Colon Cancer: Gene >> GAS7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000432992
Start	9934203:9934203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779042022
CDS Mutation	c.848C>T
AA Mutation	p.Ala283Val(p.A283V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000432992
Start	9919681:9919681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1163A>G
AA Mutation	p.Asp388Gly(p.D388G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000432992
Start	10198266:10198266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125G>A
AA Mutation	p.Gly42Asp(p.G42D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000432992
Start	9969748:9969748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400G>A
AA Mutation	p.Ala134Thr(p.A134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000432992
Start	9926678:9926678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.977G>A
AA Mutation	p.Arg326His(p.R326H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000432992
Start	9917283:9917283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1376T>G
AA Mutation	p.Leu459Arg(p.L459R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000432992
Start	9981874:9981874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315G>C
AA Mutation	p.Trp105Cys(p.W105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000432992
Start	9919690:9919690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154G>A
AA Mutation	p.Arg385His(p.R385H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432992
Start	9926761:9926761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432992
Start	9969749:9969749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750475073
CDS Mutation	c.399C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432992
Start	9946921:9946921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772183594
CDS Mutation	c.588C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GAS7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000432992
Start	9925595:9925595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019G>A
AA Mutation	p.Arg340Gln(p.R340Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript