Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GALNT12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375011
Start	98831950:98831950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910G>A
AA Mutation	p.Val304Ile(p.V304I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375011
Start	98848981:98848981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1635G>T
AA Mutation	p.Lys545Asn(p.K545N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375011
Start	98844206:98844206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1455T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375011
Start	98831835:98831835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774616588
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375011
Start	98849023:98849023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112898261
CDS Mutation	c.1677C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375011
Start	98844182:98844182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746070097
CDS Mutation	c.1431C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000375011
Start	98823331:98823331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.447G>A
AA Mutation	p.Trp149Ter(p.W149*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GALNT12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375011
Start	98837080:98837080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1144C>T
AA Mutation	p.Arg382Cys(p.R382C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375011
Start	98849013:98849013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774534357
CDS Mutation	c.1667G>A
AA Mutation	p.Ser556Asn(p.S556N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375011
Start	98846089:98846089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1571C>A
AA Mutation	p.Thr524Asn(p.T524N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375011
Start	98848999:98848999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776668170
CDS Mutation	c.1653G>A
Mutation Classification	Silent
Feature Type	Transcript