Colon Cancer: Gene >> SDC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339394
Start	30876992:30876992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>A
AA Mutation	p.Val144Met(p.V144M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339394
Start	30878628:30878628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549486633
CDS Mutation	c.251C>T
AA Mutation	p.Ser84Leu(p.S84L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339394
Start	30877105:30877105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556133593
CDS Mutation	c.317C>T
AA Mutation	p.Ala106Val(p.A106V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339394
Start	30874440:30874440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756527724
CDS Mutation	c.1019C>T
AA Mutation	p.Ala340Val(p.A340V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339394
Start	30876760:30876760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780253075
CDS Mutation	c.662C>T
AA Mutation	p.Thr221Met(p.T221M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339394
Start	30874452:30874452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007T>C
AA Mutation	p.Val336Ala(p.V336A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000339394
Start	30877150:30877150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201140173
CDS Mutation	c.272C>T
AA Mutation	p.Ser91Leu(p.S91L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339394
Start	30876963:30876963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SDC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339394
Start	30873311:30873311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767402418
CDS Mutation	c.1229G>A
AA Mutation	p.Arg410His(p.R410H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339394
Start	30874508:30874508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374946441
CDS Mutation	c.951C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339394
Start	30876995:30876995(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.427delC
AA Mutation	p.Leu143TrpfsTer3(p.L143Wfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript