Colon Cancer: Gene >> ACTA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229431615:229431615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1018T>C
AA Mutation	p.Ser340Pro(p.S340P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229433091:229433091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25G>A
AA Mutation	p.Ala9Thr(p.A9T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229431891:229431891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.820G>A
AA Mutation	p.Ala274Thr(p.A274T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229433051:229433051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65G>A
AA Mutation	p.Gly22Asp(p.G22D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229432609:229432609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401T>C
AA Mutation	p.Met134Thr(p.M134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229432171:229432171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631G>A
AA Mutation	p.Val211Met(p.V211M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229432743:229432743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267C>A
AA Mutation	p.His89Gln(p.H89Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000366684
Start	229431994:229431994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>A
AA Mutation	p.Gly270Ser(p.G270S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229432874:229432874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.136A>G
AA Mutation	p.Met46Val(p.M46V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229431843:229431843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868G>A
AA Mutation	p.Asp290Asn(p.D290N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229433034:229433034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82G>A
AA Mutation	p.Ala28Thr(p.A28T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229432679:229432679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331C>A
AA Mutation	p.Pro111Thr(p.P111T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229431800:229431800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911G>A
AA Mutation	p.Gly304Asp(p.G304D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366684
Start	229432575:229432575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371410845
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366684
Start	229433068:229433068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370407621
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366684
Start	229432076:229432076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366684
Start	229432121:229432121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366684
Start	229432848:229432848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366684
Start	229431800:229431800(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.911delG
AA Mutation	p.Gly304AlafsTer24(p.G304Afs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ACTA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366684
Start	229431887:229431887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824G>A
AA Mutation	p.Gly275Asp(p.G275D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366684
Start	229432127:229432127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript