Colon Cancer: Gene >> TCF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55279555:55279555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651G>A
AA Mutation	p.Met217Ile(p.M217I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55229033:55229033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1681C>T
AA Mutation	p.Arg561Cys(p.R561C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55254646:55254646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1201C>T
AA Mutation	p.Arg401Trp(p.R401W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55254649:55254649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198C>A
AA Mutation	p.Leu400Ile(p.L400I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398339
Start	55635747:55635747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.151T>C
AA Mutation	p.Trp51Arg(p.W51R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55254571:55254571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1276C>T
AA Mutation	p.His426Tyr(p.H426Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55587056:55587056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61G>T
AA Mutation	p.Asp21Tyr(p.D21Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55232606:55232606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1552G>A
AA Mutation	p.Glu518Lys(p.E518K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55228877:55228877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1837G>A
AA Mutation	p.Val613Ile(p.V613I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55350980:55350980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.393G>A
AA Mutation	p.Met131Ile(p.M131I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55260020:55260020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998C>A
AA Mutation	p.Ser333Tyr(p.S333Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356073
Start	55585311:55585311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356073
Start	55585311:55585311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.114T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356073
Start	55228953:55228953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761419131
CDS Mutation	c.1761C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356073
Start	55228289:55228289(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1940delC
AA Mutation	p.Pro647LeufsTer32(p.P647Lfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000356073
Start	55350388:55350388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Ter(p.R174*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TCF4

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356073
Start	55587046:55587046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.71C>T
AA Mutation	p.Ala24Val(p.A24V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55269923:55269923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830T>G
AA Mutation	p.Leu277Arg(p.L277R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356073
Start	55261467:55261467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989C>T
AA Mutation	p.Ser330Leu(p.S330L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55254693:55254693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154G>A
AA Mutation	p.Arg385Gln(p.R385Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356073
Start	55228247:55228247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1982C>T
AA Mutation	p.Ser661Leu(p.S661L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356073
Start	55228953:55228953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761419131
CDS Mutation	c.1761C>T
Mutation Classification	Silent
Feature Type	Transcript