Colon Cancer: Gene >> IMMT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000410111
Start	86166620:86166620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680C>A
AA Mutation	p.Ala227Asp(p.A227D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000410111
Start	86146158:86146158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114088948
CDS Mutation	c.1573C>T
AA Mutation	p.Arg525Cys(p.R525C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000410111
Start	86179528:86179528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756459398
CDS Mutation	c.214C>T
AA Mutation	p.Arg72Trp(p.R72W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000410111
Start	86151430:86151430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268A>C
AA Mutation	p.Lys423Thr(p.K423T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000410111
Start	86170793:86170793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611C>T
AA Mutation	p.Ala204Val(p.A204V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000410111
Start	86162076:86162076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.796G>T
AA Mutation	p.Ala266Ser(p.A266S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000410111
Start	86179434:86179434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308C>T
AA Mutation	p.Ser103Leu(p.S103L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410111
Start	86151324:86151324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410111
Start	86171296:86171296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410111
Start	86173753:86173753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527824042
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410111
Start	86151375:86151375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000410111
Start	86146072:86146072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1659T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000410111
Start	86144597:86144597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1948G>T
AA Mutation	p.Glu650Ter(p.E650*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000410111
Start	86144390:86144390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2155C>T
AA Mutation	p.Arg719Ter(p.R719*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IMMT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000410111
Start	86179439:86179439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.303G>T
AA Mutation	p.Lys101Asn(p.K101N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000410111
Start	86146083:86146083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755867536
CDS Mutation	c.1648G>A
AA Mutation	p.Glu550Lys(p.E550K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000410111
Start	86159659:86159659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.909G>T
AA Mutation	p.Glu303Asp(p.E303D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000410111
Start	86144597:86144597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1948G>T
AA Mutation	p.Glu650Ter(p.E650*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript