Colon Cancer: Gene >> RGS6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000553530
Start	72495237:72495237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149826345
CDS Mutation	c.940G>A
AA Mutation	p.Val314Ile(p.V314I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000553530
Start	72510235:72510235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1047G>C
AA Mutation	p.Gln349His(p.Q349H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000553530
Start	72458334:72458334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299A>G
AA Mutation	p.His100Arg(p.H100R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000553530
Start	72495248:72495248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.951G>T
AA Mutation	p.Trp317Cys(p.W317C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000553530
Start	72518401:72518401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142C>T
AA Mutation	p.Ala381Val(p.A381V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000553530
Start	72472910:72472910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.575T>G
AA Mutation	p.Leu192Trp(p.L192W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000553530
Start	72465783:72465783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420G>T
AA Mutation	p.Met140Ile(p.M140I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000553530
Start	72458369:72458369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334C>T
AA Mutation	p.Arg112Cys(p.R112C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553530
Start	72518420:72518420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553530
Start	72472947:72472947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553530
Start	71964863:71964863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757753359
CDS Mutation	c.72C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553530
Start	72562446:72562446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746072430
CDS Mutation	c.1398G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000553530
Start	72518415:72518415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1156G>T
AA Mutation	p.Glu386Ter(p.E386*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000553530
Start	72474658:72474658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200924429
CDS Mutation	c.652C>T
AA Mutation	p.Arg218Ter(p.R218*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RGS6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000553530
Start	72518370:72518370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1111G>T
AA Mutation	p.Asp371Tyr(p.D371Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript