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
3551 BAA01g02780 A01 1294710 G A missense_variant MODERATE c.7204G>A|p.Glu2402Lys S136
3552 BAA01g02780 A01 1294875 C T synonymous_variant LOW c.7278C>T|p.Leu2426Leu S262
3553 BAA01g02780 A01 1295311 C T intron_variant MODIFIER c.7680+34C>T| S88
3554 BAA01g02780 A01 1295546 G A synonymous_variant LOW c.7788G>A|p.Lys2596Lys S103
3555 BAA01g02780 A01 1296612 C T missense_variant MODERATE c.8854C>T|p.Leu2952Phe S231
3556 BAA01g02780 A01 1297458 C T synonymous_variant LOW c.9291C>T|p.Cys3097Cys S221
3557 BAA01g02780 A01 1297529 G A missense_variant MODERATE c.9362G>A|p.Ser3121Asn S157
S163
3558 BAA01g02780 A01 1298493 G A missense_variant MODERATE c.10063G>A|p.Gly3355Ser S123
3559 BAA01g02780 A01 1298503 G A missense_variant MODERATE c.10073G>A|p.Arg3358Lys S136
S15
S156
S2
S3
S4
S6
3560 BAA01g02780 A01 1298911 C T splice_region_variant&intron_variant LOW c.10345-3C>T| S133
3561 BAA01g02800 A01 1303855 C T synonymous_variant LOW c.1656C>T|p.Val552Val S211
S227
3562 BAA01g02820 A01 1307832 C T upstream_gene_variant MODIFIER c.-1478C>T| S51
3563 BAA01g02820 A01 1309338 G A missense_variant MODERATE c.29G>A|p.Arg10Lys S37
3564 BAA01g02820 A01 1309395 C T missense_variant MODERATE c.86C>T|p.Pro29Leu S139
3565 BAA01g02830 A01 1310192 G A upstream_gene_variant MODIFIER c.-2009G>A| S98
3566 BAA01g02830 A01 1312382 G A missense_variant MODERATE c.182G>A|p.Arg61His S136
3567 BAA01g02830 A01 1312482 C T synonymous_variant LOW c.282C>T|p.Asp94Asp S35
3568 BAA01g02830 A01 1312605 C T synonymous_variant LOW c.405C>T|p.Tyr135Tyr S267
3569 BAA01g02850 A01 1313101 C T upstream_gene_variant MODIFIER c.-3119C>T| S212
3570 BAA01g02850 A01 1313973 G A upstream_gene_variant MODIFIER c.-2247G>A| S262
3571 BAA01g02850 A01 1314756 G A upstream_gene_variant MODIFIER c.-1464G>A| S199
3572 BAA01g02850 A01 1315213 G A upstream_gene_variant MODIFIER c.-1007G>A| S276
3573 BAA01g02860 A01 1317302 C T missense_variant MODERATE c.578G>A|p.Gly193Glu S203
3574 BAA01g02860 A01 1317303 C T missense_variant MODERATE c.577G>A|p.Gly193Arg S150
3575 BAA01g02840 A01 1317832 C T upstream_gene_variant MODIFIER c.-1855G>A| S170