Colon Cancer: Gene >> LTBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65547471:65547471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2075G>A
AA Mutation	p.Arg692Gln(p.R692Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65547807:65547807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1861G>A
AA Mutation	p.Glu621Lys(p.E621K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65543200:65543200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2501C>T
AA Mutation	p.Ala834Val(p.A834V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65553212:65553212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757124780
CDS Mutation	c.1015G>A
AA Mutation	p.Ala339Thr(p.A339T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65539225:65539225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3767A>T
AA Mutation	p.Asp1256Val(p.D1256V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65553469:65553469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.926C>T
AA Mutation	p.Thr309Ile(p.T309I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65552320:65552320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1273C>G
AA Mutation	p.Arg425Gly(p.R425G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65540883:65540883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2965C>T
AA Mutation	p.Pro989Ser(p.P989S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65540260:65540260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3229A>C
AA Mutation	p.Ser1077Arg(p.S1077R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65540355:65540355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752339288
CDS Mutation	c.3134A>G
AA Mutation	p.Asn1045Ser(p.N1045S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65547725:65547725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1943G>A
AA Mutation	p.Arg648His(p.R648H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65552874:65552874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752122083
CDS Mutation	c.1172G>A
AA Mutation	p.Arg391His(p.R391H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65547923:65547923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1843G>A
AA Mutation	p.Val615Met(p.V615M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301873
Start	65540875:65540875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2973C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301873
Start	65547560:65547560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1986C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301873
Start	65553515:65553515(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.880delC
AA Mutation	p.Leu294SerfsTer94(p.L294Sfs*94)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301873
Start	65547981:65547982(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1784dupC
AA Mutation	p.Asp596Ter(p.D596*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LTBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301873
Start	65551552:65551552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1544A>G
AA Mutation	p.Asp515Gly(p.D515G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript