Colon Cancer: Gene >> SCN3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299333
Start	123645666:123645666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140C>T
AA Mutation	p.Ser47Phe(p.S47F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299333
Start	123642475:123642475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770801747
CDS Mutation	c.416G>A
AA Mutation	p.Arg139Gln(p.R139Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299333
Start	123638219:123638219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551T>A
AA Mutation	p.Val184Asp(p.V184D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299333
Start	123642497:123642497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371558196
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Trp(p.R132W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299333
Start	123642520:123642520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201894537
CDS Mutation	c.371G>A
AA Mutation	p.Arg124Gln(p.R124Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299333
Start	123638209:123638209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746888620
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299333
Start	123638253:123638253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760034688
CDS Mutation	c.517C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SCN3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299333
Start	123653790:123653790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12C>A
AA Mutation	p.Phe4Leu(p.F4L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000299333
Start	123645724:123645724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82G>T
AA Mutation	p.Glu28Ter(p.E28*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000299333
Start	123638185:123638185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript