Colon Cancer: Gene >> SULT1A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335715
Start	28592272:28592272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766A>G
AA Mutation	p.Met256Val(p.M256V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335715
Start	28592320:28592320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718T>C
AA Mutation	p.Tyr240His(p.Y240H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335715
Start	28593259:28593259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587T>C
AA Mutation	p.Met196Thr(p.M196T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335715
Start	28593488:28593488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77660804
CDS Mutation	c.453C>G
AA Mutation	p.His151Gln(p.H151Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335715
Start	28593490:28593490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760742843
CDS Mutation	c.451C>G
AA Mutation	p.His151Asp(p.H151D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335715
Start	28593496:28593496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764148152
CDS Mutation	c.445T>C
AA Mutation	p.Tyr149His(p.Y149H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335715
Start	28593548:28593548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139054845
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335715
Start	28593500:28593500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369978676
CDS Mutation	c.441A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335715
Start	28595889:28595889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187587434
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335715
Start	28595632:28595632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1126449
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000335715
Start	28592318:28592318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.720C>A
AA Mutation	p.Tyr240Ter(p.Y240*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SULT1A2

No Mutation Annotation!