Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CALB2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302628
Start	71384025:71384025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.533G>T
AA Mutation	p.Arg178Leu(p.R178L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302628
Start	71377688:71377688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748994795
CDS Mutation	c.283G>A
AA Mutation	p.Glu95Lys(p.E95K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302628
Start	71382744:71382744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368G>T
AA Mutation	p.Arg123Met(p.R123M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302628
Start	71382744:71382744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368G>A
AA Mutation	p.Arg123Lys(p.R123K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302628
Start	71384363:71384363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302628
Start	71377726:71377726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302628
Start	71389854:71389854(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.810delC
AA Mutation	p.Met271CysfsTer60(p.M271Cfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CALB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302628
Start	71377688:71377688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748994795
CDS Mutation	c.283G>A
AA Mutation	p.Glu95Lys(p.E95K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302628
Start	71383405:71383405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760026354
CDS Mutation	c.438G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302628
Start	71385633:71385633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139080757
CDS Mutation	c.684C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302628
Start	71383396:71383396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript