Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
8001 BAA01g06440 A01 2865690 G A stop_gained HIGH c.3265C>T|p.Arg1089* S298
8002 BAA01g06440 A01 2865799 G A intron_variant MODIFIER c.3219-63C>T| S284
8003 BAA01g06440 A01 2865925 G A intron_variant MODIFIER c.3218+12C>T| S57
8004 BAA01g06440 A01 2866119 G A intron_variant MODIFIER c.3049-13C>T| S116
8005 BAA01g06440 A01 2866204 C T intron_variant MODIFIER c.3048+11G>A| S130
8006 BAA01g06440 A01 2866733 G A missense_variant MODERATE c.2716C>T|p.Leu906Phe S28
8007 BAA01g06440 A01 2866872 G A missense_variant MODERATE c.2665C>T|p.Leu889Phe S142
8008 BAA01g06440 A01 2868383 C T intron_variant MODIFIER c.1981+28G>A| S148
S210
S30
S31
8009 BAA01g06440 A01 2868966 C T intron_variant MODIFIER c.1604+50G>A| S132
S137
S215
S89
8010 BAA01g06440 A01 2869128 G A missense_variant MODERATE c.1492C>T|p.Arg498Cys S219
8011 BAA01g06440 A01 2869438 G A intron_variant MODIFIER c.1447-265C>T| S199
8012 BAA01g06440 A01 2869721 C T intron_variant MODIFIER c.1447-548G>A| S130
8013 BAA01g06440 A01 2870728 C T intron_variant MODIFIER c.1446+1023G>A| S100
8014 BAA01g06440 A01 2871134 C T intron_variant MODIFIER c.1446+617G>A| S153
S213
8015 BAA01g06440 A01 2871151 G A intron_variant MODIFIER c.1446+600C>T| S129
8016 BAA01g06440 A01 2871295 G A intron_variant MODIFIER c.1446+456C>T| S209
8017 BAA01g06440 A01 2871342 C T intron_variant MODIFIER c.1446+409G>A| S36
8018 BAA01g06440 A01 2871453 C T intron_variant MODIFIER c.1446+298G>A| S255
8019 BAA01g06440 A01 2871496 G A intron_variant MODIFIER c.1446+255C>T| S23
8020 BAA01g06440 A01 2871540 A T intron_variant MODIFIER c.1446+211T>A| S98
8021 BAA01g06440 A01 2871603 C T intron_variant MODIFIER c.1446+148G>A| S46
8022 BAA01g06440 A01 2872273 G A intron_variant MODIFIER c.1079-155C>T| S191
8023 BAA01g06440 A01 2872408 C T intron_variant MODIFIER c.1079-290G>A| S164
8024 BAA01g06440 A01 2872526 C T intron_variant MODIFIER c.1079-408G>A| S263
8025 BAA01g06440 A01 2872908 G A intron_variant MODIFIER c.1078+238C>T| S208
S219