Colon Cancer: Gene >> SLC28A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347644
Start	45265629:45265629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.827A>G
AA Mutation	p.Tyr276Cys(p.Y276C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347644
Start	45265603:45265603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801C>A
AA Mutation	p.Phe267Leu(p.F267L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347644
Start	45272312:45272312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536193391
CDS Mutation	c.1666C>T
AA Mutation	p.Arg556Trp(p.R556W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000347644
Start	45266114:45266114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895A>T
AA Mutation	p.Thr299Ser(p.T299S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000347644
Start	45268378:45268378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1368G>T
AA Mutation	p.Gln456His(p.Q456H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000347644
Start	45272673:45272673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1748G>A
AA Mutation	p.Gly583Glu(p.G583E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000347644
Start	45275427:45275427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1891T>G
AA Mutation	p.Phe631Val(p.F631V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000347644
Start	45267477:45267477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766781227
CDS Mutation	c.965G>A
AA Mutation	p.Arg322His(p.R322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347644
Start	45264723:45264723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347644
Start	45253488:45253488(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.142delG
AA Mutation	p.Asp48MetfsTer52(p.D48Mfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000347644
Start	45267665:45267665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC28A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347644
Start	45268248:45268248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238C>T
AA Mutation	p.Ala413Val(p.A413V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347644
Start	45265154:45265154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768C>A
Mutation Classification	Silent
Feature Type	Transcript