Colon Cancer: Gene >> GNAO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262493
Start	56351414:56351414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754G>A
AA Mutation	p.Asp252Asn(p.D252N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262493
Start	56336816:56336816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679G>A
AA Mutation	p.Ala227Thr(p.A227T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262493
Start	56328761:56328761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434G>A
AA Mutation	p.Arg145Gln(p.R145Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262493
Start	56351405:56351405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745A>G
AA Mutation	p.Met249Val(p.M249V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262493
Start	56355033:56355033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045C>T
AA Mutation	p.Arg349Trp(p.R349W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262493
Start	56328716:56328716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200127285
CDS Mutation	c.389G>A
AA Mutation	p.Arg130Gln(p.R130Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262493
Start	56351417:56351417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757T>G
AA Mutation	p.Ser253Ala(p.S253A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262493
Start	56328707:56328707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380C>A
AA Mutation	p.Ala127Asp(p.A127D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262493
Start	56355042:56355042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054G>A
AA Mutation	p.Gly352Ser(p.G352S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262493
Start	56275978:56275978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.209A>C
AA Mutation	p.Lys70Thr(p.K70T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262493
Start	56328771:56328771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262493
Start	56354885:56354885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148878451
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262493
Start	56275964:56275964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368113345
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262493
Start	56328738:56328738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262493
Start	56334759:56334759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745503611
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262493
Start	56355041:56355041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000262493
Start	56192253:56192254(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.21_32dupAGAGGAGAGAGC
AA Mutation	p.Glu8_Ala11dup(p.E8_A11dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GNAO1

No Mutation Annotation!