Colon Cancer: Gene >> SAMD14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330175
Start	50114200:50114200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929A>C
AA Mutation	p.Gln310Pro(p.Q310P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330175
Start	50118246:50118246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200210474
CDS Mutation	c.125G>A
AA Mutation	p.Arg42Gln(p.R42Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330175
Start	50115894:50115894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369339604
CDS Mutation	c.598C>T
AA Mutation	p.Arg200Cys(p.R200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330175
Start	50117658:50117658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.248G>A
AA Mutation	p.Arg83His(p.R83H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330175
Start	50115857:50115857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635G>A
AA Mutation	p.Gly212Asp(p.G212D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330175
Start	50113005:50113005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778713639
CDS Mutation	c.1142G>A
AA Mutation	p.Arg381His(p.R381H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330175
Start	50116025:50116025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565C>T
AA Mutation	p.Arg189Cys(p.R189C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330175
Start	50114274:50114274(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.855delC
AA Mutation	p.Ser286AlafsTer67(p.S286Afs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000330175
Start	50116091:50116091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SAMD14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330175
Start	50124952:50124952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8C>A
AA Mutation	p.Ser3Tyr(p.S3Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript