Colon Cancer: Gene >> DDIAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329143
Start	82933550:82933550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2212A>G
AA Mutation	p.Ser738Gly(p.S738G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329143
Start	82933257:82933257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142322539
CDS Mutation	c.1919A>G
AA Mutation	p.Asn640Ser(p.N640S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329143
Start	82933432:82933432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2094G>T
AA Mutation	p.Gln698His(p.Q698H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329143
Start	82914801:82914801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150528544
CDS Mutation	c.63A>G
AA Mutation	p.Ile21Met(p.I21M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329143
Start	82933736:82933736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2398G>T
AA Mutation	p.Asp800Tyr(p.D800Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329143
Start	82932376:82932376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1038G>T
AA Mutation	p.Glu346Asp(p.E346D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000329143
Start	82914760:82914760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143540019
CDS Mutation	c.22C>A
AA Mutation	p.Leu8Ile(p.L8I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329143
Start	82928792:82928792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561386530
CDS Mutation	c.129A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329143
Start	82933984:82933984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2646C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329143
Start	82932943:82932943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139413374
CDS Mutation	c.1605G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329143
Start	82932934:82932934(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1601delT
AA Mutation	p.Leu534TyrfsTer16(p.L534Yfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DDIAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329143
Start	82932592:82932592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254C>A
AA Mutation	p.Phe418Leu(p.F418L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329143
Start	82932221:82932221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.883T>C
AA Mutation	p.Ser295Pro(p.S295P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000329143
Start	82932354:82932354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1016T>G
AA Mutation	p.Leu339Ter(p.L339*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript