Colon Cancer: Gene >> RAD18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264926
Start	8963381:8963381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5A>T
AA Mutation	p.Asp2Val(p.D2V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264926
Start	8958921:8958921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.132C>A
AA Mutation	p.Asn44Lys(p.N44K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264926
Start	8935952:8935952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808A>C
AA Mutation	p.Asn270His(p.N270H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264926
Start	8947221:8947221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769975828
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Trp(p.R89W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264926
Start	8902422:8902422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1126A>G
AA Mutation	p.Lys376Glu(p.K376E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264926
Start	8881415:8881415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149913355
CDS Mutation	c.1430G>A
AA Mutation	p.Arg477His(p.R477H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264926
Start	8941667:8941667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404A>C
AA Mutation	p.Asn135Thr(p.N135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264926
Start	8939579:8939579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781347031
CDS Mutation	c.679G>A
AA Mutation	p.Glu227Lys(p.E227K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264926
Start	8941536:8941536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767423682
CDS Mutation	c.535G>A
AA Mutation	p.Ala179Thr(p.A179T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000264926
Start	8935922:8935922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838G>T
AA Mutation	p.Glu280Ter(p.E280*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264926
Start	8902436:8902437(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs766463274
CDS Mutation	c.1111dupA
AA Mutation	p.Thr371AsnfsTer9(p.T371Nfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000264926
Start	8941759:8941761(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs766404991
CDS Mutation	c.310_312delCCT
AA Mutation	p.Pro104del(p.P104del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000264926
Start	8939576:8939577(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.681_682insCAG
AA Mutation	p.Glu227_Glu228insGln(p.E227_E228insQ)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RAD18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264926
Start	8947265:8947265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221A>C
AA Mutation	p.Asn74Thr(p.N74T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264926
Start	8941741:8941741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330G>T
AA Mutation	p.Lys110Asn(p.K110N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript