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


Gene ID

Results: 1 - 47 of 47 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g33350 A06 22547695 G A downstream_gene_variant MODIFIER c.*4377C>T| S209
2 BAA06g33350 A06 22548475 C T downstream_gene_variant MODIFIER c.*3597G>A| S96
3 BAA06g33350 A06 22548857 C T downstream_gene_variant MODIFIER c.*3215G>A| S302
4 BAA06g33350 A06 22549058 G A downstream_gene_variant MODIFIER c.*3014C>T| S273
5 BAA06g33350 A06 22551517 G A downstream_gene_variant MODIFIER c.*555C>T| S219
6 BAA06g33350 A06 22551800 G A downstream_gene_variant MODIFIER c.*272C>T| S298
7 BAA06g33350 A06 22552014 C T downstream_gene_variant MODIFIER c.*58G>A| S112
8 BAA06g33350 A06 22552164 C T missense_variant MODERATE c.10270G>A|p.Glu3424Lys S286
9 BAA06g33350 A06 22552270 C T synonymous_variant LOW c.10164G>A|p.Gln3388Gln S288
10 BAA06g33350 A06 22552293 C T missense_variant MODERATE c.10141G>A|p.Asp3381Asn S82
S92
11 BAA06g33350 A06 22552331 C T missense_variant MODERATE c.10103G>A|p.Cys3368Tyr S62
12 BAA06g33350 A06 22552592 G A missense_variant MODERATE c.9842C>T|p.Pro3281Leu S20
13 BAA06g33350 A06 22553249 G A intron_variant MODIFIER c.9496-39C>T| S305
14 BAA06g33350 A06 22553356 G A synonymous_variant LOW c.9432C>T|p.Leu3144Leu S284
15 BAA06g33350 A06 22553402 C T missense_variant&splice_region_variant MODERATE c.9386G>A|p.Ser3129Asn S6
16 BAA06g33350 A06 22554042 G A intron_variant MODIFIER c.9132+189C>T| S233
17 BAA06g33350 A06 22554631 G A synonymous_variant LOW c.8820C>T|p.Leu2940Leu S37
18 BAA06g33350 A06 22556110 G A missense_variant MODERATE c.8042C>T|p.Thr2681Met S268
19 BAA06g33350 A06 22557857 G A synonymous_variant LOW c.7017C>T|p.Ser2339Ser S185
20 BAA06g33350 A06 22558537 G A missense_variant MODERATE c.6523C>T|p.Pro2175Ser S125
S268
21 BAA06g33350 A06 22558854 G A intron_variant MODIFIER c.6286-80C>T| S2
22 BAA06g33350 A06 22559180 G A missense_variant MODERATE c.6230C>T|p.Ser2077Phe S273
23 BAA06g33350 A06 22559269 C T intron_variant MODIFIER c.6213+9G>A| S116
24 BAA06g33350 A06 22559997 C T missense_variant MODERATE c.5579G>A|p.Gly1860Glu S112
25 BAA06g33350 A06 22560751 G A intron_variant MODIFIER c.5361+27C>T| S256