Colon Cancer: Gene >> AVPR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337474
Start	153906601:153906601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989G>A
AA Mutation	p.Ser330Asn(p.S330N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337474
Start	153906203:153906203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697C>A
AA Mutation	p.His233Asn(p.H233N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337474
Start	153906261:153906261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368306347
CDS Mutation	c.755G>A
AA Mutation	p.Arg252Gln(p.R252Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337474
Start	153906625:153906625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1013G>A
AA Mutation	p.Ser338Asn(p.S338N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000337474
Start	153906573:153906573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961A>G
AA Mutation	p.Asn321Asp(p.N321D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000337474
Start	153906111:153906111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781891175
CDS Mutation	c.605G>A
AA Mutation	p.Arg202His(p.R202H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000337474
Start	153906096:153906096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590C>T
AA Mutation	p.Ala197Val(p.A197V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337474
Start	153906097:153906097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781939531
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337474
Start	153906091:153906091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AVPR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337474
Start	153906675:153906675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063G>T
AA Mutation	p.Asp355Tyr(p.D355Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript