Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC16A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112917841:112917841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565T>G
AA Mutation	p.Cys189Gly(p.C189G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112917423:112917423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774823539
CDS Mutation	c.983G>A
AA Mutation	p.Arg328Gln(p.R328Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112917898:112917898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508G>T
AA Mutation	p.Gly170Cys(p.G170C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112913943:112913943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767509828
CDS Mutation	c.1451C>T
AA Mutation	p.Pro484Leu(p.P484L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112917876:112917876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530G>T
AA Mutation	p.Ser177Ile(p.S177I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112922103:112922103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248A>G
AA Mutation	p.Tyr83Cys(p.Y83C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112929187:112929187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.122C>A
AA Mutation	p.Thr41Asn(p.T41N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112917405:112917405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763573918
CDS Mutation	c.1001C>T
AA Mutation	p.Ala334Val(p.A334V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112917912:112917912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.494A>G
AA Mutation	p.Asn165Ser(p.N165S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369626
Start	112914110:112914110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774103196
CDS Mutation	c.1284C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369626
Start	112929276:112929276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369626
Start	112917581:112917581(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs150151185
CDS Mutation	c.825delT
AA Mutation	p.Phe275LeufsTer37(p.F275Lfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369626
Start	112929268:112929268(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.41delC
AA Mutation	p.Pro14GlnfsTer10(p.P14Qfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC16A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112917882:112917882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524G>A
AA Mutation	p.Arg175Lys(p.R175K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369626
Start	112917423:112917423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774823539
CDS Mutation	c.983G>A
AA Mutation	p.Arg328Gln(p.R328Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369626
Start	112917812:112917812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755634416
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369626
Start	112914110:112914110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774103196
CDS Mutation	c.1284C>T
Mutation Classification	Silent
Feature Type	Transcript