Colon Cancer: Gene >> MTNR1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92981779:92981779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745342258
CDS Mutation	c.556C>T
AA Mutation	p.Arg186Cys(p.R186C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92982131:92982131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.908T>C
AA Mutation	p.Leu303Pro(p.L303P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92982212:92982212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145300624
CDS Mutation	c.989G>A
AA Mutation	p.Arg330Gln(p.R330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92981809:92981809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777474311
CDS Mutation	c.586G>A
AA Mutation	p.Ala196Thr(p.A196T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92981827:92981827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604G>A
AA Mutation	p.Ala202Thr(p.A202T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92981566:92981566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343G>A
AA Mutation	p.Ala115Thr(p.A115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92981672:92981672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777351825
CDS Mutation	c.449G>A
AA Mutation	p.Arg150Gln(p.R150Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92981677:92981677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454T>C
AA Mutation	p.Tyr152His(p.Y152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92982190:92982190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967C>A
AA Mutation	p.Leu323Ile(p.L323I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257068
Start	92981535:92981535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139515067
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257068
Start	92982102:92982102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000257068
Start	92982061:92982061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838G>T
AA Mutation	p.Glu280Ter(p.E280*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MTNR1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92981593:92981593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145440211
CDS Mutation	c.370G>A
AA Mutation	p.Val124Ile(p.V124I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92982010:92982010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.787T>A
AA Mutation	p.Cys263Ser(p.C263S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92969882:92969882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.157G>A
AA Mutation	p.Val53Met(p.V53M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92981887:92981887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549634756
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Cys(p.R222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257068
Start	92981518:92981518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150570442
CDS Mutation	c.295G>A
AA Mutation	p.Val99Met(p.V99M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257068
Start	92982054:92982054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript