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
701 BAA01g00520 A01 246251 G A missense_variant MODERATE c.763G>A|p.Glu255Lys S242
702 BAA01g00520 A01 246345 G A missense_variant MODERATE c.857G>A|p.Gly286Asp S234
703 BAA01g00520 A01 247300 G A synonymous_variant LOW c.1812G>A|p.Thr604Thr S274
704 BAA01g00520 A01 249881 C T missense_variant MODERATE c.2698C>T|p.Leu900Phe S282
705 BAA01g00520 A01 250010 G A missense_variant MODERATE c.2827G>A|p.Val943Ile S136
706 BAA01g00520 A01 250111 C T synonymous_variant LOW c.2928C>T|p.Leu976Leu S46
707 BAA01g00520 A01 250717 C T synonymous_variant LOW c.3358C>T|p.Leu1120Leu S236
708 BAA01g00520 A01 250880 G A missense_variant MODERATE c.3521G>A|p.Arg1174Lys S37
709 BAA01g00520 A01 251098 G A intron_variant MODIFIER c.3534+205G>A| S78
710 BAA01g00520 A01 251224 C T intron_variant MODIFIER c.3535-166C>T| S171
711 BAA01g00520 A01 251321 C T intron_variant MODIFIER c.3535-69C>T| S58
712 BAA01g00520 A01 251780 C T missense_variant MODERATE c.3925C>T|p.Leu1309Phe S38
713 BAA01g00520 A01 251783 C T synonymous_variant LOW c.3928C>T|p.Leu1310Leu S75
S81
714 BAA01g00520 A01 252089 C T intron_variant MODIFIER c.4176+58C>T| S158
715 BAA01g00520 A01 252356 C T missense_variant MODERATE c.4376C>T|p.Thr1459Ile S68
716 BAA01g00520 A01 252435 G A synonymous_variant LOW c.4455G>A|p.Gln1485Gln S96
717 BAA01g00520 A01 252535 C T synonymous_variant LOW c.4555C>T|p.Leu1519Leu S11
718 BAA01g00520 A01 253300 G A intron_variant MODIFIER c.4875+21G>A| S165
719 BAA01g00520 A01 254128 G A missense_variant MODERATE c.5378G>A|p.Ser1793Asn S289
S290
720 BAA01g00520 A01 254307 G A missense_variant MODERATE c.5557G>A|p.Val1853Ile S131
721 BAA01g00520 A01 254770 G A missense_variant MODERATE c.5834G>A|p.Gly1945Glu S10
S230
722 BAA01g00520 A01 255262 C T missense_variant MODERATE c.6179C>T|p.Thr2060Ile S305
723 BAA01g00520 A01 256549 C T intron_variant MODIFIER c.6903+235C>T| S113
724 BAA01g00520 A01 256639 G A intron_variant MODIFIER c.6904-213G>A| S183
S198
725 BAA01g00520 A01 256643 G A intron_variant MODIFIER c.6904-209G>A| S169