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


Gene ID

Results: 1 - 27 of 27 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g15600 A10 15915410 G A missense_variant MODERATE c.2363C>T|p.Thr788Ile S217
S248
2 BAA10g15600 A10 15915623 C T missense_variant MODERATE c.2150G>A|p.Arg717Gln S180
3 BAA10g15600 A10 15917640 C T intron_variant MODIFIER c.1893-1760G>A| S12
4 BAA10g15600 A10 15918014 G A intron_variant MODIFIER c.1893-2134C>T| S77
5 BAA10g15600 A10 15918056 G A intron_variant MODIFIER c.1893-2176C>T| S245
6 BAA10g15600 A10 15919207 C T intron_variant MODIFIER c.1893-3327G>A| S301
S304
7 BAA10g15600 A10 15919593 C T intron_variant MODIFIER c.1893-3713G>A| S249
8 BAA10g15600 A10 15920196 G A intron_variant MODIFIER c.1892+3432C>T| S174
S27
9 BAA10g15600 A10 15920293 C T intron_variant MODIFIER c.1892+3335G>A| S282
10 BAA10g15600 A10 15920460 C T intron_variant MODIFIER c.1892+3168G>A| S131
11 BAA10g15600 A10 15924101 A G synonymous_variant LOW c.1419T>C|p.Pro473Pro S6
12 BAA10g15600 A10 15925663 C T missense_variant MODERATE c.490G>A|p.Glu164Lys S247
13 BAA10g15600 A10 15925749 G A missense_variant MODERATE c.404C>T|p.Ser135Phe S205
14 BAA10g15600 A10 15926926 C T intron_variant MODIFIER c.218-991G>A| S233
15 BAA10g15600 A10 15926957 C T intron_variant MODIFIER c.218-1022G>A| S105
S106
16 BAA10g15600 A10 15927989 G A intron_variant MODIFIER c.218-2054C>T| S284
17 BAA10g15600 A10 15928175 G A intron_variant MODIFIER c.218-2240C>T| S17
18 BAA10g15600 A10 15928588 G A intron_variant MODIFIER c.217+2052C>T| S53
19 BAA10g15600 A10 15928642 G T intron_variant MODIFIER c.217+1998C>A| S16
S26
S294
S37
S99
20 BAA10g15600 A10 15928648 C T intron_variant MODIFIER c.217+1992G>A| S8
21 BAA10g15600 A10 15928723 G A intron_variant MODIFIER c.217+1917C>T| S293
22 BAA10g15600 A10 15928878 G A intron_variant MODIFIER c.217+1762C>T| S34
23 BAA10g15600 A10 15929319 C T intron_variant MODIFIER c.217+1321G>A| S78
24 BAA10g15600 A10 15930640 C T missense_variant&splice_region_variant MODERATE c.217G>A|p.Ala73Thr S78
25 BAA10g15600 A10 15931285 C T upstream_gene_variant MODIFIER c.-429G>A| S299