Colon Cancer: Gene >> B3GNT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287590
Start	231397934:231397934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199641918
CDS Mutation	c.215C>T
AA Mutation	p.Thr72Met(p.T72M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287590
Start	231397870:231397870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>T
AA Mutation	p.Pro51Ser(p.P51S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287590
Start	231398855:231398855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781471024
CDS Mutation	c.1136C>T
AA Mutation	p.Pro379Leu(p.P379L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287590
Start	231397741:231397741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367701147
CDS Mutation	c.22G>A
AA Mutation	p.Val8Ile(p.V8I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287590
Start	231398636:231398636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.917C>T
AA Mutation	p.Ala306Val(p.A306V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287590
Start	231398603:231398603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751482955
CDS Mutation	c.884C>T
AA Mutation	p.Pro295Leu(p.P295L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287590
Start	231397776:231397776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748391272
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287590
Start	231398463:231398463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> B3GNT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287590
Start	231398116:231398116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397G>A
AA Mutation	p.Asp133Asn(p.D133N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287590
Start	231398537:231398537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818G>T
AA Mutation	p.Arg273Leu(p.R273L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287590
Start	231398323:231398323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604G>A
AA Mutation	p.Asp202Asn(p.D202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287590
Start	231397968:231397968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript