Colon Cancer: Gene >> MFHAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276282
Start	8891149:8891149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1910G>A
AA Mutation	p.Arg637His(p.R637H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276282
Start	8891882:8891882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1177G>A
AA Mutation	p.Ala393Thr(p.A393T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276282
Start	8892761:8892761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.298G>A
AA Mutation	p.Ala100Thr(p.A100T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276282
Start	8891161:8891161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1898G>A
AA Mutation	p.Arg633His(p.R633H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000276282
Start	8890319:8890319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2740T>C
AA Mutation	p.Phe914Leu(p.F914L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000276282
Start	8891470:8891470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589C>T
AA Mutation	p.Ala530Val(p.A530V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000276282
Start	8891162:8891162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1897C>T
AA Mutation	p.Arg633Cys(p.R633C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000276282
Start	8890303:8890303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780991918
CDS Mutation	c.2756A>G
AA Mutation	p.Tyr919Cys(p.Y919C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276282
Start	8890884:8890884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767806746
CDS Mutation	c.2175C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276282
Start	8892210:8892210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276282
Start	8890122:8890122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2937C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276282
Start	8892546:8892546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276282
Start	8892336:8892336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141800061
CDS Mutation	c.723G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276282
Start	8890098:8890098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2961C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MFHAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276282
Start	8891222:8891222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1837C>A
AA Mutation	p.Leu613Met(p.L613M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276282
Start	8890687:8890687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2372G>A
AA Mutation	p.Gly791Asp(p.G791D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript