Colon Cancer: Gene >> GHSR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241256
Start	172447827:172447827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587A>T
AA Mutation	p.Asn196Ile(p.N196I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241256
Start	172448386:172448386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.28C>T
AA Mutation	p.Pro10Ser(p.P10S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000241256
Start	172445298:172445298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.964C>A
AA Mutation	p.Leu322Met(p.L322M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000241256
Start	172448283:172448283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202007365
CDS Mutation	c.131C>T
AA Mutation	p.Ala44Val(p.A44V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000241256
Start	172448231:172448231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183C>G
AA Mutation	p.Asn61Lys(p.N61K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000241256
Start	172447768:172447768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.646G>A
AA Mutation	p.Val216Met(p.V216M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000241256
Start	172445291:172445291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971A>C
AA Mutation	p.Asn324Thr(p.N324T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000241256
Start	172448149:172448149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265G>A
AA Mutation	p.Asp89Asn(p.D89N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241256
Start	172448141:172448141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241256
Start	172447850:172447850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752005705
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241256
Start	172448282:172448282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000241256
Start	172447820:172447820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594C>A
AA Mutation	p.Cys198Ter(p.C198*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GHSR

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241256
Start	172448264:172448264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript