Colon Cancer: Gene >> SHC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368445
Start	154963813:154963813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780518716
CDS Mutation	c.1742G>A
AA Mutation	p.Arg581Gln(p.R581Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368445
Start	154965684:154965684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1482C>G
AA Mutation	p.Ser494Arg(p.S494R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368445
Start	154970097:154970097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430C>T
AA Mutation	p.Pro144Ser(p.P144S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368445
Start	154970092:154970092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368445
Start	154966414:154966414(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs768690624
CDS Mutation	c.1087delG
AA Mutation	p.Val363TrpfsTer2(p.V363Wfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SHC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368445
Start	154965773:154965773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116278635
CDS Mutation	c.1393G>A
AA Mutation	p.Glu465Lys(p.E465K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript