Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> XCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309285
Start	46021532:46021532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199898916
CDS Mutation	c.416G>A
AA Mutation	p.Arg139His(p.R139H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309285
Start	46021193:46021193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745583108
CDS Mutation	c.755G>A
AA Mutation	p.Arg252Gln(p.R252Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309285
Start	46021851:46021851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97G>T
AA Mutation	p.Ala33Ser(p.A33S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309285
Start	46021280:46021280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668C>T
AA Mutation	p.Thr223Met(p.T223M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309285
Start	46021531:46021531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752197806
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309285
Start	46021908:46021908(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.40delT
AA Mutation	p.Tyr14ThrfsTer33(p.Y14Tfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> XCR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309285
Start	46021413:46021413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754430378
CDS Mutation	c.535G>A
AA Mutation	p.Glu179Lys(p.E179K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309285
Start	46021529:46021529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419T>C
AA Mutation	p.Val140Ala(p.V140A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309285
Start	46021170:46021170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755102288
CDS Mutation	c.778G>A
AA Mutation	p.Glu260Lys(p.E260K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309285
Start	46021414:46021414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148266059
CDS Mutation	c.534C>T
Mutation Classification	Silent
Feature Type	Transcript