Colon Cancer: Gene >> B4GALT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319769
Start	161171884:161171884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114C>T
AA Mutation	p.Arg372Cys(p.R372C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319769
Start	161172234:161172234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.901C>T
AA Mutation	p.Pro301Ser(p.P301S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319769
Start	161173904:161173904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748981503
CDS Mutation	c.635G>A
AA Mutation	p.Arg212Gln(p.R212Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319769
Start	161173693:161173693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715G>T
AA Mutation	p.Ala239Ser(p.A239S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319769
Start	161175025:161175025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457C>A
AA Mutation	p.Gln153Lys(p.Q153K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319769
Start	161175930:161175930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367870203
CDS Mutation	c.131C>T
AA Mutation	p.Pro44Leu(p.P44L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319769
Start	161173905:161173905(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.634delC
AA Mutation	p.Arg212GlyfsTer10(p.R212Gfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> B4GALT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319769
Start	161175930:161175930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367870203
CDS Mutation	c.131C>T
AA Mutation	p.Pro44Leu(p.P44L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319769
Start	161176053:161176053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375294931
CDS Mutation	c.8G>A
AA Mutation	p.Arg3Gln(p.R3Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319769
Start	161175139:161175139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775570899
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Cys(p.R115C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript