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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g35630 A06 23754208 C T missense_variant MODERATE c.749C>T|p.Ser250Phe S148
S31
2 BAA06g35630 A06 23754333 G A splice_region_variant&synonymous_variant LOW c.783G>A|p.Glu261Glu S69
3 BAA06g35630 A06 23754506 C T synonymous_variant LOW c.861C>T|p.Ser287Ser S34
4 BAA06g35630 A06 23754772 G A missense_variant&splice_region_variant MODERATE c.994G>A|p.Glu332Lys S37
5 BAA06g35630 A06 23756808 G A intron_variant MODIFIER c.1788+49G>A| S65
6 BAA06g35630 A06 23756884 G A intron_variant MODIFIER c.1789-21G>A| S122
7 BAA06g35630 A06 23757282 C T missense_variant MODERATE c.1939C>T|p.Leu647Phe S269
8 BAA06g35630 A06 23757733 C T intron_variant MODIFIER c.2188+41C>T| S43
9 BAA06g35630 A06 23757832 C T synonymous_variant LOW c.2208C>T|p.Asp736Asp S201
10 BAA06g35630 A06 23757896 C T intron_variant MODIFIER c.2232+40C>T| S302
11 BAA06g35630 A06 23757961 C T missense_variant MODERATE c.2252C>T|p.Pro751Leu S68
12 BAA06g35630 A06 23758080 C T intron_variant MODIFIER c.2361+10C>T| S243
S299
13 BAA06g35630 A06 23758398 G A splice_acceptor_variant&intron_variant HIGH c.2494-1G>A| S246
14 BAA06g35630 A06 23758565 G A missense_variant MODERATE c.2572G>A|p.Asp858Asn S239
15 BAA06g35630 A06 23759863 C T missense_variant MODERATE c.3235C>T|p.Leu1079Phe S182