Colon Cancer: Gene >> BCAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75229829:75229829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2295C>A
AA Mutation	p.Phe765Leu(p.F765L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75229759:75229759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2365G>A
AA Mutation	p.Ala789Thr(p.A789T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75235356:75235356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746131932
CDS Mutation	c.1543G>A
AA Mutation	p.Val515Ile(p.V515I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75237328:75237328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747374409
CDS Mutation	c.650G>A
AA Mutation	p.Arg217His(p.R217H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75237215:75237215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558331437
CDS Mutation	c.763C>T
AA Mutation	p.Arg255Trp(p.R255W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75242601:75242601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502C>T
AA Mutation	p.Pro168Ser(p.P168S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75236904:75236904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.890T>G
AA Mutation	p.Leu297Arg(p.L297R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75242927:75242927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176G>A
AA Mutation	p.Arg59His(p.R59H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75235623:75235623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779814700
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Cys(p.R426C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75235113:75235113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1786T>C
AA Mutation	p.Phe596Leu(p.F596L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000162330
Start	75235097:75235097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1802C>A
AA Mutation	p.Ala601Asp(p.A601D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000162330
Start	75229697:75229697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2427C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000162330
Start	75236957:75236957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000162330
Start	75235030:75235030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1869C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000162330
Start	75235738:75235738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553690024
CDS Mutation	c.1161C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BCAR1

No Mutation Annotation!