Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SHISA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319234
Start	42401393:42401393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659C>A
AA Mutation	p.Pro220His(p.P220H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319234
Start	42401261:42401261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.527G>A
AA Mutation	p.Arg176His(p.R176H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319234
Start	42401388:42401388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319234
Start	42398158:42398158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771746182
CDS Mutation	c.102G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319234
Start	42398233:42398233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319234
Start	42398113:42398113(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.59delG
AA Mutation	p.Gly20AlafsTer96(p.G20Afs*96)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SHISA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319234
Start	42401150:42401150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
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	ENST00000319234
Start	42398100:42398100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755434589
CDS Mutation	c.44G>A
AA Mutation	p.Arg15His(p.R15H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319234
Start	42401124:42401124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript