Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RHD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328664
Start	25284678:25284678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254C>A
AA Mutation	p.Ala85Glu(p.A85E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328664
Start	25301547:25301547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662C>G
AA Mutation	p.Pro221Arg(p.P221R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328664
Start	25301665:25301665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780C>A
AA Mutation	p.His260Gln(p.H260Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328664
Start	25284734:25284734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>T
AA Mutation	p.Gly104Trp(p.G104W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328664
Start	25290711:25290711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406T>A
AA Mutation	p.Leu136Met(p.L136M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328664
Start	25284678:25284678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139501061
CDS Mutation	c.254C>T
AA Mutation	p.Ala85Val(p.A85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328664
Start	25272555:25272555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>A
AA Mutation	p.Ser3Tyr(p.S3Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328664
Start	25303414:25303414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RHD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328664
Start	25301036:25301036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1053352
CDS Mutation	c.577G>A
AA Mutation	p.Glu193Lys(p.E193K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328664
Start	25272653:25272653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201595703
CDS Mutation	c.106G>A
AA Mutation	p.Ala36Thr(p.A36T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328664
Start	25301596:25301596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.711C>A
Mutation Classification	Silent
Feature Type	Transcript