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


Gene ID

Results: 1 - 34 of 34 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g42750 A07 36936348 C T missense_variant MODERATE c.5863G>A|p.Ala1955Thr S203
2 BAA07g42750 A07 36940830 C T intron_variant MODIFIER c.4223+17G>A| S148
S30
S31
3 BAA07g42750 A07 36940928 C T missense_variant MODERATE c.4142G>A|p.Gly1381Glu S148
S30
S31
4 BAA07g42750 A07 36941198 C T synonymous_variant LOW c.3960G>A|p.Pro1320Pro S118
5 BAA07g42750 A07 36941957 C T missense_variant MODERATE c.3383G>A|p.Gly1128Asp S2
6 BAA07g42750 A07 36942148 C T intron_variant MODIFIER c.3286-94G>A| S73
S91
7 BAA07g42750 A07 36943676 G A intron_variant MODIFIER c.3285+709C>T| S171
8 BAA07g42750 A07 36944001 G A intron_variant MODIFIER c.3285+384C>T| S206
S26
9 BAA07g42750 A07 36944315 G A intron_variant MODIFIER c.3285+70C>T| S138
10 BAA07g42750 A07 36944387 C T missense_variant&splice_region_variant MODERATE c.3283G>A|p.Gly1095Arg S277
11 BAA07g42750 A07 36944460 C T synonymous_variant LOW c.3210G>A|p.Ser1070Ser S68
12 BAA07g42750 A07 36944510 C T missense_variant MODERATE c.3160G>A|p.Asp1054Asn S167
13 BAA07g42750 A07 36944563 C T missense_variant MODERATE c.3107G>A|p.Gly1036Asp S56
14 BAA07g42750 A07 36944579 C T missense_variant MODERATE c.3091G>A|p.Glu1031Lys S221
S42
15 BAA07g42750 A07 36945063 C T missense_variant MODERATE c.2607G>A|p.Met869Ile S161
16 BAA07g42750 A07 36945196 G A intron_variant MODIFIER c.2557-83C>T| S33
17 BAA07g42750 A07 36945367 C T intron_variant MODIFIER c.2557-254G>A| S122
18 BAA07g42750 A07 36945915 G A intron_variant MODIFIER c.2557-802C>T| S70
19 BAA07g42750 A07 36946414 G A intron_variant MODIFIER c.2556+496C>T| S138
20 BAA07g42750 A07 36946459 G A intron_variant MODIFIER c.2556+451C>T| S126
21 BAA07g42750 A07 36947630 G A intron_variant MODIFIER c.2485+209C>T| S199
22 BAA07g42750 A07 36947631 T A intron_variant MODIFIER c.2485+208A>T| S199
23 BAA07g42750 A07 36948136 G A synonymous_variant LOW c.2188C>T|p.Leu730Leu S152
24 BAA07g42750 A07 36948151 G A missense_variant MODERATE c.2173C>T|p.Pro725Ser S152
25 BAA07g42750 A07 36949996 C T synonymous_variant LOW c.1029G>A|p.Gly343Gly S173
S176