Colon Cancer: Gene >> FLYWCH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253928
Start	2933206:2933206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873G>T
AA Mutation	p.Lys291Asn(p.K291N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253928
Start	2933573:2933573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529892902
CDS Mutation	c.1240G>A
AA Mutation	p.Ala414Thr(p.A414T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253928
Start	2933505:2933505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202152304
CDS Mutation	c.1172G>A
AA Mutation	p.Arg391Gln(p.R391Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253928
Start	2938277:2938277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1871G>T
AA Mutation	p.Gly624Val(p.G624V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253928
Start	2937295:2937295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780119016
CDS Mutation	c.1688G>A
AA Mutation	p.Arg563His(p.R563H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000253928
Start	2933276:2933276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377699630
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Trp(p.R315W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000253928
Start	2930419:2930419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335A>G
AA Mutation	p.Gln112Arg(p.Q112R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253928
Start	2933572:2933572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749707471
CDS Mutation	c.1239C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253928
Start	2929913:2929913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183328490
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253928
Start	2933437:2933437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774388764
CDS Mutation	c.1104C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253928
Start	2937125:2937125(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1521delC
AA Mutation	p.Glu508SerfsTer3(p.E508Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000253928
Start	2933364:2933366(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs767735750
CDS Mutation	c.1033_1035delGAG
AA Mutation	p.Glu345del(p.E345del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FLYWCH1

No Mutation Annotation!