Colon Cancer: Gene >> SLC45A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367145
Start	205659382:205659382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514C>G
AA Mutation	p.Ala505Gly(p.A505G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367145
Start	205664485:205664485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172G>A
AA Mutation	p.Gly58Ser(p.G58S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367145
Start	205662088:205662088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552544292
CDS Mutation	c.997G>A
AA Mutation	p.Ala333Thr(p.A333T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367145
Start	205659335:205659335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1561A>G
AA Mutation	p.Thr521Ala(p.T521A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367145
Start	205662925:205662925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369703351
CDS Mutation	c.866C>T
AA Mutation	p.Thr289Met(p.T289M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367145
Start	205662977:205662977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370670814
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Cys(p.R272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367145
Start	205663540:205663540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762101416
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367145
Start	205663193:205663193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598T>G
AA Mutation	p.Phe200Val(p.F200V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367145
Start	205662882:205662882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753727005
CDS Mutation	c.909C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367145
Start	205659395:205659395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1501C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367145
Start	205663272:205663272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000367145
Start	205662043:205662043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Ter(p.R348*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC45A3

No Mutation Annotation!