Colon Cancer: Gene >> WNT5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55470307:55470307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928G>A
AA Mutation	p.Val310Met(p.V310M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55479399:55479399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306A>C
AA Mutation	p.Lys102Asn(p.K102N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55470477:55470477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758G>T
AA Mutation	p.Trp253Leu(p.W253L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55474471:55474471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550G>A
AA Mutation	p.Asp184Asn(p.D184N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55474579:55474579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.442A>T
AA Mutation	p.Asn148Tyr(p.N148Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55470394:55470394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533153165
CDS Mutation	c.841C>T
AA Mutation	p.Arg281Trp(p.R281W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55474341:55474341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680G>A
AA Mutation	p.Arg227His(p.R227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55470214:55470214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1021G>T
AA Mutation	p.Gly341Cys(p.G341C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55470276:55470276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.959C>T
AA Mutation	p.Thr320Met(p.T320M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55474426:55474426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181787192
CDS Mutation	c.595G>A
AA Mutation	p.Ala199Thr(p.A199T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55470279:55470279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956G>A
AA Mutation	p.Gly319Asp(p.G319D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264634
Start	55479562:55479562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369165725
CDS Mutation	c.143C>T
AA Mutation	p.Ser48Leu(p.S48L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55470252:55470252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201975128
CDS Mutation	c.983C>T
AA Mutation	p.Thr328Met(p.T328M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000264634
Start	55480797:55480797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128C>T
AA Mutation	p.Ala43Val(p.A43V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264634
Start	55470275:55470275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.960G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264634
Start	55479561:55479561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264634
Start	55470122:55470122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751084010
CDS Mutation	c.1113G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264634
Start	55474421:55474421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756967642
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264634
Start	55470308:55470308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264634
Start	55480920:55480920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> WNT5A

No Mutation Annotation!