Colon Cancer: Gene >> ZNF358

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394341
Start	7519441:7519441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Val67Ile(p.V67I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394341
Start	7520477:7520477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1235C>T
AA Mutation	p.Ala412Val(p.A412V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394341
Start	7519330:7519330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88G>T
AA Mutation	p.Asp30Tyr(p.D30Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394341
Start	7520428:7520428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1186G>C
AA Mutation	p.Val396Leu(p.V396L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394341
Start	7520123:7520123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757547243
CDS Mutation	c.881C>T
AA Mutation	p.Pro294Leu(p.P294L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394341
Start	7520445:7520445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394341
Start	7519347:7519347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761138466
CDS Mutation	c.105T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF358

No Mutation Annotation!