Colon Cancer: Gene >> LATS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20981486:20981486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2645C>T
AA Mutation	p.Pro882Leu(p.P882L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20991364:20991364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383G>T
AA Mutation	p.Ser128Ile(p.S128I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20983388:20983388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2318C>T
AA Mutation	p.Ala773Val(p.A773V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20983398:20983398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2308T>C
AA Mutation	p.Phe770Leu(p.F770L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20975144:20975144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2993A>G
AA Mutation	p.Asp998Gly(p.D998G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20989029:20989029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766080720
CDS Mutation	c.751G>A
AA Mutation	p.Ala251Thr(p.A251T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20983586:20983586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2120G>A
AA Mutation	p.Arg707Gln(p.R707Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20975203:20975203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2934C>A
AA Mutation	p.Phe978Leu(p.F978L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	21045980:21045980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>A
AA Mutation	p.Arg16Gln(p.R16Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20988042:20988042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1738G>A
AA Mutation	p.Val580Ile(p.V580I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20988725:20988725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055G>A
AA Mutation	p.Arg352Gln(p.R352Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20989206:20989206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574G>A
AA Mutation	p.Glu192Lys(p.E192K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20983683:20983683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2023G>T
AA Mutation	p.Gly675Trp(p.G675W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20975092:20975092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762984472
CDS Mutation	c.3045C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20983633:20983633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775335330
CDS Mutation	c.2073C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20988262:20988262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751957428
CDS Mutation	c.1518C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20989078:20989078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	21045772:21045772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20979751:20979751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2712C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382592
Start	20983678:20983678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2028C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LATS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20979750:20979750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2713G>A
AA Mutation	p.Glu905Lys(p.E905K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	20988099:20988099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1681G>A
AA Mutation	p.Ala561Thr(p.A561T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	21045929:21045929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139154828
CDS Mutation	c.98C>T
AA Mutation	p.Ser33Leu(p.S33L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382592
Start	21045962:21045962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65T>G
AA Mutation	p.Ile22Ser(p.I22S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript