Colon Cancer: Gene >> GNB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000232564
Start	179405364:179405364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742G>A
AA Mutation	p.Ala248Thr(p.A248T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000232564
Start	179401216:179401216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1020T>A
AA Mutation	p.Asn340Lys(p.N340K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000232564
Start	179405336:179405336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770C>T
AA Mutation	p.Ala257Val(p.A257V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000232564
Start	179419406:179419406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.196G>A
AA Mutation	p.Asp66Asn(p.D66N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000232564
Start	179413597:179413597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755864696
CDS Mutation	c.514G>A
AA Mutation	p.Glu172Lys(p.E172K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000232564
Start	179419436:179419436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.166G>A
AA Mutation	p.Ala56Thr(p.A56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000232564
Start	179426194:179426194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7G>A
AA Mutation	p.Glu3Lys(p.E3K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000232564
Start	179419465:179419465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755914601
CDS Mutation	c.137G>A
AA Mutation	p.Arg46Gln(p.R46Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000232564
Start	179414963:179414963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352G>A
AA Mutation	p.Asp118Asn(p.D118N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000232564
Start	179405219:179405219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887T>C
AA Mutation	p.Val296Ala(p.V296A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232564
Start	179413442:179413442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751438259
CDS Mutation	c.669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232564
Start	179413598:179413598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367709368
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000232564
Start	179416524:179416524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236T>G
AA Mutation	p.Leu79Ter(p.L79*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000232564
Start	179414906:179414906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767993499
CDS Mutation	c.409C>T
AA Mutation	p.Arg137Ter(p.R137*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant;start_lost
Transcription ID	ENST00000232564
Start	179426199:179426200(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1dupA
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GNB4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232564
Start	179416525:179416525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235T>C
Mutation Classification	Silent
Feature Type	Transcript