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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g16660 A10 16348419 G A missense_variant MODERATE c.1568C>T|p.Pro523Leu S151
S257
S262
S263
2 BAA10g16660 A10 16348850 C T intron_variant MODIFIER c.1213+30G>A| S210
S225
3 BAA10g16660 A10 16348991 C T missense_variant MODERATE c.1102G>A|p.Asp368Asn S23
4 BAA10g16660 A10 16349142 G A synonymous_variant LOW c.1044C>T|p.Tyr348Tyr S128
5 BAA10g16660 A10 16349306 G A missense_variant MODERATE c.880C>T|p.Pro294Ser S43
6 BAA10g16660 A10 16350394 C T intron_variant MODIFIER c.688-694G>A| S60
7 BAA10g16660 A10 16350433 C T intron_variant MODIFIER c.688-733G>A| S162
8 BAA10g16660 A10 16350455 G A intron_variant MODIFIER c.688-755C>T| S207
9 BAA10g16660 A10 16350718 G A intron_variant MODIFIER c.688-1018C>T| S105
S106
10 BAA10g16660 A10 16350826 G A intron_variant MODIFIER c.688-1126C>T| S110
11 BAA10g16660 A10 16351075 G A intron_variant MODIFIER c.688-1375C>T| S67
12 BAA10g16660 A10 16352299 C T intron_variant MODIFIER c.688-2599G>A| S301
S304
13 BAA10g16660 A10 16352770 G A intron_variant MODIFIER c.688-3070C>T| S219
14 BAA10g16660 A10 16352786 G A intron_variant MODIFIER c.688-3086C>T| S155
S211
15 BAA10g16660 A10 16358063 C T missense_variant MODERATE c.460G>A|p.Glu154Lys S46
16 BAA10g16660 A10 16359047 G A missense_variant MODERATE c.127C>T|p.Leu43Phe S72
S78
17 BAA10g16660 A10 16359472 C T upstream_gene_variant MODIFIER c.-299G>A| S174
18 BAA10g16660 A10 16360597 C T upstream_gene_variant MODIFIER c.-1424G>A| S11
19 BAA10g16660 A10 16362779 C T upstream_gene_variant MODIFIER c.-3606G>A| S10
20 BAA10g16660 A10 16362943 G A upstream_gene_variant MODIFIER c.-3770C>T| S125
21 BAA10g16660 A10 16362974 C T upstream_gene_variant MODIFIER c.-3801G>A| S211
S227
22 BAA10g16660 A10 16363097 G A upstream_gene_variant MODIFIER c.-3924C>T| S165