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


Gene ID

Results: 1 - 39 of 39 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g07920 A07 17087057 C T intron_variant MODIFIER c.789+63G>A| S114
2 BAA07g07920 A07 17088326 C T intron_variant MODIFIER c.720-1137G>A| S200
3 BAA07g07920 A07 17089722 C T intron_variant MODIFIER c.720-2533G>A| S169
4 BAA07g07920 A07 17089941 G A intron_variant MODIFIER c.720-2752C>T| S210
5 BAA07g07920 A07 17090375 G A intron_variant MODIFIER c.720-3186C>T| S208
6 BAA07g07920 A07 17090519 C T intron_variant MODIFIER c.720-3330G>A| S18
7 BAA07g07920 A07 17090791 G A intron_variant MODIFIER c.720-3602C>T| S57
8 BAA07g07920 A07 17092040 G A intron_variant MODIFIER c.719+4178C>T| S240
9 BAA07g07920 A07 17092056 G A intron_variant MODIFIER c.719+4162C>T| S229
10 BAA07g07920 A07 17092158 C T intron_variant MODIFIER c.719+4060G>A| S232
11 BAA07g07920 A07 17092704 G A intron_variant MODIFIER c.719+3514C>T| S190
12 BAA07g07920 A07 17093076 G A intron_variant MODIFIER c.719+3142C>T| S157
S163
13 BAA07g07920 A07 17093329 C T intron_variant MODIFIER c.719+2889G>A| S150
14 BAA07g07920 A07 17093384 C T intron_variant MODIFIER c.719+2834G>A| S217
S248
15 BAA07g07920 A07 17095450 G T intron_variant MODIFIER c.719+768C>A| S196
16 BAA07g07920 A07 17095942 G A intron_variant MODIFIER c.719+276C>T| S28
17 BAA07g07920 A07 17096009 C T intron_variant MODIFIER c.719+209G>A| S178
18 BAA07g07920 A07 17096051 C T intron_variant MODIFIER c.719+167G>A| S259
19 BAA07g07920 A07 17096577 C T intron_variant MODIFIER c.627-267G>A| S192
20 BAA07g07920 A07 17097235 C T intron_variant MODIFIER c.627-925G>A| S217
21 BAA07g07920 A07 17099026 G A intron_variant MODIFIER c.626+2644C>T| S12
22 BAA07g07920 A07 17100007 C T intron_variant MODIFIER c.626+1663G>A| S11
23 BAA07g07920 A07 17100994 G A intron_variant MODIFIER c.626+676C>T| S168
24 BAA07g07920 A07 17100998 C T intron_variant MODIFIER c.626+672G>A| S157
S166
S167
S262
S263
25 BAA07g07920 A07 17101057 T A intron_variant MODIFIER c.626+613A>T| S16