Colon Cancer: Gene >> AMHR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257863
Start	53424413:53424413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757117832
CDS Mutation	c.175C>T
AA Mutation	p.Arg59Cys(p.R59C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257863
Start	53424821:53424821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345C>A
AA Mutation	p.Phe115Leu(p.F115L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000257863
Start	53425242:53425242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374601719
CDS Mutation	c.502G>A
AA Mutation	p.Ala168Thr(p.A168T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257863
Start	53425860:53425860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369599312
CDS Mutation	c.793C>T
AA Mutation	p.Arg265Trp(p.R265W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257863
Start	53425800:53425800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733G>A
AA Mutation	p.Ala245Thr(p.A245T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257863
Start	53429480:53429480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746307025
CDS Mutation	c.995G>A
AA Mutation	p.Arg332Gln(p.R332Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257863
Start	53431303:53431303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1552C>A
AA Mutation	p.Pro518Thr(p.P518T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000257863
Start	53430245:53430245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765635891
CDS Mutation	c.1388G>A
AA Mutation	p.Arg463His(p.R463H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257863
Start	53424785:53424785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753698788
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257863
Start	53429956:53429956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AMHR2

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257863
Start	53425860:53425861(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs748387033
CDS Mutation	c.800dupG
AA Mutation	p.Pro268SerfsTer30(p.P268Sfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript