Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CMAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22061320:22061320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828A>C
AA Mutation	p.Lys276Asn(p.K276N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22046553:22046553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250G>A
AA Mutation	p.Ala84Thr(p.A84T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22060898:22060898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760T>C
AA Mutation	p.Trp254Arg(p.W254R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22046443:22046443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140C>T
AA Mutation	p.Ala47Val(p.A47V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22055241:22055241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353A>T
AA Mutation	p.Asp118Val(p.D118V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22055575:22055575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199957467
CDS Mutation	c.524G>A
AA Mutation	p.Arg175His(p.R175H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22055217:22055217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753560501
CDS Mutation	c.329G>A
AA Mutation	p.Arg110Gln(p.R110Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229329
Start	22065305:22065305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1299A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000229329
Start	22065311:22065311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CMAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22055160:22055160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272C>T
AA Mutation	p.Ser91Leu(p.S91L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22055530:22055530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479T>G
AA Mutation	p.Met160Arg(p.M160R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22055217:22055217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753560501
CDS Mutation	c.329G>A
AA Mutation	p.Arg110Gln(p.R110Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22061312:22061312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.820G>A
AA Mutation	p.Glu274Lys(p.E274K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22065148:22065148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142T>C
AA Mutation	p.Leu381Ser(p.L381S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000229329
Start	22061411:22061411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189328375
CDS Mutation	c.919G>T
AA Mutation	p.Asp307Tyr(p.D307Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript