Colon Cancer: Gene >> TCTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551590
Start	110626402:110626402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.382T>C
AA Mutation	p.Ser128Pro(p.S128P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000551590
Start	110645124:110645124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1489A>T
AA Mutation	p.Arg497Trp(p.R497W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000551590
Start	110645126:110645126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1491G>T
AA Mutation	p.Arg497Ser(p.R497S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000551590
Start	110645074:110645074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1439A>C
AA Mutation	p.Gln480Pro(p.Q480P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000551590
Start	110640441:110640441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780877516
CDS Mutation	c.902G>A
AA Mutation	p.Arg301Gln(p.R301Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000551590
Start	110642308:110642308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250C>T
AA Mutation	p.Thr417Ile(p.T417I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000551590
Start	110641058:110641058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013A>G
AA Mutation	p.Glu338Gly(p.E338G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000551590
Start	110647789:110647789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373723058
CDS Mutation	c.1661C>T
AA Mutation	p.Ala554Val(p.A554V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551590
Start	110647883:110647883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370246838
CDS Mutation	c.1755G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551590
Start	110641586:110641586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759588884
CDS Mutation	c.1149C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TCTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551590
Start	110647293:110647293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773106113
CDS Mutation	c.1577T>C
AA Mutation	p.Ile526Thr(p.I526T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551590
Start	110619852:110619852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript