Colon Cancer: Gene >> VIT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36755013:36755013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368C>T
AA Mutation	p.Ser123Leu(p.S123L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36805469:36805469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149C>A
AA Mutation	p.Phe383Leu(p.F383L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36814254:36814254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750426305
CDS Mutation	c.1930G>A
AA Mutation	p.Ala644Thr(p.A644T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36805595:36805595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1275C>A
AA Mutation	p.Phe425Leu(p.F425L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36808743:36808743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1616A>G
AA Mutation	p.Tyr539Cys(p.Y539C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36808831:36808831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1704G>T
AA Mutation	p.Trp568Cys(p.W568C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36773806:36773806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.695C>T
AA Mutation	p.Ala232Val(p.A232V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36759030:36759030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.471T>G
AA Mutation	p.Ser157Arg(p.S157R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36787182:36787182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748465900
CDS Mutation	c.919C>T
AA Mutation	p.Arg307Trp(p.R307W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389975
Start	36755002:36755002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389975
Start	36814205:36814205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751166847
CDS Mutation	c.1881C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389975
Start	36808849:36808849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34147001
CDS Mutation	c.1722G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389975
Start	36743119:36743119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373107899
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000389975
Start	36783354:36783354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.817G>T
AA Mutation	p.Glu273Ter(p.E273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000389975
Start	36759017:36759017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.458C>A
AA Mutation	p.Ser153Ter(p.S153*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> VIT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36787248:36787248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146415075
CDS Mutation	c.985G>A
AA Mutation	p.Gly329Ser(p.G329S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36743243:36743243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202044807
CDS Mutation	c.262G>A
AA Mutation	p.Ala88Thr(p.A88T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36814198:36814198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141772569
CDS Mutation	c.1874C>T
AA Mutation	p.Ala625Val(p.A625V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36814260:36814260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1936G>T
AA Mutation	p.Asp646Tyr(p.D646Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36754958:36754958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751810783
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Trp(p.R105W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36767129:36767129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523C>A
AA Mutation	p.Pro175Thr(p.P175T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389975
Start	36767232:36767232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626C>A
AA Mutation	p.Ser209Tyr(p.S209Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript