Colon Cancer: Gene >> SDAD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356260
Start	75956056:75956056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1935G>T
AA Mutation	p.Lys645Asn(p.K645N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356260
Start	75956063:75956063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1928A>C
AA Mutation	p.Lys643Thr(p.K643T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356260
Start	75956010:75956010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202126090
CDS Mutation	c.1981C>T
AA Mutation	p.Arg661Trp(p.R661W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356260
Start	75977749:75977749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302G>A
AA Mutation	p.Cys101Tyr(p.C101Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356260
Start	75961048:75961048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336A>G
AA Mutation	p.Met446Val(p.M446V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356260
Start	75950787:75950787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145814675
CDS Mutation	c.2027G>A
AA Mutation	p.Arg676Gln(p.R676Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356260
Start	75975963:75975963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438G>T
AA Mutation	p.Lys146Asn(p.K146N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356260
Start	75960070:75960070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1479T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356260
Start	75970334:75970334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356260
Start	75970368:75970368(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.824delA
AA Mutation	p.Lys275ArgfsTer15(p.K275Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000356260
Start	75957588:75957588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1699G>T
AA Mutation	p.Glu567Ter(p.E567*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SDAD1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356260
Start	75956071:75956071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746008352
CDS Mutation	c.1920G>A
Mutation Classification	Silent
Feature Type	Transcript