |
23 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.208+4863_208+4866d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549444 | ||||||
chr4:83549444 | CGT | C | 4 | a0001c0001t0002g0215 a0001c0001t0005g0205 a0001c0001t0005g0225 others(1): Show |
4 | HG00099.hp1 HG03710.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+4865_208+4866d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549444 | ||||||
chr4:83549444 | CGTGT | C | 3 | a0001c0001t0004g0195 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG02451.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.208+4863_208+4866d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549444 | ||||||
chr4:83549465 | GTGTA | G | 15 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0009 others(12): Show |
15 | HG00140.hp1 HG01109.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.208+4869_208+4872d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549465 | ||||||
chr4:83549467 | GTA | G | 79 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(76): Show |
79 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.208+4867_208+4868d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549467 | ||||||
chr4:83549469 | A | G | 21 | a0001c0001t0002g0210 a0001c0001t0002g0226 a0001c0001t0002g0228 others(18): Show |
21 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.208+4867A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549469 | |||||||
chr4:83549471 | GTATA | G | 4 | a0001c0001t0002g0210 a0001c0001t0002g0226 a0001c0001t0002g0311 others(1): Show |
4 | HG01884.hp1 HG02145.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+4877_208+4880d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549471 | ||||||
chr4:83549473 | A | G | 111 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(108): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.208+4871A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549473 | |||||||
chr4:83549475 | A | G | 11 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+4873A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549475 | |||||||
chr4:83549477 | A | G | 11 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+4875A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549477 | |||||||
chr4:83549479 | A | G | 11 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(8): Show |
11 | HG02055.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+4877A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549479 | |||||||
chr4:83549620 | C | G | 1 | a0001c0001t0004g0204 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.208+5018C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549620 | |||||||
chr4:83549622 | T | C | 1 | a0001c0001t0004g0204 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.208+5020T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549622 | |||||||
chr4:83549623 | C | T | 1 | a0001c0001t0004g0204 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.208+5021C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549623 | |||||||
chr4:83549680 | T | C | 189 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.208+5078T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549680 | |||||||
chr4:83549711 | T | TTTA | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(4): Show |
7 | HG02257.hp1 HG02602.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+5124_208+5126d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | ||||||
chr4:83549711 | T | TTTATTA | 92 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(89): Show |
92 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.208+5121_208+5126d others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | ||||||
chr4:83549711 | T | TTTATTAT others(2): Show |
6 | a0001c0001t0002g0247 a0001c0001t0002g0258 a0001c0001t0002g0266 others(3): Show |
6 | HG00099.hp2 HG01256.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+5118_208+5126d others(11): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | ||||||
chr4:83549711 | T | TTTATTAT others(5): Show |
1 | a0001c0001t0002g0314 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.208+5115_208+5126d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | ||||||
chr4:83549711 | T | TTTATTAT others(8): Show |
3 | a0001c0001t0005g0014 a0001c0001t0012g0243 a0001c0004t0004g0305 |
3 | HG03041.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208+5112_208+5126d others(17): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | ||||||
chr4:83549711 | T | TTTATTAT others(11): Show |
6 | a0001c0001t0002g0231 a0001c0001t0002g0232 a0001c0001t0002g0233 others(3): Show |
6 | HG02055.hp1 HG02922.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+5126_208+5127i others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | ||||||
chr4:83549711 | T | TTTATTAT others(14): Show |
4 | a0001c0001t0002g0230 a0001c0001t0002g0234 a0001c0001t0002g0235 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+5126_208+5127i others(23): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | ||||||
chr4:83549711 | T | TTTATTAT others(20): Show |
2 | a0001c0001t0002g0228 a0001c0001t0002g0229 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.208+5126_208+5127i others(29): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83549711 | ||||||
chr4:83549729 | G | A | 187 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.208+5127G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549729 | |||||||
chr4:83549822 | A | G | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0177 |
3 | NA18949.hp2 NA18977.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.208+5220A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83549822 | |||||||
chr4:83550100 | AGTGATTC others(19): Show |
A | 1 | a0001c0001t0004g0204 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.208+5502_208+5527d others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83550100 | ||||||
chr4:83551109 | C | T | 2 | a0001c0001t0003g0081 a0001c0001t0003g0175 |
2 | HG01081.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.208+6507C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551109 | |||||||
chr4:83551118 | A | G | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.208+6516A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551118 | |||||||
chr4:83551315 | A | G | 1 | a0001c0001t0015g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.208+6713A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551315 | |||||||
chr4:83551487 | ATT | A | 105 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(102): Show |
105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.208+6892_208+6893d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551487 | ||||||
chr4:83551490 | T | A | 105 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(102): Show |
105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.208+6888T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551490 | |||||||
chr4:83551603 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.208+7001C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551603 | |||||||
chr4:83551662 | C | T | 73 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(70): Show |
74 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.208+7060C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551662 | |||||||
chr4:83551665 | C | A | 115 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.208+7063C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551665 | |||||||
chr4:83551706 | C | T | 1 | a0001c0001t0004g0221 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.208+7104C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551706 | |||||||
chr4:83551793 | G | GA | 12 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0148 others(9): Show |
12 | HG01175.hp1 HG02615.hp1 HG02698.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+7212dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551793 | ||||||
chr4:83551793 | GA | G | 14 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0151 others(11): Show |
14 | HG01496.hp2 HG02015.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+7212delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551793 | ||||||
chr4:83551813 | A | AAAAATCT others(8): Show |
3 | a0001c0001t0001g0216 a0001c0001t0005g0014 a0001c0001t0005g0211 |
3 | HG02572.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208+7212_208+7213i others(17): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAAAATCT others(16): Show |
4 | a0001c0001t0002g0226 a0001c0001t0002g0246 a0001c0001t0002g0310 others(1): Show |
4 | HG02027.hp2 HG02145.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(25): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAAATCTA others(3): Show |
2 | a0001c0001t0002g0250 a0001c0001t0002g0275 |
2 | HG03490.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.208+7212_208+7213i others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAAATCTA others(7): Show |
18 | a0001c0001t0001g0217 a0001c0001t0001g0238 a0001c0001t0001g0240 others(15): Show |
18 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAAATCTA others(11): Show |
25 | a0001c0001t0001g0297 a0001c0001t0001g0300 a0001c0001t0002g0010 others(22): Show |
25 | HG01070.hp2 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAAATCTA others(15): Show |
27 | a0001c0001t0001g0307 a0001c0001t0002g0009 a0001c0001t0002g0049 others(24): Show |
27 | HG00099.hp2 HG01192.hp1 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAAATCTA others(19): Show |
1 | a0001c0001t0002g0323 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.208+7212_208+7213i others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAATCT | 6 | a0001c0001t0001g0089 a0001c0001t0003g0183 a0001c0001t0003g0194 others(3): Show |
6 | HG02258.hp1 HG03209.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAATCTAT others(2): Show |
15 | a0001c0001t0002g0024 a0001c0001t0002g0249 a0001c0001t0002g0259 others(12): Show |
15 | HG00438.hp2 HG01993.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(11): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAATCTAT others(6): Show |
10 | a0001c0001t0002g0242 a0001c0001t0002g0251 a0001c0001t0002g0256 others(7): Show |
10 | HG00408.hp1 NA18944.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.208+7212_208+7213i others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAATCTAT others(10): Show |
2 | a0001c0001t0002g0258 a0001c0001t0002g0276 |
2 | HG02040.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.208+7212_208+7213i others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AAATCTAT others(14): Show |
1 | a0001c0001t0003g0327 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.208+7212_208+7213i others(23): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AATCT | 21 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(18): Show |
21 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.208+7244_208+7247d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AATCTATC others(1): Show |
16 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(13): Show |
16 | HG02055.hp2 HG02486.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.208+7240_208+7247d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AATCTATC others(5): Show |
3 | a0001c0001t0002g0215 a0001c0001t0002g0286 a0001c0001t0009g0187 |
3 | HG03130.hp1 HG03710.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.208+7236_208+7247d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | A | AATCTATC others(9): Show |
2 | a0001c0001t0005g0225 a0001c0001t0009g0186 |
2 | NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.208+7232_208+7247d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551813 | AATCTATC others(5): Show |
A | 3 | a0001c0001t0005g0004 a0001c0001t0014g0181 a0001c0001t0015g0180 |
3 | HG02055.hp1 HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.208+7236_208+7247d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83551813 | ||||||
chr4:83551814 | ATCTATCT others(4): Show |
A | 10 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(7): Show |
10 | HG01891.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+7213_208+7223d others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551814 | |||||||
chr4:83551959 | G | A | 1 | a0001c0001t0002g0330 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.208+7357G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551959 | |||||||
chr4:83551999 | G | C | 1 | a0001c0001t0005g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.208+7397G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83551999 | |||||||
chr4:83552078 | C | G | 2 | a0001c0001t0003g0057 a0001c0001t0003g0170 |
2 | NA18977.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.208+7476C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552078 | |||||||
chr4:83552208 | C | T | 3 | a0001c0001t0002g0310 a0001c0001t0002g0313 a0001c0001t0002g0322 |
3 | NA18947.hp2 NA18975.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.208+7606C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552208 | |||||||
chr4:83552238 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0151 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.208+7636G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552238 | |||||||
chr4:83552286 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.208+7684C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552286 | |||||||
chr4:83552423 | G | A | 5 | a0001c0001t0002g0215 a0001c0001t0005g0205 a0001c0001t0005g0225 others(2): Show |
5 | HG00099.hp1 HG03130.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+7821G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552423 | |||||||
chr4:83552760 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.208+8158C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552760 | |||||||
chr4:83552950 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.208+8348C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83552950 | |||||||
chr4:83553088 | A | G | 2 | a0001c0001t0014g0181 a0001c0001t0015g0180 |
2 | HG02055.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.208+8486A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553088 | |||||||
chr4:83553095 | T | C | 17 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(14): Show |
17 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+8493T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553095 | |||||||
chr4:83553223 | T | C | 10 | a0001c0001t0004g0306 a0001c0001t0005g0014 a0001c0001t0005g0196 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+8621T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553223 | |||||||
chr4:83553226 | T | C | 17 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(14): Show |
17 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+8624T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553226 | |||||||
chr4:83553421 | A | G | 5 | a0001c0001t0003g0183 a0001c0001t0003g0194 a0001c0001t0004g0309 others(2): Show |
5 | HG02109.hp1 HG02258.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+8819A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553421 | |||||||
chr4:83553442 | T | C | 6 | a0001c0001t0002g0082 a0001c0001t0002g0259 a0001c0001t0002g0260 others(3): Show |
6 | NA18943.hp2 NA18948.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+8840T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553442 | |||||||
chr4:83553481 | G | A | 10 | a0001c0001t0004g0306 a0001c0001t0005g0014 a0001c0001t0005g0196 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+8879G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553481 | |||||||
chr4:83553593 | A | G | 10 | a0001c0001t0004g0306 a0001c0001t0005g0014 a0001c0001t0005g0196 others(7): Show |
10 | HG01243.hp1 HG01891.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+8991A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553593 | |||||||
chr4:83553616 | AG | A | 7 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+9016delG | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83553616 | ||||||
chr4:83553641 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208+9039G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553641 | |||||||
chr4:83553814 | G | A | 32 | a0001c0001t0001g0050 a0001c0001t0003g0025 a0001c0001t0003g0030 others(29): Show |
32 | HG00597.hp1 HG00609.hp1 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.208+9212G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553814 | |||||||
chr4:83553843 | C | G | 7 | a0001c0001t0001g0077 a0001c0001t0001g0130 a0001c0001t0001g0131 others(4): Show |
7 | HG01168.hp1 HG01169.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+9241C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553843 | |||||||
chr4:83553972 | A | T | 2 | a0001c0001t0003g0293 a0001c0001t0003g0301 |
2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.208+9370A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83553972 | |||||||
chr4:83554504 | A | C | 5 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG01081.hp1 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+9902A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83554504 | |||||||
chr4:83554741 | T | C | 1 | a0001c0001t0006g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.208+10139T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83554741 | |||||||
chr4:83554801 | C | CT | 53 | a0001c0001t0001g0086 a0001c0001t0001g0133 a0001c0001t0001g0164 others(50): Show |
53 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.208+10219dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83554801 | ||||||
chr4:83554801 | CTTT | C | 75 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(72): Show |
76 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.208+10217_208+1021 others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83554801 | ||||||
chr4:83554964 | C | T | 6 | a0001c0001t0001g0076 a0001c0001t0001g0090 a0001c0001t0001g0097 others(3): Show |
6 | HG02698.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+10362C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83554964 | |||||||
chr4:83555004 | A | C | 6 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0095 others(3): Show |
6 | HG00438.hp1 HG00609.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+10402A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555004 | |||||||
chr4:83555043 | A | T | 8 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+10441A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555043 | |||||||
chr4:83555150 | T | C | 2 | a0001c0001t0003g0183 a0001c0001t0005g0182 |
2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.208+10548T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555150 | |||||||
chr4:83555208 | A | G | 18 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(15): Show |
18 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+10606A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555208 | |||||||
chr4:83555394 | TTTAATCA others(10): Show |
T | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+10793_208+1080 others(21): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555394 | |||||||
chr4:83555470 | A | G | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+10868A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555470 | |||||||
chr4:83555562 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.208+10960G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555562 | |||||||
chr4:83555625 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.208+11023G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555625 | |||||||
chr4:83555707 | C | T | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+11105C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555707 | |||||||
chr4:83555790 | G | A | 6 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+11188G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555790 | |||||||
chr4:83555809 | T | C | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+11207T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555809 | |||||||
chr4:83555824 | A | G | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+11222A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555824 | |||||||
chr4:83555840 | A | G | 2 | a0001c0001t0003g0067 a0001c0001t0003g0068 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.208+11238A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83555840 | |||||||
chr4:83556095 | A | G | 2 | a0001c0001t0010g0244 a0001c0001t0010g0267 |
2 | HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.208+11493A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556095 | |||||||
chr4:83556122 | A | G | 1 | a0001c0001t0003g0043 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.208+11520A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556122 | |||||||
chr4:83556245 | T | C | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.208+11643T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556245 | |||||||
chr4:83556390 | T | C | 1 | a0001c0001t0003g0056 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.208+11788T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556390 | |||||||
chr4:83556562 | A | ATT | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+11968_208+1196 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83556562 | ||||||
chr4:83556782 | CA | C | 6 | a0001c0001t0001g0080 a0001c0001t0001g0088 a0001c0001t0002g0323 others(3): Show |
6 | HG02258.hp1 HG02818.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+12194delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83556782 | ||||||
chr4:83556937 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.208+12335C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556937 | |||||||
chr4:83556989 | C | G | 103 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(100): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.208+12387C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83556989 | |||||||
chr4:83557036 | C | T | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12434C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557036 | |||||||
chr4:83557103 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.208+12501C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557103 | |||||||
chr4:83557119 | T | G | 5 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+12517T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557119 | |||||||
chr4:83557272 | C | A | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12670C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557272 | |||||||
chr4:83557332 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0150 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.208+12730A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557332 | |||||||
chr4:83557359 | T | C | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12757T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557359 | |||||||
chr4:83557463 | G | C | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12861G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557463 | |||||||
chr4:83557511 | A | G | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12909A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557511 | |||||||
chr4:83557518 | TA | T | 86 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(83): Show |
87 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.208+12925delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83557518 | ||||||
chr4:83557527 | A | T | 66 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(63): Show |
67 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.208+12925A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557527 | |||||||
chr4:83557583 | A | G | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+12981A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557583 | |||||||
chr4:83557726 | A | G | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208+13124A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557726 | |||||||
chr4:83557834 | T | C | 1 | a0001c0001t0006g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.208+13232T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557834 | |||||||
chr4:83557890 | T | C | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208+13288T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557890 | |||||||
chr4:83557907 | C | T | 6 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+13305C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557907 | |||||||
chr4:83557909 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.208+13307G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557909 | |||||||
chr4:83557967 | C | G | 18 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(15): Show |
18 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+13365C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83557967 | |||||||
chr4:83558071 | G | A | 5 | a0001c0001t0002g0082 a0001c0001t0002g0259 a0001c0001t0002g0260 others(2): Show |
5 | NA18943.hp2 NA18948.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+13469G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558071 | |||||||
chr4:83558213 | T | A | 1 | a0001c0001t0003g0037 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.208+13611T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558213 | |||||||
chr4:83558213 | T | C | 103 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(100): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.208+13611T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558213 | |||||||
chr4:83558249 | TG | T | 4 | a0001c0001t0003g0183 a0001c0001t0003g0194 a0001c0001t0005g0182 others(1): Show |
4 | HG02258.hp1 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+13648delG | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558249 | |||||||
chr4:83558256 | A | G | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+13654A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558256 | |||||||
chr4:83558319 | T | G | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.208+13717T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558319 | |||||||
chr4:83558435 | A | T | 12 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 others(9): Show |
12 | HG01243.hp1 HG02630.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.208+13833A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558435 | |||||||
chr4:83558540 | G | A | 82 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(79): Show |
83 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.208+13938G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558540 | |||||||
chr4:83558765 | G | A | 101 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.208+14163G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558765 | |||||||
chr4:83558874 | C | T | 2 | a0001c0001t0003g0067 a0001c0001t0003g0068 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.208+14272C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83558874 | |||||||
chr4:83559046 | A | G | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208+14444A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559046 | |||||||
chr4:83559099 | A | C | 100 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(97): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.208+14497A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559099 | |||||||
chr4:83559120 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.208+14518G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559120 | |||||||
chr4:83559304 | A | G | 327 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0023 others(324): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.208+14702A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559304 | |||||||
chr4:83559322 | G | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0191 |
2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.208+14720G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559322 | |||||||
chr4:83559347 | A | G | 29 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(26): Show |
29 | HG00099.hp1 HG01243.hp1 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.208+14745A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559347 | |||||||
chr4:83559426 | C | T | 3 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0206 |
3 | HG01891.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.208+14824C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559426 | |||||||
chr4:83559468 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.208+14866C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559468 | |||||||
chr4:83559489 | A | G | 1 | a0001c0001t0006g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.208+14887A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559489 | |||||||
chr4:83559575 | C | T | 29 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(26): Show |
29 | HG00099.hp1 HG01243.hp1 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.208+14973C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559575 | |||||||
chr4:83559579 | C | G | 29 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(26): Show |
29 | HG00099.hp1 HG01243.hp1 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.208+14977C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559579 | |||||||
chr4:83559678 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.208+15076G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559678 | |||||||
chr4:83559757 | C | T | 1 | a0001c0001t0004g0306 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.208+15155C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559757 | |||||||
chr4:83559831 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(67): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.208+15229C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83559831 | |||||||
chr4:83560100 | C | T | 1 | a0001c0001t0004g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.208+15498C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560100 | |||||||
chr4:83560116 | C | T | 11 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(8): Show |
11 | HG00099.hp1 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.208+15514C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560116 | |||||||
chr4:83560294 | G | A | 1 | a0001c0001t0006g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.208+15692G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560294 | |||||||
chr4:83560418 | AT | A | 22 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(19): Show |
22 | HG00099.hp1 HG01243.hp1 HG02615.hp1 others(19): Show |
intron_variant | MODIFIER | c.208+15826delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83560418 | ||||||
chr4:83560549 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.208+15947G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560549 | |||||||
chr4:83560704 | G | C | 18 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(15): Show |
18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+16102G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560704 | |||||||
chr4:83560934 | C | T | 18 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(15): Show |
18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+16332C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560934 | |||||||
chr4:83560965 | G | A | 18 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(15): Show |
18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+16363G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83560965 | |||||||
chr4:83561034 | C | T | 3 | a0001c0001t0002g0266 a0001c0001t0010g0244 a0001c0001t0010g0267 |
3 | HG00099.hp2 HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.208+16432C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561034 | |||||||
chr4:83561052 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.208+16450G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561052 | |||||||
chr4:83561177 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.208+16575C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561177 | |||||||
chr4:83561234 | G | C | 224 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.208+16632G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561234 | |||||||
chr4:83561301 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.208+16699A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561301 | |||||||
chr4:83561482 | C | T | 18 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(15): Show |
18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+16880C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561482 | |||||||
chr4:83561514 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0134 |
2 | NA18959.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.208+16912G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561514 | |||||||
chr4:83561587 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.208+16985A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561587 | |||||||
chr4:83561664 | A | C | 18 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(15): Show |
18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+17062A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561664 | |||||||
chr4:83561680 | A | G | 1 | a0001c0001t0005g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.208+17078A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561680 | |||||||
chr4:83561819 | A | AAG | 23 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(20): Show |
23 | HG00099.hp1 HG01243.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.208+17227_208+1722 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83561819 | ||||||
chr4:83561929 | C | T | 1 | a0001c0001t0003g0321 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.208+17327C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83561929 | |||||||
chr4:83562027 | A | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0164 |
2 | HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.208+17425A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562027 | |||||||
chr4:83562081 | G | A | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+17479G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562081 | |||||||
chr4:83562108 | C | G | 8 | a0001c0001t0005g0198 a0001c0001t0006g0002 a0001c0001t0006g0003 others(5): Show |
8 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.208+17506C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562108 | |||||||
chr4:83562172 | T | TTATATAT others(57): Show |
2 | a0002c0002t0003g0145 a0002c0002t0003g0146 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.208+17623_208+1762 others(68): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562172 | ||||||
chr4:83562179 | T | TTA | 3 | a0001c0001t0001g0125 a0001c0001t0001g0155 a0001c0001t0001g0164 |
3 | HG02523.hp2 NA18939.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.208+17596_208+1759 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562179 | ||||||
chr4:83562179 | T | TTATATAT others(27): Show |
1 | a0001c0001t0001g0116 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.208+17590_208+1762 others(38): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562179 | ||||||
chr4:83562179 | TTA | T | 92 | a0001c0001t0001g0101 a0001c0001t0001g0238 a0001c0001t0001g0240 others(89): Show |
92 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.208+17596_208+1759 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562179 | ||||||
chr4:83562181 | A | ATATATAT others(23): Show |
5 | a0001c0001t0001g0079 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG01081.hp1 HG01884.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+17594_208+1762 others(34): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562181 | ||||||
chr4:83562183 | A | ATATATAT others(17): Show |
1 | a0001c0001t0005g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.208+17593_208+1759 others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562183 | ||||||
chr4:83562183 | A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0148 a0001c0001t0001g0150 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.208+17596_208+1762 others(32): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562183 | ||||||
chr4:83562183 | A | ATATATAT others(49): Show |
1 | a0001c0001t0001g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208+17623_208+1762 others(60): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562183 | ||||||
chr4:83562183 | A | ATATATAT others(51): Show |
1 | a0001c0001t0001g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.208+17623_208+1762 others(62): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562183 | ||||||
chr4:83562183 | A | ATATATAT others(53): Show |
1 | a0001c0001t0001g0080 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.208+17623_208+1762 others(64): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562183 | ||||||
chr4:83562188 | T | TATATATA others(39): Show |
1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.208+17595_208+1759 others(50): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562188 | ||||||
chr4:83562188 | T | TATATATA others(30): Show |
1 | a0001c0001t0008g0075 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.208+17610_208+1764 others(41): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562188 | ||||||
chr4:83562190 | TATATATA others(24): Show |
T | 2 | a0001c0001t0001g0051 a0001c0001t0003g0016 |
2 | HG00642.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.208+17589_208+1761 others(35): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562190 | |||||||
chr4:83562190 | TATATATA others(29): Show |
T | 65 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0064 others(62): Show |
66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.208+17589_208+1762 others(40): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562190 | |||||||
chr4:83562190 | TATATATA others(33): Show |
T | 2 | a0001c0001t0003g0056 a0001c0001t0003g0326 |
2 | HG04228.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.208+17589_208+1762 others(44): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562190 | |||||||
chr4:83562192 | TATATATA others(26): Show |
T | 2 | a0001c0001t0005g0014 a0001c0001t0012g0243 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.208+17598_208+1763 others(37): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562192 | ||||||
chr4:83562193 | ATATATAA others(38): Show |
A | 7 | a0001c0001t0005g0198 a0001c0001t0006g0002 a0001c0001t0006g0003 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+17592_208+1763 others(49): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562193 | |||||||
chr4:83562194 | T | TA | 17 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0009 others(14): Show |
17 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+17593dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562194 | ||||||
chr4:83562195 | ATATAATA others(36): Show |
A | 1 | a0001c0001t0005g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.208+17594_208+1763 others(47): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562195 | |||||||
chr4:83562195 | ATATAATA others(38): Show |
A | 1 | a0001c0001t0006g0212 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.208+17594_208+1763 others(49): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562195 | |||||||
chr4:83562196 | TATA | T | 3 | a0001c0001t0002g0007 a0001c0001t0002g0021 a0001c0001t0002g0192 |
3 | HG02486.hp2 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.208+17598_208+1760 others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562196 | ||||||
chr4:83562196 | TATAATAT others(22): Show |
T | 3 | a0001c0001t0004g0013 a0001c0001t0004g0306 a0001c0001t0005g0245 |
3 | HG01243.hp1 HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.208+17598_208+1762 others(33): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562196 | ||||||
chr4:83562198 | T | A | 9 | a0001c0001t0001g0135 a0001c0001t0003g0197 a0001c0001t0004g0199 others(6): Show |
9 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.208+17596T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562198 | |||||||
chr4:83562198 | TAATATAT others(20): Show |
T | 6 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 others(3): Show |
6 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+17598_208+1762 others(31): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562198 | ||||||
chr4:83562199 | A | AT | 17 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0009 others(14): Show |
17 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+17597_208+1759 others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562199 | |||||||
chr4:83562199 | A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208+17597_208+1759 others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562199 | |||||||
chr4:83562199 | A | T | 8 | a0001c0001t0003g0197 a0001c0001t0004g0199 a0001c0001t0004g0200 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+17597A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562199 | |||||||
chr4:83562199 | AATATATA others(5): Show |
A | 1 | a0001c0001t0002g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208+17598_208+1760 others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562199 | |||||||
chr4:83562199 | AATATATA others(18): Show |
A | 3 | a0001c0001t0005g0196 a0001c0001t0005g0318 a0001c0001t0005g0333 |
3 | HG02896.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.208+17599_208+1762 others(29): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562199 | ||||||
chr4:83562199 | AATATATA others(29): Show |
A | 1 | a0001c0001t0003g0061 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.208+17599_208+1763 others(40): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562199 | ||||||
chr4:83562200 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.208+17598A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562200 | |||||||
chr4:83562204 | A | AT | 17 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0009 others(14): Show |
17 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.208+17603dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562204 | ||||||
chr4:83562204 | A | ATATAT | 8 | a0001c0001t0003g0197 a0001c0001t0004g0199 a0001c0001t0004g0200 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+17603_208+1760 others(9): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562204 | ||||||
chr4:83562210 | AT | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0021 a0001c0001t0002g0192 others(1): Show |
4 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+17610delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562210 | ||||||
chr4:83562211 | T | TA | 22 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0009 others(19): Show |
22 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.208+17609_208+1761 others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562211 | |||||||
chr4:83562211 | T | TTA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0035 others(3): Show |
6 | HG00639.hp2 HG00741.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+17622_208+1762 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562211 | ||||||
chr4:83562211 | T | TTATATAT others(27): Show |
1 | a0001c0001t0001g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208+17623_208+1762 others(38): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562211 | ||||||
chr4:83562211 | TTATATAT others(19): Show |
T | 1 | a0001c0001t0001g0158 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.208+17622_208+1764 others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562211 | ||||||
chr4:83562214 | T | TA | 19 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0009 others(16): Show |
19 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.208+17613dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | ||||||
chr4:83562214 | T | TATATA | 8 | a0001c0001t0003g0197 a0001c0001t0004g0199 a0001c0001t0004g0200 others(5): Show |
8 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+17613_208+1761 others(9): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | ||||||
chr4:83562214 | T | TATATATA others(2): Show |
88 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.208+17613_208+1762 others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | ||||||
chr4:83562214 | T | TATATATA others(24): Show |
1 | a0001c0001t0002g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.208+17621_208+1762 others(35): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | ||||||
chr4:83562214 | T | TATATATA others(24): Show |
3 | a0001c0001t0003g0183 a0001c0001t0005g0182 a0001c0001t0005g0184 |
3 | HG02258.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.208+17621_208+1762 others(35): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | ||||||
chr4:83562214 | T | TATATATA others(22): Show |
1 | a0001c0001t0003g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.208+17621_208+1762 others(33): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | ||||||
chr4:83562214 | T | TATATATA others(28): Show |
1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+17634_208+1763 others(39): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562214 | ||||||
chr4:83562224 | TA | T | 7 | a0001c0001t0001g0051 a0001c0001t0002g0007 a0001c0001t0002g0020 others(4): Show |
7 | HG00642.hp1 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+17624delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562224 | ||||||
chr4:83562225 | A | T | 3 | a0001c0001t0005g0196 a0001c0001t0005g0318 a0001c0001t0005g0333 |
3 | HG02896.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.208+17623A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562225 | |||||||
chr4:83562228 | AT | A | 4 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 others(1): Show |
4 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+17627delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562228 | |||||||
chr4:83562232 | A | G | 4 | a0001c0001t0003g0183 a0001c0001t0003g0194 a0001c0001t0005g0182 others(1): Show |
4 | HG02258.hp1 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+17630A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562232 | |||||||
chr4:83562235 | T | A | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.208+17633T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562235 | |||||||
chr4:83562235 | TA | T | 4 | a0001c0001t0001g0051 a0001c0001t0003g0016 a0001c0001t0003g0056 others(1): Show |
4 | HG00642.hp1 HG04228.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+17635delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562235 | ||||||
chr4:83562236 | A | AT | 65 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0064 others(62): Show |
66 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.208+17634_208+1763 others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562236 | |||||||
chr4:83562236 | A | T | 2 | a0001c0001t0001g0091 a0001c0001t0003g0061 |
2 | HG02738.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.208+17634A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562236 | |||||||
chr4:83562237 | A | T | 3 | a0001c0001t0005g0225 a0001c0001t0009g0186 a0001c0001t0009g0187 |
3 | HG03130.hp1 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.208+17635A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562237 | |||||||
chr4:83562238 | T | A | 21 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG01243.hp1 HG02486.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.208+17636T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562238 | |||||||
chr4:83562248 | T | A | 2 | a0001c0001t0003g0006 a0001c0001t0003g0175 |
2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.208+17646T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562248 | |||||||
chr4:83562775 | C | G | 1 | a0001c0001t0002g0322 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.208+18173C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562775 | |||||||
chr4:83562791 | G | GAGAT | 5 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+18191_208+1819 others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562791 | ||||||
chr4:83562795 | T | TATAG | 36 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0332 others(33): Show |
36 | HG00099.hp1 HG01243.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.208+18215_208+1821 others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562795 | ||||||
chr4:83562795 | T | TATAGACA others(13): Show |
5 | a0001c0001t0005g0198 a0001c0001t0006g0212 a0001c0001t0007g0188 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+18198_208+1819 others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562795 | ||||||
chr4:83562795 | T | TATAGATA others(1): Show |
63 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(60): Show |
64 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.208+18211_208+1821 others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562795 | ||||||
chr4:83562795 | T | TATAGATA others(5): Show |
2 | a0001c0001t0003g0036 a0001c0001t0003g0321 |
2 | HG04184.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.208+18207_208+1821 others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562795 | ||||||
chr4:83562795 | T | TATAGATA others(9): Show |
1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.208+18203_208+1821 others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83562795 | ||||||
chr4:83562877 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.208+18275G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562877 | |||||||
chr4:83562881 | G | T | 3 | a0001c0001t0007g0188 a0001c0001t0007g0189 a0001c0001t0007g0190 |
3 | HG02622.hp2 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.208+18279G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562881 | |||||||
chr4:83562963 | G | A | 75 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(72): Show |
76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.208+18361G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562963 | |||||||
chr4:83562967 | T | G | 75 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(72): Show |
76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.208+18365T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83562967 | |||||||
chr4:83563180 | G | A | 75 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(72): Show |
76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.209-18382G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563180 | |||||||
chr4:83563478 | C | CT | 7 | a0001c0001t0001g0093 a0001c0001t0001g0124 a0001c0001t0001g0173 others(4): Show |
7 | HG00438.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-18063dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83563478 | ||||||
chr4:83563478 | CT | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.209-18063delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83563478 | ||||||
chr4:83563478 | CTT | C | 7 | a0001c0001t0003g0006 a0001c0001t0003g0015 a0001c0001t0003g0016 others(4): Show |
7 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-18064_209-1806 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83563478 | ||||||
chr4:83563481 | T | C | 7 | a0001c0001t0003g0183 a0001c0001t0003g0194 a0001c0001t0005g0182 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-18081T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563481 | |||||||
chr4:83563696 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.209-17866G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563696 | |||||||
chr4:83563728 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.209-17834G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563728 | |||||||
chr4:83563773 | A | G | 75 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(72): Show |
76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.209-17789A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83563773 | |||||||
chr4:83564062 | G | A | 5 | a0001c0001t0005g0198 a0001c0001t0006g0212 a0001c0001t0007g0188 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-17500G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564062 | |||||||
chr4:83564247 | G | A | 28 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(25): Show |
28 | HG00099.hp1 HG01243.hp1 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.209-17315G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564247 | |||||||
chr4:83564374 | C | T | 18 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(15): Show |
18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-17188C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564374 | |||||||
chr4:83564469 | C | T | 3 | a0001c0001t0001g0097 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.209-17093C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564469 | |||||||
chr4:83564537 | A | G | 10 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(7): Show |
10 | HG00099.hp1 HG02486.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-17025A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564537 | |||||||
chr4:83564557 | G | A | 2 | a0001c0001t0006g0002 a0001c0001t0006g0003 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.209-17005G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564557 | |||||||
chr4:83564596 | A | G | 18 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(15): Show |
18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-16966A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564596 | |||||||
chr4:83564655 | C | T | 18 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(15): Show |
18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-16907C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564655 | |||||||
chr4:83564685 | C | A | 81 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0027 others(78): Show |
81 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.209-16877C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564685 | |||||||
chr4:83564706 | G | GA | 18 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(15): Show |
18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-16847dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83564706 | ||||||
chr4:83564866 | T | A | 1 | a0001c0001t0003g0237 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.209-16696T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564866 | |||||||
chr4:83564878 | A | AT | 18 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(15): Show |
18 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-16676dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83564878 | ||||||
chr4:83564967 | A | G | 7 | a0001c0001t0003g0197 a0001c0001t0004g0199 a0001c0001t0004g0200 others(4): Show |
7 | HG01243.hp2 HG02055.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-16595A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83564967 | |||||||
chr4:83565011 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(67): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-16551C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565011 | |||||||
chr4:83565012 | G | A | 3 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0206 |
3 | HG01891.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.209-16550G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565012 | |||||||
chr4:83565161 | C | T | 14 | a0001c0001t0001g0093 a0001c0001t0002g0219 a0001c0001t0002g0220 others(11): Show |
14 | HG01243.hp1 HG02109.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.209-16401C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565161 | |||||||
chr4:83565213 | G | T | 1 | a0001c0001t0004g0147 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.209-16349G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565213 | |||||||
chr4:83565341 | T | A | 1 | a0001c0001t0002g0315 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.209-16221T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565341 | |||||||
chr4:83565479 | A | G | 3 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0206 |
3 | HG01891.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.209-16083A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565479 | |||||||
chr4:83565495 | AT | A | 96 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(93): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.209-16058delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83565495 | ||||||
chr4:83565530 | G | A | 96 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(93): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.209-16032G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565530 | |||||||
chr4:83565585 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.209-15977G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565585 | |||||||
chr4:83565685 | C | T | 3 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 |
3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.209-15877C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565685 | |||||||
chr4:83565705 | C | T | 2 | a0001c0001t0003g0183 a0001c0001t0005g0182 |
2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.209-15857C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565705 | |||||||
chr4:83565715 | G | A | 88 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(85): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.209-15847G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565715 | |||||||
chr4:83565776 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(67): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-15786C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565776 | |||||||
chr4:83565782 | G | A | 28 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(25): Show |
28 | HG00099.hp1 HG01243.hp1 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.209-15780G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565782 | |||||||
chr4:83565936 | G | A | 2 | a0002c0002t0003g0145 a0002c0002t0003g0146 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.209-15626G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565936 | |||||||
chr4:83565951 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.209-15611C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83565951 | |||||||
chr4:83566066 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.209-15496C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566066 | |||||||
chr4:83566217 | T | C | 2 | a0001c0001t0002g0332 a0001c0001t0006g0206 |
2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.209-15345T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566217 | |||||||
chr4:83566264 | C | G | 1 | a0001c0001t0003g0006 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.209-15298C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566264 | |||||||
chr4:83566308 | G | A | 1 | a0001c0001t0005g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.209-15254G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566308 | |||||||
chr4:83566393 | A | C | 1 | a0001c0001t0002g0098 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.209-15169A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566393 | |||||||
chr4:83566404 | T | A | 113 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.209-15158T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566404 | |||||||
chr4:83566408 | AAATT | A | 3 | a0001c0001t0007g0188 a0001c0001t0007g0189 a0001c0001t0007g0190 |
3 | HG02622.hp2 HG03225.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.209-15145_209-1514 others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566408 | ||||||
chr4:83566419 | T | TTTA | 115 | a0001c0001t0001g0087 a0001c0001t0001g0106 a0001c0001t0001g0107 others(112): Show |
115 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.209-15116_209-1511 others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566419 | ||||||
chr4:83566419 | T | TTTATTA | 64 | a0001c0001t0001g0050 a0001c0001t0003g0001 a0001c0001t0003g0005 others(61): Show |
65 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.209-15119_209-1511 others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566419 | ||||||
chr4:83566419 | T | TTTATTAT others(2): Show |
15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0064 others(12): Show |
15 | HG00099.hp1 HG01243.hp1 NA18946.hp1 others(12): Show |
intron_variant | MODIFIER | c.209-15122_209-1511 others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566419 | ||||||
chr4:83566419 | T | TTTATTAT others(5): Show |
4 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0309 others(1): Show |
4 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-15125_209-1511 others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566419 | ||||||
chr4:83566419 | T | TTTATTAT others(8): Show |
9 | a0001c0001t0004g0013 a0001c0001t0004g0221 a0001c0001t0005g0014 others(6): Show |
9 | HG02630.hp2 HG02809.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-15128_209-1511 others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83566419 | ||||||
chr4:83566970 | T | C | 98 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(95): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.209-14592T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83566970 | |||||||
chr4:83567146 | AT | A | 13 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0013 others(10): Show |
13 | HG01243.hp1 HG02630.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-14408delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83567146 | ||||||
chr4:83567229 | T | C | 94 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(91): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.209-14333T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83567229 | |||||||
chr4:83567370 | G | A | 24 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(21): Show |
24 | HG00099.hp1 HG01243.hp1 HG02486.hp2 others(21): Show |
intron_variant | MODIFIER | c.209-14192G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83567370 | |||||||
chr4:83567531 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.209-14031G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83567531 | |||||||
chr4:83567818 | G | A | 1 | a0001c0001t0004g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.209-13744G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83567818 | |||||||
chr4:83567969 | C | T | 94 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(91): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.209-13593C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83567969 | |||||||
chr4:83568316 | A | G | 4 | a0001c0001t0003g0183 a0001c0001t0003g0194 a0001c0001t0004g0309 others(1): Show |
4 | HG02109.hp1 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-13246A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568316 | |||||||
chr4:83568318 | G | A | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-13244G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568318 | |||||||
chr4:83568358 | G | A | 1 | a0001c0001t0004g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.209-13204G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568358 | |||||||
chr4:83568364 | C | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0132 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.209-13198C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568364 | |||||||
chr4:83568493 | C | T | 94 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(91): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.209-13069C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568493 | |||||||
chr4:83568510 | CT | C | 26 | a0001c0001t0001g0090 a0001c0001t0002g0007 a0001c0001t0002g0020 others(23): Show |
26 | HG00099.hp1 HG00642.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.209-13037delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83568510 | ||||||
chr4:83568569 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.209-12993G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568569 | |||||||
chr4:83568594 | G | C | 1 | a0001c0001t0002g0249 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.209-12968G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568594 | |||||||
chr4:83568634 | G | A | 92 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(89): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.209-12928G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568634 | |||||||
chr4:83568639 | C | G | 1 | a0001c0001t0001g0121 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.209-12923C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568639 | |||||||
chr4:83568653 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.209-12909A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83568653 | |||||||
chr4:83569037 | C | A | 80 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(77): Show |
81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.209-12525C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569037 | |||||||
chr4:83569195 | A | G | 70 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(67): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-12367A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569195 | |||||||
chr4:83569371 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.209-12191G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569371 | |||||||
chr4:83569544 | ATGTC | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(67): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-12017_209-1201 others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569544 | |||||||
chr4:83569555 | G | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(67): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-12007G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569555 | |||||||
chr4:83569586 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.209-11976A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569586 | |||||||
chr4:83569670 | G | A | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.209-11892G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569670 | |||||||
chr4:83569838 | T | TA | 7 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(4): Show |
7 | HG01257.hp2 HG01258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-11714dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83569838 | ||||||
chr4:83569859 | T | A | 80 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(77): Show |
81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.209-11703T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569859 | |||||||
chr4:83569887 | C | T | 8 | a0001c0001t0005g0198 a0001c0001t0006g0002 a0001c0001t0006g0003 others(5): Show |
8 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-11675C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569887 | |||||||
chr4:83569968 | A | C | 115 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(112): Show |
116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.209-11594A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83569968 | |||||||
chr4:83570154 | C | T | 70 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(67): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.209-11408C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570154 | |||||||
chr4:83570265 | T | G | 9 | a0001c0001t0002g0332 a0001c0001t0005g0198 a0001c0001t0006g0002 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-11297T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570265 | |||||||
chr4:83570471 | C | CT | 34 | a0001c0001t0001g0089 a0001c0001t0001g0158 a0001c0001t0001g0193 others(31): Show |
34 | HG01243.hp1 HG02055.hp1 HG02071.hp2 others(31): Show |
intron_variant | MODIFIER | c.209-11072dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83570471 | ||||||
chr4:83570471 | CT | C | 77 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(74): Show |
78 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.209-11072delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83570471 | ||||||
chr4:83570527 | C | G | 9 | a0001c0001t0002g0332 a0001c0001t0005g0198 a0001c0001t0006g0002 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-11035C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570527 | |||||||
chr4:83570563 | C | A | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-10999C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570563 | |||||||
chr4:83570621 | C | T | 6 | a0001c0001t0001g0076 a0001c0001t0001g0090 a0001c0001t0001g0097 others(3): Show |
6 | HG02698.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-10941C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570621 | |||||||
chr4:83570910 | A | G | 1 | a0001c0001t0005g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.209-10652A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570910 | |||||||
chr4:83570967 | C | A | 17 | a0001c0001t0002g0208 a0001c0001t0004g0013 a0001c0001t0004g0306 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.209-10595C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83570967 | |||||||
chr4:83571061 | T | C | 3 | a0001c0001t0005g0182 a0001c0001t0005g0205 a0001c0001t0005g0225 |
3 | HG00099.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.209-10501T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571061 | |||||||
chr4:83571438 | CT | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-10120delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83571438 | ||||||
chr4:83571458 | T | TTTGTGGG others(7): Show |
1 | a0001c0001t0001g0034 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.209-10102_209-1008 others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83571458 | ||||||
chr4:83571506 | TAAGTATT others(22): Show |
T | 1 | a0001c0001t0001g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.209-10053_209-1002 others(33): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83571506 | ||||||
chr4:83571585 | A | T | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-9977A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571585 | |||||||
chr4:83571680 | A | G | 5 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-9882A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571680 | |||||||
chr4:83571687 | TATATATA others(13): Show |
T | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9865_209-9846d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83571687 | ||||||
chr4:83571715 | T | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9847T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571715 | |||||||
chr4:83571719 | C | CACACATA others(35): Show |
1 | a0001c0001t0001g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209-9831_209-9790d others(44): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83571719 | ||||||
chr4:83571725 | T | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9837T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571725 | |||||||
chr4:83571739 | C | T | 1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.209-9823C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571739 | |||||||
chr4:83571740 | G | A | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9822G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571740 | |||||||
chr4:83571768 | A | G | 2 | a0001c0001t0002g0029 a0001c0001t0002g0265 |
2 | NA18612.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.209-9794A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571768 | |||||||
chr4:83571901 | T | A | 1 | a0001c0001t0002g0264 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.209-9661T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571901 | |||||||
chr4:83571922 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.209-9640G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571922 | |||||||
chr4:83571952 | T | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9610T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571952 | |||||||
chr4:83571973 | A | G | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9589A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83571973 | |||||||
chr4:83572051 | A | T | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209-9511A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572051 | |||||||
chr4:83572160 | A | G | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9402A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572160 | |||||||
chr4:83572469 | C | T | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-9093C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572469 | |||||||
chr4:83572475 | T | G | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9087T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572475 | |||||||
chr4:83572477 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9085C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572477 | |||||||
chr4:83572478 | T | G | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9084T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572478 | |||||||
chr4:83572479 | T | C | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9083T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572479 | |||||||
chr4:83572485 | T | G | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9077T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572485 | |||||||
chr4:83572487 | A | T | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9075A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572487 | |||||||
chr4:83572490 | T | G | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9072T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572490 | |||||||
chr4:83572498 | T | G | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9064T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572498 | |||||||
chr4:83572513 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9049C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572513 | |||||||
chr4:83572514 | A | C | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9048A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572514 | |||||||
chr4:83572518 | A | T | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-9044A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572518 | |||||||
chr4:83572533 | A | C | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209-9029A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572533 | |||||||
chr4:83572845 | C | T | 13 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0003g0197 others(10): Show |
13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-8717C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572845 | |||||||
chr4:83572846 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.209-8716G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83572846 | |||||||
chr4:83573012 | CAT | C | 7 | a0001c0001t0001g0144 a0001c0001t0002g0210 a0001c0001t0002g0213 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-8547_209-8546d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83573012 | ||||||
chr4:83573080 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.209-8482G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83573080 | |||||||
chr4:83573169 | C | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0149 others(2): Show |
5 | HG02451.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-8393C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83573169 | |||||||
chr4:83573284 | GCTTGCCA others(7): Show |
G | 1 | a0001c0001t0001g0096 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.209-8277_209-8264d others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83573284 | |||||||
chr4:83573773 | T | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-7789T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83573773 | |||||||
chr4:83574220 | G | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-7342G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574220 | |||||||
chr4:83574366 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.209-7196T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574366 | |||||||
chr4:83574484 | G | A | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209-7078G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574484 | |||||||
chr4:83574489 | T | C | 86 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(83): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.209-7073T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574489 | |||||||
chr4:83574496 | T | TAGAG | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-7063_209-7062i others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574496 | ||||||
chr4:83574574 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.209-6988C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574574 | |||||||
chr4:83574603 | C | G | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-6959C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574603 | |||||||
chr4:83574624 | A | AT | 9 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0127 others(6): Show |
9 | HG02071.hp1 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-6885dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | A | ATT | 13 | a0001c0001t0001g0101 a0001c0001t0001g0121 a0001c0001t0001g0168 others(10): Show |
13 | HG00408.hp2 HG00597.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-6886_209-6885d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | A | ATTT | 6 | a0001c0001t0001g0079 a0001c0001t0001g0167 a0001c0001t0003g0037 others(3): Show |
6 | HG02602.hp2 HG02895.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-6887_209-6885d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0003g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.209-6897_209-6885d others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0002g0329 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.209-6902_209-6885d others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | AT | A | 9 | a0001c0001t0001g0080 a0001c0001t0001g0144 a0001c0001t0002g0213 others(6): Show |
9 | HG01884.hp2 HG02809.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-6885delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATT | A | 13 | a0001c0001t0001g0050 a0001c0001t0001g0152 a0001c0001t0003g0036 others(10): Show |
13 | HG00609.hp1 HG01109.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-6886_209-6885d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTT | A | 12 | a0001c0001t0001g0066 a0001c0001t0003g0001 a0001c0001t0003g0040 others(9): Show |
13 | HG00280.hp2 HG02004.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-6887_209-6885d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0162 |
2 | HG02257.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.209-6894_209-6885d others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0307 a0001c0001t0002g0280 others(1): Show |
4 | HG01261.hp2 HG03927.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-6895_209-6885d others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0035 a0001c0001t0004g0306 |
2 | HG01243.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.209-6896_209-6885d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(6): Show |
A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0112 a0001c0001t0001g0130 others(6): Show |
9 | HG01169.hp1 HG01433.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-6897_209-6885d others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(7): Show |
A | 10 | a0001c0001t0001g0077 a0001c0001t0001g0111 a0001c0001t0001g0123 others(7): Show |
10 | HG01168.hp1 HG02071.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-6898_209-6885d others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(8): Show |
A | 12 | a0001c0001t0001g0023 a0001c0001t0001g0087 a0001c0001t0001g0093 others(9): Show |
12 | HG00741.hp2 HG02109.hp2 HG03209.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-6899_209-6885d others(17): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(9): Show |
A | 10 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(7): Show |
10 | HG00597.hp2 HG01515.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-6900_209-6885d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(10): Show |
A | 12 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0097 others(9): Show |
12 | HG02486.hp2 HG02970.hp2 HG03492.hp2 others(9): Show |
intron_variant | MODIFIER | c.209-6901_209-6885d others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(11): Show |
A | 7 | a0001c0001t0001g0128 a0001c0001t0002g0020 a0001c0001t0002g0021 others(4): Show |
7 | HG00733.hp1 HG02293.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-6902_209-6885d others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(12): Show |
A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0091 a0001c0001t0002g0292 others(9): Show |
12 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-6903_209-6885d others(21): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(13): Show |
A | 8 | a0001c0001t0002g0316 a0001c0001t0003g0006 a0001c0001t0003g0018 others(5): Show |
8 | HG00140.hp2 HG01168.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-6904_209-6885d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(14): Show |
A | 12 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0003g0015 others(9): Show |
12 | HG00642.hp1 HG00741.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.209-6905_209-6885d others(23): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(15): Show |
A | 13 | a0001c0001t0001g0156 a0001c0001t0002g0228 a0001c0001t0002g0229 others(10): Show |
13 | HG01169.hp2 HG02056.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-6906_209-6885d others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(16): Show |
A | 6 | a0001c0001t0001g0104 a0001c0001t0002g0231 a0001c0001t0002g0252 others(3): Show |
6 | HG01257.hp1 HG01981.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-6907_209-6885d others(25): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(17): Show |
A | 7 | a0001c0001t0003g0005 a0001c0001t0003g0038 a0001c0001t0004g0147 others(4): Show |
7 | HG00099.hp1 HG00733.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-6908_209-6885d others(26): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(18): Show |
A | 5 | a0001c0001t0001g0151 a0001c0001t0004g0200 a0001c0001t0005g0004 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-6909_209-6885d others(27): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(19): Show |
A | 12 | a0001c0001t0002g0098 a0001c0001t0002g0332 a0001c0001t0004g0199 others(9): Show |
12 | HG01106.hp2 HG01243.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-6910_209-6885d others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(20): Show |
A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0134 a0001c0001t0002g0246 others(6): Show |
9 | HG02027.hp2 NA18951.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-6911_209-6885d others(29): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(21): Show |
A | 46 | a0001c0001t0001g0092 a0001c0001t0001g0103 a0001c0001t0001g0236 others(43): Show |
46 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.209-6912_209-6885d others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(22): Show |
A | 8 | a0001c0001t0001g0124 a0001c0001t0001g0240 a0001c0001t0002g0259 others(5): Show |
8 | HG01256.hp2 NA18939.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-6913_209-6885d others(31): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(23): Show |
A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0142 a0001c0001t0002g0281 |
3 | HG01081.hp1 HG02015.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.209-6914_209-6885d others(32): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(24): Show |
A | 13 | a0001c0001t0001g0027 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG02055.hp1 HG02809.hp1 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-6915_209-6885d others(33): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(25): Show |
A | 9 | a0001c0001t0001g0070 a0001c0001t0001g0086 a0001c0001t0001g0089 others(6): Show |
9 | HG00438.hp1 HG00609.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-6916_209-6885d others(34): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574624 | ATTTTTTT others(26): Show |
A | 2 | a0001c0001t0002g0325 a0001c0001t0008g0102 |
2 | NA18956.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.209-6917_209-6885d others(35): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574624 | ||||||
chr4:83574665 | TTTTTTTT others(6): Show |
T | 1 | a0001c0001t0001g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.209-6896_209-6884d others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574665 | |||||||
chr4:83574779 | G | A | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-6783G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574779 | |||||||
chr4:83574880 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6682T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574880 | |||||||
chr4:83574881 | T | G | 16 | a0001c0001t0002g0208 a0001c0001t0004g0013 a0001c0001t0004g0306 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-6681T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574881 | |||||||
chr4:83574881 | T | TTG | 68 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(65): Show |
69 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.209-6681_209-6680i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574881 | |||||||
chr4:83574882 | G | GT | 22 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0001g0156 others(19): Show |
22 | HG00099.hp1 HG00639.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.209-6667dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83574882 | ||||||
chr4:83574882 | G | T | 89 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(86): Show |
90 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.209-6680G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574882 | |||||||
chr4:83574944 | C | T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-6618C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83574944 | |||||||
chr4:83575065 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.209-6497G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575065 | |||||||
chr4:83575129 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6433G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575129 | |||||||
chr4:83575130 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6432C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575130 | |||||||
chr4:83575131 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6431C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575131 | |||||||
chr4:83575132 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6430T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575132 | |||||||
chr4:83575133 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.209-6429C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575133 | |||||||
chr4:83575191 | A | G | 90 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(87): Show |
91 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.209-6371A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575191 | |||||||
chr4:83575511 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.209-6051C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575511 | |||||||
chr4:83575517 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.209-6045A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575517 | |||||||
chr4:83575700 | C | T | 8 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(5): Show |
8 | HG02258.hp2 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-5862C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575700 | |||||||
chr4:83575998 | C | A | 11 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-5564C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83575998 | |||||||
chr4:83576323 | G | A | 3 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 |
3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.209-5239G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83576323 | |||||||
chr4:83576412 | T | TTTTA | 131 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0035 others(128): Show |
131 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.209-5109_209-5106d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83576412 | ||||||
chr4:83576412 | T | TTTTATTT others(1): Show |
19 | a0001c0001t0001g0173 a0001c0001t0002g0010 a0001c0001t0002g0219 others(16): Show |
19 | HG01070.hp2 HG01891.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.209-5113_209-5106d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83576412 | ||||||
chr4:83576412 | TTTTA | T | 14 | a0001c0001t0001g0092 a0001c0001t0001g0106 a0001c0001t0001g0107 others(11): Show |
14 | HG00140.hp2 HG00280.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.209-5109_209-5106d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83576412 | ||||||
chr4:83576412 | TTTTATTT others(5): Show |
T | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209-5117_209-5106d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83576412 | ||||||
chr4:83576471 | T | A | 1 | a0001c0001t0007g0188 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.209-5091T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83576471 | |||||||
chr4:83576472 | C | T | 1 | a0001c0001t0007g0188 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.209-5090C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83576472 | |||||||
chr4:83576766 | A | T | 1 | a0001c0001t0001g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.209-4796A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83576766 | |||||||
chr4:83576896 | G | C | 1 | a0001c0001t0002g0215 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.209-4666G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83576896 | |||||||
chr4:83577010 | T | G | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.209-4552T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577010 | |||||||
chr4:83577066 | T | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-4496T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577066 | |||||||
chr4:83577195 | T | A | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-4367T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577195 | |||||||
chr4:83577205 | G | GAAAGACA others(317): Show |
3 | a0001c0001t0003g0044 a0001c0001t0003g0045 a0001c0001t0003g0046 |
3 | NA18612.hp1 NA18969.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.209-4346_209-4345i others(326): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577205 | ||||||
chr4:83577441 | A | G | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-4121A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577441 | |||||||
chr4:83577788 | C | CT | 59 | a0001c0001t0001g0027 a0001c0001t0001g0086 a0001c0001t0001g0087 others(56): Show |
59 | HG00099.hp1 HG00099.hp2 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.209-3748dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | ||||||
chr4:83577788 | C | CTT | 13 | a0001c0001t0001g0093 a0001c0001t0001g0101 a0001c0001t0002g0219 others(10): Show |
13 | HG00408.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-3749_209-3748d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | ||||||
chr4:83577788 | C | CTTT | 54 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0035 others(51): Show |
55 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.209-3750_209-3748d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | ||||||
chr4:83577788 | C | CTTTT | 17 | a0001c0001t0003g0016 a0001c0001t0003g0025 a0001c0001t0003g0026 others(14): Show |
17 | HG00280.hp2 HG00642.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.209-3751_209-3748d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | ||||||
chr4:83577788 | C | CTTTTT | 6 | a0001c0001t0003g0045 a0001c0001t0003g0053 a0001c0001t0003g0175 others(3): Show |
6 | HG01258.hp2 HG03831.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-3752_209-3748d others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | ||||||
chr4:83577788 | CT | C | 6 | a0001c0001t0001g0097 a0001c0001t0001g0142 a0001c0001t0002g0213 others(3): Show |
6 | HG01081.hp1 HG02897.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-3748delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83577788 | ||||||
chr4:83577937 | TTACAGGC others(53): Show |
T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-3624_209-3565d others(62): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577937 | |||||||
chr4:83577951 | C | T | 13 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0003g0197 others(10): Show |
13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-3611C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577951 | |||||||
chr4:83577976 | T | C | 20 | a0001c0001t0002g0208 a0001c0001t0003g0183 a0001c0001t0003g0194 others(17): Show |
20 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.209-3586T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83577976 | |||||||
chr4:83578231 | T | C | 3 | a0001c0001t0003g0081 a0001c0001t0003g0175 a0001c0001t0003g0218 |
3 | HG00280.hp2 HG01081.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.209-3331T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578231 | |||||||
chr4:83578376 | T | C | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | HG01109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.209-3186T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578376 | |||||||
chr4:83578829 | A | C | 3 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 |
3 | HG02145.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.209-2733A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578829 | |||||||
chr4:83578857 | T | TTTCC | 75 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(72): Show |
76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.209-2688_209-2685d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578857 | ||||||
chr4:83578857 | T | TTTCCTTC others(1): Show |
9 | a0001c0001t0003g0183 a0001c0001t0003g0194 a0001c0001t0005g0014 others(6): Show |
9 | HG02055.hp1 HG02258.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2692_209-2685d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578857 | ||||||
chr4:83578921 | T | C | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2641T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578921 | |||||||
chr4:83578922 | T | TTTCTTTC others(4): Show |
57 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0066 others(54): Show |
58 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.209-2637_209-2627d others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578922 | ||||||
chr4:83578930 | T | TTTC | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0003g0006 others(13): Show |
16 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-2629_209-2627d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578930 | ||||||
chr4:83578933 | C | CT | 3 | a0001c0001t0001g0097 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.209-2626dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578933 | ||||||
chr4:83578933 | CTTTCT | C | 7 | a0001c0001t0004g0031 a0001c0001t0004g0147 a0001c0001t0004g0201 others(4): Show |
7 | HG02055.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-2611_209-2607d others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578933 | ||||||
chr4:83578937 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.209-2625C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578937 | |||||||
chr4:83578937 | CT | C | 3 | a0001c0001t0005g0012 a0001c0001t0005g0207 a0001c0001t0005g0211 |
3 | HG03139.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.209-2621delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578937 | ||||||
chr4:83578938 | T | TTTC | 16 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0003g0006 others(13): Show |
16 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-2622_209-2621i others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578938 | ||||||
chr4:83578939 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.209-2623T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578939 | |||||||
chr4:83578942 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.209-2620C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578942 | |||||||
chr4:83578943 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0002g0313 |
2 | NA18952.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.209-2619T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578943 | |||||||
chr4:83578943 | T | TTCTTTCT others(3): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0148 |
2 | HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.209-2618_209-2617i others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578943 | ||||||
chr4:83578943 | T | TTTCTTTC others(4): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.209-2617_209-2616i others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578943 | ||||||
chr4:83578943 | TTTTCTTT others(68): Show |
T | 1 | a0001c0001t0005g0225 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.209-2611_209-2537d others(77): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578943 | ||||||
chr4:83578943 | TTTTCTTT others(76): Show |
T | 1 | a0001c0001t0009g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.209-2611_209-2529d others(85): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578943 | ||||||
chr4:83578946 | TCTTTTCT others(64): Show |
T | 1 | a0001c0001t0009g0186 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.209-2611_209-2541d others(73): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578946 | ||||||
chr4:83578947 | CT | C | 23 | a0001c0001t0001g0091 a0001c0001t0001g0099 a0001c0001t0001g0116 others(20): Show |
23 | HG01243.hp1 HG01243.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.209-2611delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578947 | ||||||
chr4:83578947 | CTTT | C | 13 | a0001c0001t0001g0307 a0001c0001t0002g0214 a0001c0001t0002g0228 others(10): Show |
13 | HG02258.hp2 HG02559.hp2 HG02970.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-2613_209-2611d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578947 | ||||||
chr4:83578947 | CTTTTCTT | C | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0002g0233 |
3 | HG02622.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.209-2613_209-2607d others(9): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578947 | ||||||
chr4:83578947 | CTTTTCTT others(4): Show |
C | 1 | a0001c0001t0002g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.209-2613_209-2603d others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578947 | ||||||
chr4:83578948 | T | TC | 97 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0066 others(94): Show |
98 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.209-2614_209-2613i others(3): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | |||||||
chr4:83578948 | T | TCTTTC | 25 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0049 others(22): Show |
25 | HG01168.hp2 HG01192.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.209-2614_209-2613i others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | |||||||
chr4:83578948 | T | TCTTTCTT others(2): Show |
24 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(21): Show |
24 | HG00408.hp1 HG00438.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.209-2614_209-2613i others(11): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | |||||||
chr4:83578948 | T | TCTTTCTT others(6): Show |
6 | a0001c0001t0003g0038 a0001c0001t0003g0040 a0001c0001t0003g0041 others(3): Show |
6 | HG00597.hp1 HG02015.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2614_209-2613i others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | |||||||
chr4:83578948 | T | TCTTTCTT others(10): Show |
1 | a0001c0001t0003g0043 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.209-2614_209-2613i others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | |||||||
chr4:83578948 | T | TCTTTCTT others(22): Show |
1 | a0001c0001t0003g0138 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.209-2614_209-2613i others(31): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578948 | |||||||
chr4:83578948 | T | TTCTTTCT others(19): Show |
1 | a0001c0001t0003g0071 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.209-2613_209-2612i others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | ||||||
chr4:83578948 | T | TTTC | 30 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0023 others(27): Show |
30 | HG00609.hp2 HG00741.hp2 HG01515.hp2 others(27): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | ||||||
chr4:83578948 | T | TTTCTTTC | 14 | a0001c0001t0001g0085 a0001c0001t0001g0104 a0001c0001t0001g0106 others(11): Show |
14 | HG00597.hp2 HG01106.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(9): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | ||||||
chr4:83578948 | T | TTTCTTTC others(4): Show |
12 | a0001c0001t0001g0077 a0001c0001t0001g0083 a0001c0001t0001g0118 others(9): Show |
12 | HG01168.hp1 HG01175.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | ||||||
chr4:83578948 | T | TTTCTTTC others(8): Show |
16 | a0001c0001t0001g0090 a0001c0001t0001g0093 a0001c0001t0001g0096 others(13): Show |
16 | HG00408.hp2 HG01346.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(17): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | ||||||
chr4:83578948 | T | TTTCTTTC others(12): Show |
17 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0092 others(14): Show |
17 | HG01081.hp1 HG01261.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(21): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | ||||||
chr4:83578948 | T | TTTCTTTC others(16): Show |
8 | a0001c0001t0001g0034 a0001c0001t0001g0076 a0001c0001t0001g0095 others(5): Show |
8 | HG00438.hp1 HG02523.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2612_209-2611i others(25): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | ||||||
chr4:83578948 | T | TTTCTTTC others(20): Show |
3 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0132 |
3 | HG01169.hp1 NA18972.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.209-2612_209-2611i others(29): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | ||||||
chr4:83578948 | T | TTTCTTTC others(28): Show |
1 | a0001c0001t0001g0119 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.209-2612_209-2611i others(37): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578948 | ||||||
chr4:83578949 | T | C | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-2613T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578949 | |||||||
chr4:83578950 | T | TTC | 11 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0003g0006 others(8): Show |
11 | HG00642.hp1 HG01070.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-2610_209-2609d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578950 | ||||||
chr4:83578950 | TTCTTTCT others(60): Show |
T | 2 | a0001c0001t0005g0182 a0001c0001t0005g0205 |
2 | HG00099.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.209-2611_209-2545d others(69): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578950 | |||||||
chr4:83578952 | CTT | C | 5 | a0001c0001t0003g0026 a0001c0001t0003g0047 a0001c0001t0003g0048 others(2): Show |
5 | HG00280.hp2 HG01109.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2608_209-2607d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578952 | ||||||
chr4:83578958 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.209-2604T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578958 | |||||||
chr4:83578963 | T | G | 5 | a0001c0001t0005g0198 a0001c0001t0006g0002 a0001c0001t0006g0003 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2599T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578963 | |||||||
chr4:83578963 | T | TCTTGCTT others(51): Show |
3 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 |
3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.209-2596_209-2595i others(60): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578963 | ||||||
chr4:83578967 | T | G | 1 | a0001c0001t0003g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.209-2595T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578967 | |||||||
chr4:83578971 | T | G | 5 | a0001c0001t0002g0332 a0001c0001t0005g0004 a0001c0001t0006g0212 others(2): Show |
5 | HG02615.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-2591T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578971 | |||||||
chr4:83578978 | T | A | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2584T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578978 | |||||||
chr4:83578985 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0168 |
2 | HG01081.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.209-2577T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578985 | |||||||
chr4:83578987 | TCCTTCCT others(23): Show |
T | 3 | a0001c0001t0002g0208 a0001c0001t0005g0207 a0001c0001t0005g0211 |
3 | HG02559.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.209-2573_209-2544d others(32): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578987 | ||||||
chr4:83578989 | C | T | 192 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0070 others(189): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.209-2573C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578989 | |||||||
chr4:83578991 | TCCTTCCT others(19): Show |
T | 1 | a0001c0001t0005g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.209-2569_209-2544d others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578991 | ||||||
chr4:83578992 | C | T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2570C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578992 | |||||||
chr4:83578993 | C | T | 125 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0070 others(122): Show |
125 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.209-2569C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578993 | |||||||
chr4:83578995 | TCCTTCCT others(15): Show |
T | 7 | a0001c0001t0002g0247 a0001c0001t0002g0256 a0001c0001t0002g0257 others(4): Show |
7 | HG02004.hp2 HG02451.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-2565_209-2544d others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83578995 | ||||||
chr4:83578996 | C | T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2566C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578996 | |||||||
chr4:83578997 | C | T | 95 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0070 others(92): Show |
95 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.209-2565C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83578997 | |||||||
chr4:83579000 | C | T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2562C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579000 | |||||||
chr4:83579001 | C | T | 54 | a0001c0001t0001g0080 a0001c0001t0001g0148 a0001c0001t0001g0238 others(51): Show |
54 | HG00639.hp1 HG00642.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.209-2561C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579001 | |||||||
chr4:83579004 | C | T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2558C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579004 | |||||||
chr4:83579005 | C | T | 25 | a0001c0001t0001g0148 a0001c0001t0001g0307 a0001c0001t0002g0029 others(22): Show |
25 | HG01243.hp1 HG01346.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.209-2557C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579005 | |||||||
chr4:83579007 | TCCTTCTT others(3): Show |
T | 1 | a0001c0001t0002g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.209-2553_209-2544d others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579007 | ||||||
chr4:83579008 | C | T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2554C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579008 | |||||||
chr4:83579009 | C | T | 8 | a0001c0001t0001g0307 a0001c0001t0002g0214 a0001c0001t0002g0280 others(5): Show |
8 | HG01346.hp2 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2553C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579009 | |||||||
chr4:83579009 | CTTCTTTC others(29): Show |
C | 1 | a0001c0001t0012g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.209-2552_209-2517d others(38): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579009 | |||||||
chr4:83579009 | CTTCTTTC others(33): Show |
C | 1 | a0001c0001t0004g0306 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.209-2552_209-2513d others(42): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579009 | |||||||
chr4:83579009 | CTTCTTTC others(37): Show |
C | 2 | a0001c0001t0005g0318 a0001c0001t0014g0181 |
2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.209-2552_209-2509d others(46): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579009 | |||||||
chr4:83579012 | C | T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2550C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579012 | |||||||
chr4:83579013 | T | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0070 others(96): Show |
99 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.209-2549T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579013 | |||||||
chr4:83579017 | C | CCTTT | 9 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0001t0001g0128 others(6): Show |
9 | HG01106.hp2 HG01261.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.209-2485_209-2482d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579017 | C | CCTTTCTT others(1): Show |
4 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0124 others(1): Show |
4 | HG01891.hp2 NA18944.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-2489_209-2482d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579017 | C | CCTTTCTT others(5): Show |
3 | a0001c0001t0001g0114 a0001c0001t0001g0167 a0001c0001t0001g0176 |
3 | HG01175.hp2 HG03927.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.209-2493_209-2482d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579017 | C | CCTTTCTT others(13): Show |
1 | a0001c0001t0001g0110 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.209-2501_209-2482d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579017 | C | CTT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0077 others(19): Show |
22 | HG00597.hp2 HG00609.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.209-2545_209-2544i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | |||||||
chr4:83579017 | C | T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2545C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | |||||||
chr4:83579017 | CCT | C | 43 | a0001c0001t0001g0070 a0001c0001t0001g0079 a0001c0001t0001g0080 others(40): Show |
43 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.209-2544_209-2543d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | |||||||
chr4:83579017 | CCTTT | C | 29 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0035 others(26): Show |
29 | HG00639.hp2 HG00741.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.209-2485_209-2482d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579017 | CCTTTCT | C | 5 | a0001c0001t0002g0082 a0001c0001t0002g0214 a0001c0001t0002g0319 others(2): Show |
5 | HG00642.hp2 HG02559.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2544_209-2539d others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | |||||||
chr4:83579017 | CCTTTCTT others(1): Show |
C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0163 a0001c0001t0002g0332 others(1): Show |
4 | HG02040.hp2 HG02145.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-2489_209-2482d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579017 | CCTTTCTT others(3): Show |
C | 6 | a0001c0001t0002g0252 a0001c0001t0002g0261 a0001c0001t0002g0264 others(3): Show |
6 | HG00733.hp1 HG01257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2544_209-2535d others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | |||||||
chr4:83579017 | CCTTTCTT others(5): Show |
C | 1 | a0001c0001t0004g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2493_209-2482d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579017 | CCTTTCTT others(7): Show |
C | 8 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0002g0029 others(5): Show |
8 | HG01884.hp1 HG02145.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2544_209-2531d others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | |||||||
chr4:83579017 | CCTTTCTT others(9): Show |
C | 1 | a0001c0001t0004g0202 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.209-2497_209-2482d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579017 | CCTTTCTT others(11): Show |
C | 10 | a0001c0001t0001g0241 a0001c0001t0002g0010 a0001c0001t0002g0213 others(7): Show |
10 | HG00099.hp2 HG02717.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-2544_209-2527d others(20): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | |||||||
chr4:83579017 | CCTTTCTT others(13): Show |
C | 4 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(1): Show |
4 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2501_209-2482d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579017 | CCTTTCTT others(15): Show |
C | 9 | a0001c0001t0002g0270 a0001c0001t0002g0282 a0001c0001t0002g0294 others(6): Show |
9 | HG01192.hp1 HG02622.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2544_209-2523d others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | |||||||
chr4:83579017 | CCTTTCTT others(19): Show |
C | 3 | a0001c0001t0002g0249 a0001c0001t0002g0268 a0001c0001t0002g0275 |
3 | NA18968.hp2 NA18997.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.209-2544_209-2519d others(28): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579017 | |||||||
chr4:83579017 | CCTTTCTT others(25): Show |
C | 3 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0210 |
3 | HG02818.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.209-2513_209-2482d others(34): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579017 | CCTTTCTT others(29): Show |
C | 1 | a0001c0001t0005g0014 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.209-2517_209-2482d others(38): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579017 | ||||||
chr4:83579019 | T | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0077 others(20): Show |
23 | HG00597.hp2 HG00609.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.209-2543T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579019 | |||||||
chr4:83579021 | T | C | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2541T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579021 | |||||||
chr4:83579023 | T | C | 30 | a0001c0001t0001g0070 a0001c0001t0001g0079 a0001c0001t0001g0080 others(27): Show |
30 | HG00639.hp1 HG01070.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-2539T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579023 | |||||||
chr4:83579025 | T | TCC | 23 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0077 others(20): Show |
23 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.209-2536_209-2535i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579025 | ||||||
chr4:83579026 | CTT | C | 13 | a0001c0001t0001g0086 a0001c0001t0001g0091 a0001c0001t0001g0107 others(10): Show |
13 | HG00140.hp2 HG00642.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-2534_209-2533d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579026 | ||||||
chr4:83579027 | T | C | 19 | a0001c0001t0001g0080 a0001c0001t0001g0148 a0001c0001t0001g0307 others(16): Show |
19 | HG00642.hp2 HG01070.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.209-2535T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579027 | |||||||
chr4:83579029 | T | C | 14 | a0001c0001t0001g0086 a0001c0001t0001g0091 a0001c0001t0001g0107 others(11): Show |
14 | HG00140.hp2 HG00642.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.209-2533T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579029 | |||||||
chr4:83579029 | T | TCC | 9 | a0001c0001t0001g0070 a0001c0001t0001g0079 a0001c0001t0001g0133 others(6): Show |
9 | HG00639.hp1 HG01496.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2532_209-2531i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579029 | ||||||
chr4:83579030 | CTT | C | 8 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0242 others(5): Show |
8 | HG01106.hp1 HG01109.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.209-2530_209-2529d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579030 | ||||||
chr4:83579031 | T | C | 21 | a0001c0001t0001g0307 a0001c0001t0002g0082 a0001c0001t0002g0214 others(18): Show |
21 | HG01257.hp1 HG01346.hp2 HG02004.hp2 others(18): Show |
intron_variant | MODIFIER | c.209-2531T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579031 | |||||||
chr4:83579033 | T | C | 9 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0242 others(6): Show |
9 | HG01106.hp1 HG01109.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2529T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579033 | |||||||
chr4:83579033 | T | TCC | 4 | a0001c0001t0001g0080 a0001c0001t0001g0148 a0001c0001t0003g0326 others(1): Show |
4 | HG04228.hp1 HG06807.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2528_209-2527i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579033 | ||||||
chr4:83579034 | CTT | C | 6 | a0001c0001t0002g0304 a0001c0001t0002g0319 a0001c0001t0003g0078 others(3): Show |
6 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-2526_209-2525d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579034 | ||||||
chr4:83579035 | T | C | 29 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0307 others(26): Show |
29 | HG01346.hp2 HG01884.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.209-2527T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579035 | |||||||
chr4:83579037 | T | C | 7 | a0001c0001t0002g0304 a0001c0001t0002g0313 a0001c0001t0002g0319 others(4): Show |
7 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-2525T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579037 | |||||||
chr4:83579038 | CTT | C | 4 | a0001c0001t0002g0082 a0001c0001t0002g0252 a0001c0001t0003g0197 others(1): Show |
4 | HG01257.hp1 HG02615.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-2522_209-2521d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579038 | ||||||
chr4:83579039 | T | C | 28 | a0001c0001t0002g0010 a0001c0001t0002g0029 a0001c0001t0002g0208 others(25): Show |
28 | HG01346.hp2 HG01884.hp1 HG02004.hp2 others(25): Show |
intron_variant | MODIFIER | c.209-2523T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579039 | |||||||
chr4:83579041 | T | C | 6 | a0001c0001t0002g0082 a0001c0001t0002g0252 a0001c0001t0002g0313 others(3): Show |
6 | HG01257.hp1 HG02615.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2521T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579041 | |||||||
chr4:83579042 | CTT | C | 11 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(8): Show |
11 | HG00099.hp2 HG02717.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-2518_209-2517d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579042 | ||||||
chr4:83579043 | T | C | 20 | a0001c0001t0002g0208 a0001c0001t0002g0247 a0001c0001t0002g0256 others(17): Show |
20 | HG01192.hp1 HG02004.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.209-2519T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579043 | |||||||
chr4:83579043 | TTTCTTTC others(33): Show |
T | 1 | a0001c0001t0015g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.209-2515_209-2476d others(42): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579043 | ||||||
chr4:83579045 | T | C | 61 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(58): Show |
61 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.209-2517T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579045 | |||||||
chr4:83579045 | T | TCCTTCCT others(194): Show |
1 | a0001c0001t0005g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209-2516_209-2515i others(203): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579045 | ||||||
chr4:83579045 | TCTTTCTT others(29): Show |
T | 1 | a0001c0001t0005g0209 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.209-2515_209-2480d others(38): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579045 | ||||||
chr4:83579046 | CTT | C | 18 | a0001c0001t0002g0010 a0001c0001t0002g0029 a0001c0001t0002g0213 others(15): Show |
18 | HG01346.hp2 HG01884.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-2514_209-2513d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579046 | ||||||
chr4:83579047 | T | C | 16 | a0001c0001t0002g0208 a0001c0001t0002g0247 a0001c0001t0002g0256 others(13): Show |
16 | HG02004.hp2 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-2515T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579047 | |||||||
chr4:83579047 | TTTCTTTC others(33): Show |
T | 11 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0020 others(8): Show |
11 | HG02258.hp2 HG02572.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2511_209-2472d others(42): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579047 | ||||||
chr4:83579049 | T | C | 19 | a0001c0001t0002g0010 a0001c0001t0002g0029 a0001c0001t0002g0213 others(16): Show |
19 | HG01346.hp2 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.209-2513T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579049 | |||||||
chr4:83579049 | T | TCCTTCCT others(194): Show |
1 | a0001c0001t0003g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.209-2512_209-2511i others(203): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579049 | ||||||
chr4:83579049 | TCTTTCTT others(25): Show |
T | 25 | a0001c0001t0002g0007 a0001c0001t0002g0021 a0001c0001t0002g0024 others(22): Show |
25 | HG00408.hp1 HG00438.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.209-2511_209-2480d others(34): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579049 | ||||||
chr4:83579050 | CTT | C | 11 | a0001c0001t0002g0249 a0001c0001t0002g0268 a0001c0001t0002g0270 others(8): Show |
11 | HG01192.hp1 HG02109.hp1 NA18959.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2510_209-2509d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579050 | ||||||
chr4:83579051 | T | C | 15 | a0001c0001t0002g0049 a0001c0001t0002g0215 a0001c0001t0002g0250 others(12): Show |
15 | HG01070.hp2 HG01256.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.209-2511T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579051 | |||||||
chr4:83579053 | T | C | 11 | a0001c0001t0002g0249 a0001c0001t0002g0268 a0001c0001t0002g0270 others(8): Show |
11 | HG01192.hp1 HG02109.hp1 NA18959.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2509T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579053 | |||||||
chr4:83579053 | T | TCC | 11 | a0001c0001t0002g0208 a0001c0001t0002g0247 a0001c0001t0002g0256 others(8): Show |
11 | HG02004.hp2 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2508_209-2507i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579053 | ||||||
chr4:83579053 | T | TCTTTCTT others(190): Show |
1 | a0001c0001t0003g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.209-2500_209-2499i others(199): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579053 | ||||||
chr4:83579053 | TCTTTCTT others(21): Show |
T | 9 | a0001c0001t0002g0049 a0001c0001t0002g0215 a0001c0001t0002g0250 others(6): Show |
9 | HG01256.hp2 HG01433.hp2 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2507_209-2480d others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579053 | ||||||
chr4:83579055 | T | C | 6 | a0001c0001t0002g0253 a0001c0001t0002g0271 a0001c0001t0002g0273 others(3): Show |
6 | HG01070.hp2 HG01517.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2507T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579055 | |||||||
chr4:83579057 | T | C | 2 | a0001c0001t0002g0292 a0001c0001t0006g0212 |
2 | HG00140.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.209-2505T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579057 | |||||||
chr4:83579057 | TCTTTCTT others(17): Show |
T | 3 | a0001c0001t0002g0253 a0001c0001t0002g0273 a0001c0001t0004g0013 |
3 | HG01517.hp1 HG01981.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.209-2503_209-2480d others(26): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579057 | ||||||
chr4:83579059 | T | C | 4 | a0001c0001t0002g0271 a0001c0001t0002g0278 a0001c0001t0006g0212 others(1): Show |
4 | HG01070.hp2 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2503T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579059 | |||||||
chr4:83579059 | TTTCTTTC others(21): Show |
T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0161 |
2 | NA18969.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.209-2499_209-2472d others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579059 | ||||||
chr4:83579061 | T | C | 5 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0002g0223 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-2501T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579061 | |||||||
chr4:83579061 | TCTTTCTT others(13): Show |
T | 2 | a0001c0001t0002g0271 a0001c0001t0002g0278 |
2 | HG01070.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.209-2499_209-2480d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579061 | ||||||
chr4:83579063 | T | C | 4 | a0001c0001t0002g0292 a0001c0001t0006g0212 a0001c0001t0007g0188 others(1): Show |
4 | HG00140.hp1 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2499T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579063 | |||||||
chr4:83579063 | TTTCTTTC others(17): Show |
T | 7 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0003g0030 others(4): Show |
7 | HG01109.hp1 HG02486.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-2495_209-2472d others(26): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579063 | ||||||
chr4:83579063 | TTTCTTTC others(21): Show |
T | 1 | a0001c0001t0003g0237 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.209-2495_209-2468d others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579063 | ||||||
chr4:83579063 | TTTCTTTC others(25): Show |
T | 2 | a0001c0001t0002g0242 a0001c0001t0003g0060 |
2 | NA18944.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.209-2495_209-2464d others(34): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579063 | ||||||
chr4:83579065 | T | C | 8 | a0001c0001t0002g0313 a0001c0001t0003g0296 a0001c0001t0003g0303 others(5): Show |
8 | HG01169.hp2 HG01891.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2497T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579065 | |||||||
chr4:83579065 | TCTTTCTT others(9): Show |
T | 1 | a0001c0001t0002g0292 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.209-2495_209-2480d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579065 | ||||||
chr4:83579066 | C | T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2496C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579066 | |||||||
chr4:83579067 | T | C | 5 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0006g0212 others(2): Show |
5 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2495T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579067 | |||||||
chr4:83579067 | T | TTCCCTTC others(5): Show |
1 | a0001c0001t0001g0142 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.209-2494_209-2493i others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579067 | ||||||
chr4:83579067 | TTTCTTTC others(9): Show |
T | 2 | a0001c0001t0003g0046 a0001c0001t0003g0175 |
2 | HG03831.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.209-2491_209-2476d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579067 | ||||||
chr4:83579067 | TTTCTTTC others(13): Show |
T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0064 others(6): Show |
9 | HG00609.hp1 HG03490.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.209-2491_209-2472d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579067 | ||||||
chr4:83579067 | TTTCTTTC others(17): Show |
T | 2 | a0001c0001t0003g0054 a0001c0001t0003g0288 |
2 | HG02257.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.209-2491_209-2468d others(26): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579067 | ||||||
chr4:83579069 | T | C | 8 | a0001c0001t0002g0082 a0001c0001t0002g0252 a0001c0001t0002g0313 others(5): Show |
8 | HG00099.hp1 HG01257.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2493T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579069 | |||||||
chr4:83579069 | T | TC | 3 | a0001c0001t0004g0221 a0002c0002t0003g0145 a0002c0002t0003g0146 |
3 | HG01257.hp2 HG01258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.209-2492dupC | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579069 | ||||||
chr4:83579069 | T | TCCTTCCT others(6): Show |
1 | a0001c0001t0005g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.209-2492_209-2491i others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579069 | ||||||
chr4:83579069 | T | TCCTTCCT others(10): Show |
1 | a0001c0001t0006g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.209-2492_209-2491i others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579069 | ||||||
chr4:83579071 | T | C | 13 | a0001c0001t0001g0090 a0001c0001t0001g0142 a0001c0001t0002g0219 others(10): Show |
13 | HG00099.hp1 HG01081.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-2491T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579071 | |||||||
chr4:83579071 | TTTCTTTC others(5): Show |
T | 2 | a0001c0001t0003g0039 a0001c0001t0003g0218 |
2 | HG00280.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.209-2487_209-2476d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579071 | ||||||
chr4:83579071 | TTTCTTTC others(9): Show |
T | 3 | a0001c0001t0001g0052 a0001c0001t0003g0001 a0001c0001t0003g0191 |
4 | HG00280.hp1 HG03834.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2487_209-2472d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579071 | ||||||
chr4:83579071 | TTTCTTTC others(13): Show |
T | 2 | a0001c0001t0003g0153 a0001c0001t0003g0301 |
2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.209-2487_209-2468d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579071 | ||||||
chr4:83579073 | T | C | 18 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 others(15): Show |
18 | HG00099.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-2489T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579073 | |||||||
chr4:83579073 | T | TCCTTCCT others(10): Show |
1 | a0001c0001t0006g0002 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.209-2488_209-2487i others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579073 | ||||||
chr4:83579075 | T | C | 18 | a0001c0001t0001g0076 a0001c0001t0001g0127 a0001c0001t0001g0142 others(15): Show |
18 | HG00099.hp1 HG01081.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-2487T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579075 | |||||||
chr4:83579075 | T | TTTCTTTC others(7): Show |
1 | a0001c0001t0001g0164 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.209-2482_209-2481i others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579075 | ||||||
chr4:83579075 | TTTCTTCC others(5): Show |
T | 3 | a0001c0001t0003g0025 a0001c0001t0003g0056 a0001c0001t0003g0069 |
3 | NA19057.hp2 NA19064.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.209-2483_209-2472d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579075 | ||||||
chr4:83579075 | TTTCTTCC others(9): Show |
T | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.209-2483_209-2468d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579075 | ||||||
chr4:83579077 | T | C | 22 | a0001c0001t0002g0029 a0001c0001t0002g0222 a0001c0001t0002g0264 others(19): Show |
22 | HG00642.hp2 HG00733.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.209-2485T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579077 | |||||||
chr4:83579079 | T | C | 28 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0238 others(25): Show |
28 | HG00099.hp1 HG00099.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.209-2483T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579079 | |||||||
chr4:83579079 | TTCCCTTC others(1): Show |
T | 17 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0018 others(14): Show |
17 | HG00140.hp2 HG00597.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.209-2481_209-2474d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579079 | ||||||
chr4:83579079 | TTCCCTTC others(5): Show |
T | 1 | a0001c0001t0003g0293 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.209-2481_209-2470d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579079 | ||||||
chr4:83579081 | C | CCCTT | 25 | a0001c0001t0001g0008 a0001c0001t0001g0070 a0001c0001t0001g0077 others(22): Show |
25 | HG00438.hp1 HG01106.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.209-2436_209-2433d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | C | CCCTTCCT others(1): Show |
10 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0099 others(7): Show |
10 | HG01993.hp1 HG02015.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.209-2440_209-2433d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | C | CCCTTCCT others(5): Show |
6 | a0001c0001t0001g0123 a0001c0001t0001g0150 a0001c0001t0001g0158 others(3): Show |
6 | HG02071.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-2444_209-2433d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | C | CCCTTCCT others(9): Show |
4 | a0001c0001t0001g0148 a0001c0001t0004g0019 a0001c0001t0005g0331 others(1): Show |
4 | HG02965.hp2 HG03579.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2448_209-2433d others(18): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | C | CCCTTCCT others(13): Show |
1 | a0001c0001t0002g0332 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.209-2452_209-2433d others(22): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | C | CCCTTCCT others(17): Show |
1 | a0001c0001t0001g0144 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209-2456_209-2433d others(26): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | C | CCCTTCCT others(21): Show |
1 | a0001c0001t0001g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.209-2460_209-2433d others(30): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | C | CCTT | 7 | a0001c0001t0004g0221 a0001c0001t0005g0198 a0001c0001t0006g0002 others(4): Show |
7 | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-2480_209-2479i others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | C | CCTTCCTT others(16): Show |
1 | a0001c0001t0006g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.209-2480_209-2479i others(25): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | C | T | 54 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0165 others(51): Show |
54 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.209-2481C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579081 | |||||||
chr4:83579081 | CCCTT | C | 24 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0001g0097 others(21): Show |
24 | HG00597.hp2 HG00609.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.209-2436_209-2433d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | CCCTTCCT others(1): Show |
C | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0035 others(5): Show |
8 | HG00741.hp2 HG01515.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2440_209-2433d others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579081 | CCCTTCCT others(5): Show |
C | 1 | a0001c0001t0004g0200 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.209-2444_209-2433d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579081 | ||||||
chr4:83579083 | C | T | 36 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(33): Show |
36 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.209-2479C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579083 | |||||||
chr4:83579085 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0015g0180 |
2 | HG02055.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.209-2477T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579085 | |||||||
chr4:83579087 | C | T | 13 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0003g0005 others(10): Show |
13 | HG00639.hp1 HG00733.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-2475C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579087 | |||||||
chr4:83579130 | T | C | 76 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(73): Show |
77 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.209-2432T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579130 | |||||||
chr4:83579132 | T | C | 1 | a0001c0001t0002g0280 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.209-2430T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579132 | |||||||
chr4:83579134 | T | C | 3 | a0001c0001t0002g0258 a0001c0001t0004g0115 a0001c0001t0004g0309 |
3 | HG01261.hp2 HG02109.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.209-2428T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579134 | |||||||
chr4:83579137 | C | T | 1 | a0001c0001t0004g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2425C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579137 | |||||||
chr4:83579141 | C | T | 1 | a0001c0001t0004g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2421C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579141 | |||||||
chr4:83579146 | CCT | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-2407_209-2406d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579146 | ||||||
chr4:83579150 | T | C | 1 | a0001c0001t0004g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2412T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579150 | |||||||
chr4:83579154 | T | C | 1 | a0001c0001t0004g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2408T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579154 | |||||||
chr4:83579157 | T | C | 1 | a0001c0001t0004g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-2405T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579157 | |||||||
chr4:83579278 | T | TTCCCC | 5 | a0001c0001t0002g0098 a0001c0001t0002g0291 a0001c0001t0005g0182 others(2): Show |
5 | HG00099.hp1 HG01106.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2260_209-2256d others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579278 | ||||||
chr4:83579278 | TTCCCC | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01081.hp1 HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.209-2260_209-2256d others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83579278 | ||||||
chr4:83579368 | C | T | 11 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2194C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579368 | |||||||
chr4:83579403 | C | G | 4 | a0001c0001t0003g0030 a0001c0001t0003g0058 a0001c0001t0003g0059 others(1): Show |
4 | NA18946.hp1 NA18964.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2159C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579403 | |||||||
chr4:83579404 | T | C | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2158T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579404 | |||||||
chr4:83579405 | G | T | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2157G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579405 | |||||||
chr4:83579406 | C | G | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-2156C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579406 | |||||||
chr4:83579482 | A | G | 11 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-2080A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579482 | |||||||
chr4:83579848 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.209-1714A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579848 | |||||||
chr4:83579857 | C | T | 1 | a0001c0001t0004g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.209-1705C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83579857 | |||||||
chr4:83580140 | A | G | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-1422A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580140 | |||||||
chr4:83580310 | C | A | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.209-1252C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580310 | |||||||
chr4:83580362 | CTTGA | C | 5 | a0001c0001t0002g0082 a0001c0001t0002g0259 a0001c0001t0002g0260 others(2): Show |
5 | NA18943.hp2 NA18948.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-1197_209-1194d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83580362 | ||||||
chr4:83580572 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.209-990C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580572 | |||||||
chr4:83580810 | A | G | 109 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(106): Show |
109 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.209-752A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580810 | |||||||
chr4:83580814 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.209-748C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580814 | |||||||
chr4:83580892 | T | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-670T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580892 | |||||||
chr4:83580965 | G | A | 1 | a0001c0004t0004g0305 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.209-597G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580965 | |||||||
chr4:83580968 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.209-594T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83580968 | |||||||
chr4:83581025 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.209-537G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83581025 | |||||||
chr4:83581065 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.209-497C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83581065 | |||||||
chr4:83581095 | C | CA | 119 | a0001c0001t0001g0034 a0001c0001t0001g0070 a0001c0001t0001g0086 others(116): Show |
119 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.209-441dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83581095 | ||||||
chr4:83581095 | C | CAA | 46 | a0001c0001t0001g0158 a0001c0001t0001g0216 a0001c0001t0001g0307 others(43): Show |
46 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.209-442_209-441dup others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83581095 | ||||||
chr4:83581095 | CAAAAAAA | C | 10 | a0001c0001t0003g0030 a0001c0001t0003g0045 a0001c0001t0003g0046 others(7): Show |
10 | HG01070.hp1 HG02602.hp2 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-447_209-441del others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83581095 | ||||||
chr4:83581095 | CAAAAAAA others(1): Show |
C | 62 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(59): Show |
63 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.209-448_209-441del others(8): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr4 | 83581095 | ||||||
chr4:83581218 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.209-344C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83581218 | |||||||
chr4:83581449 | A | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.209-113A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83581449 | |||||||
chr4:83581523 | C | T | 4 | a0001c0001t0001g0254 a0001c0001t0005g0198 a0001c0001t0006g0002 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-39C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 2/11 | chr4 | 83581523 | |||||||
chr4:83581891 | T | C | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.479+59T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83581891 | |||||||
chr4:83581972 | A | G | 232 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.479+140A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83581972 | |||||||
chr4:83581973 | A | C | 232 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.479+141A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83581973 | |||||||
chr4:83582138 | GGAA | G | 13 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0003g0197 others(10): Show |
13 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.479+318_479+320del others(3): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83582138 | ||||||
chr4:83582205 | T | C | 1 | a0001c0001t0003g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.479+373T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582205 | |||||||
chr4:83582222 | C | T | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.479+390C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582222 | |||||||
chr4:83582289 | C | T | 1 | a0001c0001t0002g0291 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.479+457C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582289 | |||||||
chr4:83582344 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.479+512G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582344 | |||||||
chr4:83582352 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.479+520C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582352 | |||||||
chr4:83582411 | G | A | 1 | a0001c0001t0003g0061 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.479+579G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582411 | |||||||
chr4:83582446 | C | T | 7 | a0001c0001t0001g0112 a0001c0001t0004g0199 a0001c0001t0004g0200 others(4): Show |
7 | HG01243.hp2 HG02055.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.479+614C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582446 | |||||||
chr4:83582447 | G | A | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+615G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582447 | |||||||
chr4:83582474 | C | T | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+642C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582474 | |||||||
chr4:83582689 | C | G | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+857C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582689 | |||||||
chr4:83582756 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.479+924C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582756 | |||||||
chr4:83582786 | G | GT | 71 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(68): Show |
72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.479+963dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83582786 | ||||||
chr4:83582786 | G | T | 1 | a0001c0001t0003g0288 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.479+954G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582786 | |||||||
chr4:83582861 | A | G | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.479+1029A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83582861 | |||||||
chr4:83583072 | C | T | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+1240C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583072 | |||||||
chr4:83583186 | C | T | 6 | a0001c0001t0005g0182 a0001c0001t0005g0205 a0001c0001t0005g0225 others(3): Show |
6 | HG00099.hp1 HG03130.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.479+1354C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583186 | |||||||
chr4:83583293 | C | CA | 9 | a0001c0001t0002g0299 a0001c0001t0002g0310 a0001c0001t0002g0322 others(6): Show |
9 | HG00099.hp1 HG03130.hp1 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.479+1471dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583293 | ||||||
chr4:83583295 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.479+1463A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583295 | |||||||
chr4:83583333 | C | T | 1 | a0001c0001t0002g0263 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.479+1501C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583333 | |||||||
chr4:83583482 | A | G | 13 | a0001c0001t0005g0012 a0001c0001t0005g0014 a0001c0001t0005g0196 others(10): Show |
13 | HG02055.hp1 HG02809.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.479+1650A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583482 | |||||||
chr4:83583517 | A | G | 4 | a0001c0001t0006g0212 a0001c0001t0007g0188 a0001c0001t0007g0189 others(1): Show |
4 | HG02615.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+1685A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583517 | |||||||
chr4:83583624 | G | A | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.479+1792G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583624 | |||||||
chr4:83583638 | G | A | 3 | a0001c0001t0004g0013 a0001c0001t0004g0306 a0001c0001t0005g0245 |
3 | HG01243.hp1 HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.479+1806G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583638 | |||||||
chr4:83583644 | G | T | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+1812G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583644 | |||||||
chr4:83583656 | G | A | 11 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+1824G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583656 | |||||||
chr4:83583658 | C | G | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.479+1826C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583658 | |||||||
chr4:83583666 | T | TGAA | 16 | a0001c0001t0001g0050 a0001c0001t0003g0015 a0001c0001t0003g0030 others(13): Show |
16 | HG00597.hp1 HG00609.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.479+1835_479+1837d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583666 | ||||||
chr4:83583667 | G | GA | 121 | a0001c0001t0001g0008 a0001c0001t0001g0070 a0001c0001t0001g0083 others(118): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.479+1865dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | ||||||
chr4:83583667 | G | GAA | 35 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(32): Show |
35 | HG00642.hp2 HG01109.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.479+1864_479+1865d others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | ||||||
chr4:83583667 | G | GAAAAAAA others(3): Show |
2 | a0001c0001t0007g0189 a0001c0001t0007g0190 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.479+1856_479+1865d others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | ||||||
chr4:83583667 | G | GAAAAAAA others(4): Show |
4 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0006g0002 others(1): Show |
4 | HG01891.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.479+1855_479+1865d others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | ||||||
chr4:83583667 | G | GAAAAAAA others(5): Show |
1 | a0001c0001t0004g0221 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.479+1854_479+1865d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | ||||||
chr4:83583667 | G | GAAAAAAA others(6): Show |
1 | a0001c0001t0006g0003 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.479+1853_479+1865d others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583667 | ||||||
chr4:83583668 | A | AAG | 53 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0065 others(50): Show |
54 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.479+1837_479+1838i others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83583668 | ||||||
chr4:83583704 | T | G | 1 | a0001c0001t0002g0313 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.479+1872T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583704 | |||||||
chr4:83583826 | T | G | 11 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.479+1994T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583826 | |||||||
chr4:83583955 | G | A | 2 | a0001c0001t0004g0031 a0001c0001t0004g0033 |
2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.479+2123G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83583955 | |||||||
chr4:83584170 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.479+2338C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584170 | |||||||
chr4:83584378 | C | T | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+2546C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584378 | |||||||
chr4:83584457 | G | A | 4 | a0001c0001t0002g0299 a0001c0001t0002g0310 a0001c0001t0002g0313 others(1): Show |
4 | NA18947.hp2 NA18975.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.479+2625G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584457 | |||||||
chr4:83584488 | A | C | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+2656A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584488 | |||||||
chr4:83584497 | A | C | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.479+2665A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584497 | |||||||
chr4:83584564 | G | C | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-2691G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584564 | |||||||
chr4:83584564 | G | T | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.480-2691G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584564 | |||||||
chr4:83584565 | A | G | 86 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(83): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.480-2690A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584565 | |||||||
chr4:83584609 | G | T | 1 | a0001c0001t0002g0136 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.480-2646G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584609 | |||||||
chr4:83584698 | G | T | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-2557G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584698 | |||||||
chr4:83584718 | C | T | 1 | a0001c0001t0003g0237 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.480-2537C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584718 | |||||||
chr4:83584863 | T | C | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-2392T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584863 | |||||||
chr4:83584920 | C | G | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-2335C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83584920 | |||||||
chr4:83585039 | T | C | 124 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0238 others(121): Show |
124 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.480-2216T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585039 | |||||||
chr4:83585095 | G | A | 6 | a0001c0001t0003g0001 a0001c0001t0003g0047 a0001c0001t0003g0048 others(3): Show |
7 | HG01109.hp2 HG01175.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.480-2160G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585095 | |||||||
chr4:83585127 | A | C | 72 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.480-2128A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585127 | |||||||
chr4:83585197 | A | G | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-2058A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585197 | |||||||
chr4:83585210 | A | G | 1 | a0001c0001t0005g0012 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.480-2045A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585210 | |||||||
chr4:83585294 | T | C | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1961T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585294 | |||||||
chr4:83585331 | A | C | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1924A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585331 | |||||||
chr4:83585340 | G | A | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1915G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585340 | |||||||
chr4:83585383 | A | G | 1 | a0001c0001t0002g0273 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.480-1872A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585383 | |||||||
chr4:83585513 | A | C | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1742A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585513 | |||||||
chr4:83585594 | T | C | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1661T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585594 | |||||||
chr4:83585615 | CT | C | 74 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(71): Show |
75 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.480-1627delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83585615 | ||||||
chr4:83585716 | G | A | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.480-1539G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585716 | |||||||
chr4:83585833 | C | T | 3 | a0001c0001t0005g0182 a0001c0001t0005g0205 a0001c0001t0005g0225 |
3 | HG00099.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.480-1422C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585833 | |||||||
chr4:83585851 | T | G | 1 | a0001c0001t0013g0171 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.480-1404T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585851 | |||||||
chr4:83585852 | G | A | 1 | a0001c0001t0004g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.480-1403G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585852 | |||||||
chr4:83585876 | T | C | 1 | a0001c0001t0004g0309 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.480-1379T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83585876 | |||||||
chr4:83585975 | G | GCCAGACT | 14 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0003g0194 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.480-1278_480-1277i others(9): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr4 | 83585975 | ||||||
chr4:83586119 | A | C | 85 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(82): Show |
86 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.480-1136A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586119 | |||||||
chr4:83586137 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.480-1118G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586137 | |||||||
chr4:83586154 | G | A | 1 | a0001c0001t0012g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.480-1101G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586154 | |||||||
chr4:83586183 | C | G | 11 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0004g0221 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.480-1072C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586183 | |||||||
chr4:83586399 | A | G | 14 | a0001c0001t0002g0219 a0001c0001t0002g0220 a0001c0001t0003g0194 others(11): Show |
14 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.480-856A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586399 | |||||||
chr4:83586409 | T | C | 1 | a0001c0001t0005g0182 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.480-846T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586409 | |||||||
chr4:83586589 | A | T | 218 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.480-666A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586589 | |||||||
chr4:83586890 | C | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0078 |
2 | HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.480-365C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83586890 | |||||||
chr4:83587018 | G | A | 6 | a0001c0001t0005g0182 a0001c0001t0005g0184 a0001c0001t0005g0205 others(3): Show |
6 | HG00099.hp1 HG03130.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.480-237G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 3/11 | chr4 | 83587018 | |||||||
chr4:83587543 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.554+214C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 4/11 | chr4 | 83587543 | |||||||
chr4:83587611 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.554+282A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 4/11 | chr4 | 83587611 | |||||||
chr4:83587676 | T | G | 21 | a0001c0001t0003g0197 a0001c0001t0004g0221 a0001c0001t0005g0004 others(18): Show |
21 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.554+347T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 4/11 | chr4 | 83587676 | |||||||
chr4:83588032 | A | G | 2 | a0001c0001t0005g0318 a0001c0001t0014g0181 |
2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.555-178A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 4/11 | chr4 | 83588032 | |||||||
chr4:83588073 | A | T | 8 | a0001c0001t0004g0221 a0001c0001t0006g0002 a0001c0001t0006g0003 others(5): Show |
8 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-137A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 4/11 | chr4 | 83588073 | |||||||
chr4:83588444 | G | A | 9 | a0001c0001t0002g0082 a0001c0001t0002g0259 a0001c0001t0002g0260 others(6): Show |
9 | NA18943.hp2 NA18948.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.644+145G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588444 | |||||||
chr4:83588502 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0300 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.644+203C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588502 | |||||||
chr4:83588584 | A | C | 8 | a0001c0001t0003g0183 a0001c0001t0003g0194 a0001c0001t0005g0182 others(5): Show |
8 | HG00099.hp1 HG02258.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.644+285A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588584 | |||||||
chr4:83588698 | C | G | 8 | a0001c0001t0002g0208 a0001c0001t0002g0213 a0001c0001t0002g0214 others(5): Show |
8 | HG01884.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.644+399C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588698 | |||||||
chr4:83588744 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.644+445T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588744 | |||||||
chr4:83588855 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.644+556C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83588855 | |||||||
chr4:83589085 | G | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01081.hp1 HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.644+786G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83589085 | |||||||
chr4:83589297 | A | G | 2 | a0001c0001t0005g0198 a0001c0001t0005g0245 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.645-902A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83589297 | |||||||
chr4:83590055 | T | C | 1 | a0001c0001t0003g0293 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.645-144T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 5/11 | chr4 | 83590055 | |||||||
chr4:83590401 | C | T | 6 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
6 | NA18946.hp2 NA18947.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.738+109C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83590401 | |||||||
chr4:83590429 | T | C | 11 | a0001c0001t0003g0183 a0001c0001t0003g0194 a0001c0001t0005g0182 others(8): Show |
11 | HG00099.hp1 HG02258.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.738+137T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83590429 | |||||||
chr4:83590457 | G | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0047 a0001c0001t0003g0048 others(4): Show |
8 | HG01109.hp2 HG01175.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.738+165G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83590457 | |||||||
chr4:83590571 | T | C | 173 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(170): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.738+279T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83590571 | |||||||
chr4:83590856 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.738+564T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83590856 | |||||||
chr4:83590885 | C | CT | 76 | a0001c0001t0001g0089 a0001c0001t0001g0118 a0001c0001t0002g0007 others(73): Show |
77 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.738+613dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83590885 | ||||||
chr4:83590885 | CT | C | 28 | a0001c0001t0001g0105 a0001c0001t0001g0132 a0001c0001t0001g0162 others(25): Show |
28 | HG00099.hp1 HG00099.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.738+613delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83590885 | ||||||
chr4:83591060 | G | A | 3 | a0001c0001t0003g0183 a0001c0001t0003g0194 a0001c0001t0005g0331 |
3 | HG02258.hp1 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.738+768G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591060 | |||||||
chr4:83591142 | G | A | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.738+850G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591142 | |||||||
chr4:83591236 | G | A | 173 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(170): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.738+944G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591236 | |||||||
chr4:83591275 | A | G | 1 | a0001c0004t0004g0305 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.738+983A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591275 | |||||||
chr4:83591299 | A | T | 2 | a0001c0001t0005g0198 a0001c0001t0005g0245 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.738+1007A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591299 | |||||||
chr4:83591300 | G | T | 2 | a0001c0001t0005g0198 a0001c0001t0005g0245 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.738+1008G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591300 | |||||||
chr4:83591301 | G | T | 2 | a0001c0001t0005g0198 a0001c0001t0005g0245 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.738+1009G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591301 | |||||||
chr4:83591302 | C | T | 2 | a0001c0001t0005g0198 a0001c0001t0005g0245 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.738+1010C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591302 | |||||||
chr4:83591330 | T | C | 1 | a0001c0001t0003g0303 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.738+1038T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591330 | |||||||
chr4:83591740 | G | C | 1 | a0001c0001t0003g0001 | 2 | HG03834.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.738+1448G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591740 | |||||||
chr4:83591802 | T | C | 1 | a0001c0001t0004g0147 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.738+1510T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83591802 | |||||||
chr4:83592153 | C | A | 1 | a0001c0001t0005g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.738+1861C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592153 | |||||||
chr4:83592230 | A | G | 8 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0148 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.738+1938A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592230 | |||||||
chr4:83592236 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.738+1944G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592236 | |||||||
chr4:83592285 | C | G | 1 | a0001c0001t0005g0245 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.738+1993C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592285 | |||||||
chr4:83592394 | T | C | 2 | a0001c0001t0004g0019 a0001c0001t0004g0227 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.738+2102T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592394 | |||||||
chr4:83592497 | A | G | 72 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.738+2205A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592497 | |||||||
chr4:83592825 | A | G | 1 | a0001c0001t0003g0056 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.739-2020A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592825 | |||||||
chr4:83592952 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.739-1893C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83592952 | |||||||
chr4:83593045 | T | G | 1 | a0001c0001t0002g0230 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.739-1800T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593045 | |||||||
chr4:83593166 | C | CTTTTTTT others(5): Show |
39 | a0001c0001t0003g0001 a0001c0001t0003g0006 a0001c0001t0003g0016 others(36): Show |
40 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.739-1673_739-1662d others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83593166 | ||||||
chr4:83593166 | C | CTTTTTTT others(6): Show |
29 | a0001c0001t0003g0005 a0001c0001t0003g0015 a0001c0001t0003g0025 others(26): Show |
29 | HG00597.hp1 HG00733.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.739-1674_739-1662d others(15): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83593166 | ||||||
chr4:83593166 | C | CTTTTTTT others(7): Show |
6 | a0001c0001t0003g0042 a0001c0001t0003g0053 a0001c0001t0003g0057 others(3): Show |
6 | HG02056.hp1 HG02738.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.739-1675_739-1662d others(16): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83593166 | ||||||
chr4:83593307 | G | A | 1 | a0001c0001t0003g0030 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.739-1538G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593307 | |||||||
chr4:83593380 | G | T | 1 | a0001c0001t0004g0115 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.739-1465G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593380 | |||||||
chr4:83593429 | G | A | 4 | a0001c0001t0006g0212 a0001c0001t0007g0188 a0001c0001t0007g0189 others(1): Show |
4 | HG02615.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-1416G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593429 | |||||||
chr4:83593449 | AACC | A | 11 | a0001c0001t0005g0012 a0001c0001t0005g0014 a0001c0001t0005g0196 others(8): Show |
11 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.739-1390_739-1388d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr4 | 83593449 | ||||||
chr4:83593740 | T | C | 1 | a0001c0001t0003g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.739-1105T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593740 | |||||||
chr4:83593821 | A | G | 3 | a0001c0001t0005g0182 a0001c0001t0005g0205 a0001c0001t0005g0225 |
3 | HG00099.hp1 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.739-1024A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593821 | |||||||
chr4:83593931 | G | A | 2 | a0001c0001t0009g0186 a0001c0001t0009g0187 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.739-914G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593931 | |||||||
chr4:83593977 | A | G | 1 | a0001c0001t0003g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.739-868A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83593977 | |||||||
chr4:83594246 | T | C | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.739-599T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594246 | |||||||
chr4:83594254 | C | T | 3 | a0001c0001t0005g0184 a0001c0001t0005g0198 a0001c0001t0005g0245 |
3 | HG02818.hp1 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.739-591C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594254 | |||||||
chr4:83594428 | T | G | 2 | a0001c0001t0005g0198 a0001c0001t0005g0245 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.739-417T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594428 | |||||||
chr4:83594503 | T | C | 5 | a0001c0001t0002g0007 a0001c0001t0002g0020 a0001c0001t0002g0021 others(2): Show |
5 | HG02486.hp2 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.739-342T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594503 | |||||||
chr4:83594622 | G | A | 102 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(99): Show |
102 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.739-223G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594622 | |||||||
chr4:83594640 | C | T | 2 | a0001c0001t0003g0183 a0001c0001t0005g0331 |
2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.739-205C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594640 | |||||||
chr4:83594815 | C | T | 72 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.739-30C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 6/11 | chr4 | 83594815 | |||||||
chr4:83595012 | A | G | 11 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0142 others(8): Show |
11 | HG01081.hp1 HG01884.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.854+52A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595012 | |||||||
chr4:83595038 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0172 |
2 | NA18947.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.854+78C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595038 | |||||||
chr4:83595323 | A | AT | 11 | a0001c0001t0005g0012 a0001c0001t0005g0014 a0001c0001t0005g0196 others(8): Show |
11 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.854+363_854+364ins others(1): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595323 | |||||||
chr4:83595346 | C | A | 6 | a0001c0001t0001g0117 a0001c0001t0001g0125 a0001c0001t0001g0162 others(3): Show |
6 | HG02027.hp1 HG02040.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.854+386C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595346 | |||||||
chr4:83595346 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.854+386C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595346 | |||||||
chr4:83595536 | G | A | 177 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(174): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.854+576G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595536 | |||||||
chr4:83595603 | G | A | 2 | a0001c0001t0004g0019 a0001c0001t0004g0227 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.854+643G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595603 | |||||||
chr4:83595607 | C | G | 1 | a0001c0001t0003g0293 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.854+647C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595607 | |||||||
chr4:83595611 | T | C | 7 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0206 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.854+651T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595611 | |||||||
chr4:83595629 | G | A | 9 | a0001c0001t0003g0197 a0001c0001t0005g0004 a0001c0001t0006g0002 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.854+669G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595629 | |||||||
chr4:83595713 | TA | T | 10 | a0001c0001t0001g0105 a0001c0001t0001g0121 a0001c0001t0001g0132 others(7): Show |
10 | HG01169.hp1 HG01169.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.854+765delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr4 | 83595713 | ||||||
chr4:83595762 | A | G | 4 | a0001c0001t0002g0299 a0001c0001t0002g0310 a0001c0001t0002g0313 others(1): Show |
4 | NA18947.hp2 NA18975.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.854+802A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595762 | |||||||
chr4:83595937 | C | T | 3 | a0001c0001t0003g0296 a0001c0001t0003g0303 a0001c0001t0003g0327 |
3 | HG01169.hp2 HG02698.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.855-921C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83595937 | |||||||
chr4:83596233 | C | G | 71 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(68): Show |
72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.855-625C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596233 | |||||||
chr4:83596391 | C | T | 12 | a0001c0001t0005g0004 a0001c0001t0005g0012 a0001c0001t0005g0014 others(9): Show |
12 | HG02723.hp2 HG02809.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.855-467C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596391 | |||||||
chr4:83596437 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.855-421A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596437 | |||||||
chr4:83596628 | A | C | 1 | a0001c0001t0002g0249 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.855-230A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596628 | |||||||
chr4:83596629 | C | A | 1 | a0001c0001t0002g0249 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.855-229C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596629 | |||||||
chr4:83596631 | A | C | 1 | a0001c0001t0002g0249 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.855-227A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596631 | |||||||
chr4:83596851 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19062.hp2 | splice_region_variant&intron_variant | LOW | c.855-7T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596851 | |||||||
chr4:83596854 | A | G | 1 | a0001c0001t0002g0269 | 1 | NA18969.hp1 | splice_region_variant&intron_variant | LOW | c.855-4A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 7/11 | chr4 | 83596854 | |||||||
chr4:83597162 | G | T | 177 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(174): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.910+249G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 8/11 | chr4 | 83597162 | |||||||
chr4:83597184 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.911-246C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 8/11 | chr4 | 83597184 | |||||||
chr4:83597211 | A | G | 5 | a0001c0001t0005g0004 a0001c0001t0006g0002 a0001c0001t0006g0003 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.911-219A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 8/11 | chr4 | 83597211 | |||||||
chr4:83597341 | A | G | 2 | a0001c0001t0004g0019 a0001c0001t0004g0227 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.911-89A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 8/11 | chr4 | 83597341 | |||||||
chr4:83597405 | C | T | 72 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.911-25C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 8/11 | chr4 | 83597405 | |||||||
chr4:83597678 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.996+163C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597678 | |||||||
chr4:83597688 | A | G | 1 | a0001c0001t0006g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.996+173A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597688 | |||||||
chr4:83597739 | A | G | 11 | a0001c0001t0003g0183 a0001c0001t0003g0197 a0001c0001t0005g0182 others(8): Show |
11 | HG00099.hp1 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.996+224A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597739 | |||||||
chr4:83597755 | CAG | C | 5 | a0001c0001t0003g0025 a0001c0001t0003g0037 a0001c0001t0003g0039 others(2): Show |
5 | HG00597.hp1 HG02015.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.996+242_996+243del others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr4 | 83597755 | ||||||
chr4:83597923 | A | G | 188 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.997-128A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597923 | |||||||
chr4:83597997 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.997-54C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597997 | |||||||
chr4:83597998 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.997-53G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 9/11 | chr4 | 83597998 | |||||||
chr4:83598277 | T | C | 1 | a0001c0001t0005g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1125+98T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | chr4 | 83598277 | |||||||
chr4:83598430 | C | T | 1 | a0001c0001t0002g0314 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1126-214C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | chr4 | 83598430 | |||||||
chr4:83598486 | T | G | 214 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1126-158T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | chr4 | 83598486 | |||||||
chr4:83598622 | A | AT | 19 | a0001c0001t0002g0252 a0001c0001t0002g0257 a0001c0001t0002g0268 others(16): Show |
19 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(16): Show |
splice_region_variant&intron_variant | LOW | c.1126-8dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 83598622 | ||||||
chr4:83598622 | AT | A | 71 | a0001c0001t0001g0124 a0001c0001t0001g0179 a0001c0001t0002g0255 others(68): Show |
72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
splice_region_variant&intron_variant | LOW | c.1126-8delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr4 | 83598622 | ||||||
chr4:83598625 | T | G | 16 | a0001c0001t0005g0004 a0001c0001t0005g0012 a0001c0001t0005g0014 others(13): Show |
16 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1126-19T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 10/11 | chr4 | 83598625 | |||||||
chr4:83598751 | C | CT | 11 | a0001c0001t0001g0008 a0001c0001t0001g0080 a0001c0001t0001g0103 others(8): Show |
11 | HG01433.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1205+64dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | C | CTT | 7 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0004g0031 others(4): Show |
7 | HG00099.hp1 HG01496.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.1205+63_1205+64dup others(2): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | C | CTTT | 8 | a0001c0001t0002g0219 a0001c0001t0002g0264 a0001c0001t0002g0276 others(5): Show |
8 | HG02040.hp1 HG02897.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1205+62_1205+64dup others(3): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | C | CTTTT | 50 | a0001c0001t0001g0217 a0001c0001t0002g0020 a0001c0001t0002g0021 others(47): Show |
50 | HG00099.hp2 HG00408.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1205+61_1205+64dup others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | C | CTTTTT | 44 | a0001c0001t0001g0216 a0001c0001t0002g0007 a0001c0001t0002g0009 others(41): Show |
44 | HG00140.hp1 HG00438.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1205+60_1205+64dup others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | C | CTTTTTT | 8 | a0001c0001t0002g0011 a0001c0001t0002g0277 a0001c0001t0002g0299 others(5): Show |
8 | HG00733.hp1 HG02004.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.1205+59_1205+64dup others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | CT | C | 58 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0035 others(55): Show |
58 | HG00438.hp1 HG00597.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.1205+64delT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | CTTTT | C | 17 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0026 others(14): Show |
17 | HG00140.hp2 HG00639.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1205+61_1205+64del others(4): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | CTTTTT | C | 52 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0015 others(49): Show |
52 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1205+60_1205+64del others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | CTTTTTT | C | 6 | a0001c0001t0002g0330 a0001c0001t0003g0001 a0001c0001t0003g0047 others(3): Show |
7 | HG01175.hp1 HG02004.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1205+59_1205+64del others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0227 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1205+55_1205+64del others(10): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0019 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1205+54_1205+64del others(11): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0307 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1205+52_1205+64del others(13): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0079 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1205+51_1205+64del others(14): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0002g0273 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1205+46_1205+64del others(19): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598751 | CTTTTTTT others(17): Show |
C | 7 | a0001c0001t0005g0012 a0001c0001t0005g0196 a0001c0001t0005g0207 others(4): Show |
7 | HG02896.hp1 HG02897.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1205+41_1205+64del others(24): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598751 | ||||||
chr4:83598830 | ATGATCAT others(14): Show |
A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0164 |
2 | HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1205+130_1205+150d others(23): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83598830 | ||||||
chr4:83598877 | C | T | 71 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(68): Show |
72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1205+154C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83598877 | |||||||
chr4:83598888 | C | G | 11 | a0001c0001t0005g0012 a0001c0001t0005g0014 a0001c0001t0005g0196 others(8): Show |
11 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.1205+165C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83598888 | |||||||
chr4:83599082 | C | A | 83 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(80): Show |
84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1205+359C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599082 | |||||||
chr4:83599524 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1205+801T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599524 | |||||||
chr4:83599534 | T | G | 188 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1205+811T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599534 | |||||||
chr4:83599545 | C | G | 188 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1205+822C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599545 | |||||||
chr4:83599864 | T | G | 1 | a0001c0001t0002g0258 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1205+1141T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599864 | |||||||
chr4:83599865 | G | T | 1 | a0001c0001t0002g0258 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1205+1142G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599865 | |||||||
chr4:83599948 | A | G | 3 | a0001c0001t0001g0238 a0001c0001t0001g0240 a0001c0001t0001g0241 |
3 | NA18939.hp2 NA19011.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1205+1225A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599948 | |||||||
chr4:83599963 | T | C | 11 | a0001c0001t0003g0183 a0001c0001t0003g0197 a0001c0001t0005g0182 others(8): Show |
11 | HG00099.hp1 HG02258.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1205+1240T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83599963 | |||||||
chr4:83600124 | A | C | 199 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(196): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1205+1401A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600124 | |||||||
chr4:83600131 | T | C | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1205+1408T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600131 | |||||||
chr4:83600328 | C | CCAT | 177 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(174): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1205+1606_1205+160 others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83600328 | ||||||
chr4:83600330 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1205+1607A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600330 | |||||||
chr4:83600385 | A | G | 7 | a0001c0001t0003g0183 a0001c0001t0005g0182 a0001c0001t0005g0205 others(4): Show |
7 | HG00099.hp1 HG02258.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1205+1662A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600385 | |||||||
chr4:83600479 | T | C | 72 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1205+1756T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600479 | |||||||
chr4:83600503 | A | AATT | 177 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(174): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1205+1796_1205+179 others(7): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83600503 | ||||||
chr4:83600531 | G | A | 1 | a0001c0001t0005g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1205+1808G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600531 | |||||||
chr4:83600621 | G | C | 3 | a0001c0001t0003g0081 a0001c0001t0003g0175 a0001c0001t0003g0218 |
3 | HG00280.hp2 HG01081.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1205+1898G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600621 | |||||||
chr4:83600664 | A | G | 178 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(175): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1205+1941A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600664 | |||||||
chr4:83600669 | A | AT | 11 | a0001c0001t0003g0001 a0001c0001t0003g0047 a0001c0001t0003g0048 others(8): Show |
12 | HG01109.hp2 HG01175.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.1205+1954dupT | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83600669 | ||||||
chr4:83600694 | T | C | 204 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0002g0007 others(201): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1205+1971T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600694 | |||||||
chr4:83600827 | C | T | 1 | a0003c0003t0002g0284 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1205+2104C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600827 | |||||||
chr4:83600927 | T | G | 6 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1205+2204T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83600927 | |||||||
chr4:83601021 | C | T | 3 | a0001c0001t0002g0226 a0001c0001t0002g0311 a0001c0001t0002g0312 |
3 | HG01884.hp1 HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1205+2298C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601021 | |||||||
chr4:83601438 | G | T | 1 | a0001c0001t0002g0329 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1205+2715G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601438 | |||||||
chr4:83601564 | G | A | 17 | a0001c0001t0005g0004 a0001c0001t0005g0012 a0001c0001t0005g0014 others(14): Show |
17 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.1205+2841G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601564 | |||||||
chr4:83601624 | G | A | 4 | a0001c0001t0006g0002 a0001c0001t0006g0003 a0001c0001t0006g0206 others(1): Show |
4 | HG01891.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1205+2901G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601624 | |||||||
chr4:83601631 | T | C | 2 | a0001c0001t0004g0019 a0001c0001t0004g0227 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1205+2908T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601631 | |||||||
chr4:83601647 | C | T | 1 | a0001c0001t0002g0268 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1205+2924C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601647 | |||||||
chr4:83601731 | G | C | 1 | a0001c0001t0003g0197 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1206-2937G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601731 | |||||||
chr4:83601740 | C | T | 103 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(100): Show |
103 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1206-2928C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601740 | |||||||
chr4:83601876 | T | C | 1 | a0001c0001t0005g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1206-2792T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601876 | |||||||
chr4:83601949 | T | C | 206 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1206-2719T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601949 | |||||||
chr4:83601950 | C | G | 1 | a0001c0001t0002g0258 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1206-2718C>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83601950 | |||||||
chr4:83602019 | T | C | 1 | a0001c0001t0006g0212 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1206-2649T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602019 | |||||||
chr4:83602075 | A | T | 1 | a0003c0003t0002g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1206-2593A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602075 | |||||||
chr4:83602118 | A | G | 8 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(5): Show |
8 | HG02258.hp2 HG02622.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1206-2550A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602118 | |||||||
chr4:83602122 | G | T | 1 | a0001c0001t0003g0041 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1206-2546G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602122 | |||||||
chr4:83602162 | T | A | 1 | a0001c0001t0005g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1206-2506T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602162 | |||||||
chr4:83602467 | T | G | 1 | a0001c0001t0003g0041 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1206-2201T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602467 | |||||||
chr4:83602557 | AAG | A | 73 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(70): Show |
74 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1206-2109_1206-210 others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83602557 | ||||||
chr4:83602588 | G | C | 1 | a0001c0001t0005g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1206-2080G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602588 | |||||||
chr4:83602613 | TA | T | 187 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(184): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1206-2053delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83602613 | ||||||
chr4:83602766 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1206-1902C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83602766 | |||||||
chr4:83603037 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1206-1631G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603037 | |||||||
chr4:83603330 | C | A | 71 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(68): Show |
72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1206-1338C>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603330 | |||||||
chr4:83603439 | A | G | 206 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1206-1229A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603439 | |||||||
chr4:83603470 | C | T | 176 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(173): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1206-1198C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603470 | |||||||
chr4:83603589 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1206-1079G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603589 | |||||||
chr4:83603647 | G | A | 2 | a0001c0001t0002g0258 a0001c0001t0002g0263 |
2 | HG00408.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1206-1021G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603647 | |||||||
chr4:83603739 | AAGATTGT others(28): Show |
A | 1 | a0001c0001t0002g0264 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1206-926_1206-892d others(37): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83603739 | ||||||
chr4:83603790 | C | CA | 12 | a0001c0001t0001g0093 a0001c0001t0001g0122 a0001c0001t0001g0125 others(9): Show |
12 | HG01261.hp1 HG02027.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1206-856dupA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83603790 | ||||||
chr4:83603790 | CA | C | 19 | a0001c0001t0001g0116 a0001c0001t0001g0152 a0001c0001t0001g0155 others(16): Show |
19 | HG01346.hp1 HG01993.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1206-856delA | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83603790 | ||||||
chr4:83603790 | CAAA | C | 174 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(171): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1206-858_1206-856d others(5): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83603790 | ||||||
chr4:83603790 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0035 |
3 | HG00741.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1206-865_1206-856d others(12): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83603790 | ||||||
chr4:83603804 | A | C | 176 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(173): Show |
177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1206-864A>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603804 | |||||||
chr4:83603907 | A | G | 13 | a0001c0001t0005g0012 a0001c0001t0005g0014 a0001c0001t0005g0196 others(10): Show |
13 | HG02809.hp1 HG02818.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.1206-761A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603907 | |||||||
chr4:83603986 | A | G | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-682A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603986 | |||||||
chr4:83603991 | A | T | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-677A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603991 | |||||||
chr4:83603999 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-669G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83603999 | |||||||
chr4:83604000 | T | A | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-668T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604000 | |||||||
chr4:83604021 | G | T | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-647G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604021 | |||||||
chr4:83604023 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-645G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604023 | |||||||
chr4:83604045 | T | A | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-623T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604045 | |||||||
chr4:83604048 | T | C | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-620T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604048 | |||||||
chr4:83604050 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-618G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604050 | |||||||
chr4:83604055 | A | T | 73 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(70): Show |
74 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1206-613A>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604055 | |||||||
chr4:83604063 | T | TTTTG | 3 | a0001c0001t0004g0031 a0001c0001t0004g0032 a0001c0001t0004g0033 |
3 | HG02145.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1206-585_1206-582d others(6): Show |
GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr4 | 83604063 | ||||||
chr4:83604065 | T | A | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-603T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604065 | |||||||
chr4:83604067 | G | T | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-601G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604067 | |||||||
chr4:83604070 | T | C | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-598T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604070 | |||||||
chr4:83604071 | G | T | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-597G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604071 | |||||||
chr4:83604075 | G | T | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-593G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604075 | |||||||
chr4:83604083 | G | T | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-585G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604083 | |||||||
chr4:83604093 | C | T | 103 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(100): Show |
103 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1206-575C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604093 | |||||||
chr4:83604094 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-574G>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604094 | |||||||
chr4:83604095 | A | G | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-573A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604095 | |||||||
chr4:83604112 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-556C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604112 | |||||||
chr4:83604128 | A | G | 72 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0006 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1206-540A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604128 | |||||||
chr4:83604134 | T | A | 1 | a0001c0001t0003g0026 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1206-534T>A | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604134 | |||||||
chr4:83604141 | G | T | 1 | a0001c0001t0002g0328 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1206-527G>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604141 | |||||||
chr4:83604142 | G | C | 1 | a0001c0001t0002g0328 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1206-526G>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604142 | |||||||
chr4:83604163 | C | T | 1 | a0001c0001t0004g0013 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1206-505C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604163 | |||||||
chr4:83604220 | C | T | 1 | a0001c0001t0005g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1206-448C>T | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604220 | |||||||
chr4:83604228 | T | G | 103 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(100): Show |
103 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.1206-440T>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604228 | |||||||
chr4:83604270 | T | C | 206 | a0001c0001t0002g0007 a0001c0001t0002g0009 a0001c0001t0002g0010 others(203): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1206-398T>C | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604270 | |||||||
chr4:83604554 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0116 a0001c0001t0001g0166 |
3 | HG01346.hp1 HG01981.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1206-114A>G | GPAT3 | ENSG00000138678.11 | transcript | ENST00000264409.5 | protein_coding | 11/11 | chr4 | 83604554 |