Colon Cancer: Gene >> VAC14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261776
Start	70786259:70786259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211G>A
AA Mutation	p.Gly71Arg(p.G71R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261776
Start	70800860:70800860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41T>A
AA Mutation	p.Ile14Asn(p.I14N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261776
Start	70698765:70698765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1708G>T
AA Mutation	p.Ala570Ser(p.A570S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261776
Start	70731505:70731505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1651T>G
AA Mutation	p.Phe551Val(p.F551V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261776
Start	70762569:70762569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1342C>A
AA Mutation	p.Leu448Met(p.L448M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261776
Start	70785806:70785806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.319A>T
AA Mutation	p.Ser107Cys(p.S107C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261776
Start	70783538:70783538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611C>T
AA Mutation	p.Ser204Leu(p.S204L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261776
Start	70698742:70698742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731G>T
AA Mutation	p.Glu577Asp(p.E577D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261776
Start	70762591:70762591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78503253
CDS Mutation	c.1320G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261776
Start	70781885:70781885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145425796
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261776
Start	70692957:70692957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261776
Start	70784809:70784809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261776
Start	70780862:70780862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1024C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VAC14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261776
Start	70698750:70698750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145938865
CDS Mutation	c.1723C>T
AA Mutation	p.Arg575Trp(p.R575W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261776
Start	70731606:70731606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550C>A
AA Mutation	p.Ser517Tyr(p.S517Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript