Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IGF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307046
Start	102475730:102475730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133T>G
AA Mutation	p.Ser45Ala(p.S45A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307046
Start	102419517:102419517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394A>G
AA Mutation	p.Thr132Ala(p.T132A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307046
Start	102417992:102417992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307046
Start	102475713:102475713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373202198
CDS Mutation	c.150G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307046
Start	102475671:102475671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760590942
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307046
Start	102419584:102419584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778994665
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307046
Start	102417827:102417827(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.579delA
AA Mutation	p.Gly194GlufsTer8(p.G194Efs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IGF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307046
Start	102475706:102475706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157C>T
AA Mutation	p.Leu53Phe(p.L53F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307046
Start	102475671:102475671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760590942
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript