Colon Cancer: Gene >> SPRY4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000434127
Start	142314874:142314874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755750768
CDS Mutation	c.235G>A
AA Mutation	p.Ala79Thr(p.A79T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000434127
Start	142314412:142314412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761651255
CDS Mutation	c.697G>A
AA Mutation	p.Ala233Thr(p.A233T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000434127
Start	142314295:142314295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531177415
CDS Mutation	c.814G>A
AA Mutation	p.Gly272Ser(p.G272S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434127
Start	142314377:142314377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.732G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434127
Start	142314452:142314452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542372364
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434127
Start	142314413:142314413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375722281
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434127
Start	142314367:142314367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434127
Start	142314851:142314851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434127
Start	142314470:142314470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.639G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000434127
Start	142314894:142314894(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.215delC
AA Mutation	p.Pro72GlnfsTer28(p.P72Qfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000434127
Start	142314589:142314589(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.520delC
AA Mutation	p.Arg174GlyfsTer85(p.R174Gfs*85)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SPRY4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434127
Start	142314275:142314275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530411114
CDS Mutation	c.834G>A
Mutation Classification	Silent
Feature Type	Transcript