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
92551 BAA10g02240 A10 1072071 C T missense_variant MODERATE c.835G>A|p.Ala279Thr S252
92552 BAA10g02240 A10 1073023 G A missense_variant MODERATE c.437C>T|p.Ala146Val S60
92553 BAA10g02240 A10 1073413 G A missense_variant MODERATE c.47C>T|p.Thr16Ile S65
92554 BAA10g02230 A10 1073600 G A upstream_gene_variant MODIFIER c.-2581C>T| S82
S92
92555 BAA10g02250 A10 1074522 G A missense_variant MODERATE c.1097C>T|p.Ser366Phe S242
92556 BAA10g02250 A10 1075208 C T synonymous_variant LOW c.411G>A|p.Lys137Lys S308
92557 BAA10g02250 A10 1075524 C T missense_variant MODERATE c.95G>A|p.Gly32Glu S119
92558 BAA10g02260 A10 1075715 G A missense_variant MODERATE c.850C>T|p.Pro284Ser S157
S163
92559 BAA10g02260 A10 1075889 G A splice_region_variant&intron_variant LOW c.792+7C>T| S13
92560 BAA10g02260 A10 1076235 C T synonymous_variant LOW c.453G>A|p.Gly151Gly S116
92561 BAA10g02260 A10 1076684 C T missense_variant MODERATE c.4G>A|p.Val2Ile S56
92562 BAA10g02270 A10 1077976 C T missense_variant MODERATE c.602G>A|p.Gly201Asp S244
92563 BAA10g02270 A10 1078099 C T missense_variant MODERATE c.559G>A|p.Gly187Arg S135
92564 BAA10g02250 A10 1078921 G A upstream_gene_variant MODIFIER c.-3303C>T| S140
92565 BAA10g02250 A10 1079665 C T upstream_gene_variant MODIFIER c.-4047G>A| S275
92566 BAA10g02270 A10 1083940 C T upstream_gene_variant MODIFIER c.-4746G>A| S20
92567 BAA10g02280 A10 1084709 G A missense_variant MODERATE c.1580C>T|p.Thr527Ile S9
92568 BAA10g02280 A10 1084934 C T missense_variant MODERATE c.1355G>A|p.Gly452Glu S87
92569 BAA10g02280 A10 1085193 C T missense_variant MODERATE c.1096G>A|p.Val366Met S233
92570 BAA10g02280 A10 1085407 C T synonymous_variant LOW c.882G>A|p.Ala294Ala S125
92571 BAA10g02280 A10 1085686 C T stop_gained HIGH c.603G>A|p.Trp201* S273
92572 BAA10g02280 A10 1085695 C T synonymous_variant LOW c.594G>A|p.Glu198Glu S6
92573 BAA10g02280 A10 1085971 G A synonymous_variant LOW c.318C>T|p.Leu106Leu S150
92574 BAA10g02290 A10 1086975 C T synonymous_variant LOW c.1023G>A|p.Ser341Ser S287
92575 BAA10g02290 A10 1087070 C T missense_variant MODERATE c.928G>A|p.Val310Ile S247