Colon Cancer: Gene >> DACT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366795
Start	168310249:168310249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745550369
CDS Mutation	c.577G>A
AA Mutation	p.Glu193Lys(p.E193K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366795
Start	168308855:168308855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902C>A
AA Mutation	p.Pro301His(p.P301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366795
Start	168308232:168308232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1525A>G
AA Mutation	p.Arg509Gly(p.R509G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366795
Start	168308353:168308353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1404C>A
AA Mutation	p.Asp468Glu(p.D468E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366795
Start	168310217:168310217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609G>T
AA Mutation	p.Glu203Asp(p.E203D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366795
Start	168308121:168308121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1636C>T
AA Mutation	p.Leu546Phe(p.L546F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366795
Start	168308742:168308742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015C>T
AA Mutation	p.His339Tyr(p.H339Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000366795
Start	168310426:168310426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369801873
CDS Mutation	c.400G>A
AA Mutation	p.Gly134Ser(p.G134S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366795
Start	168307639:168307639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2118C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366795
Start	168307675:168307675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377529965
CDS Mutation	c.2082C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366795
Start	168307711:168307711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571812546
CDS Mutation	c.2046C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366795
Start	168308635:168308635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1122C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366795
Start	168310241:168310241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366795
Start	168308920:168308920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366795
Start	168308895:168308895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.862C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366795
Start	168308172:168308172(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1585delC
AA Mutation	p.Gln529SerfsTer228(p.Q529Sfs*228)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DACT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366795
Start	168308124:168308124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775639779
CDS Mutation	c.1633G>A
AA Mutation	p.Gly545Arg(p.G545R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366795
Start	168307475:168307475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781247710
CDS Mutation	c.2282G>A
AA Mutation	p.Arg761His(p.R761H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366795
Start	168310430:168310430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366795
Start	168310202:168310202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773399129
CDS Mutation	c.624G>A
Mutation Classification	Silent
Feature Type	Transcript