Colon Cancer: Gene >> ARSB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78780564:78780564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758641798
CDS Mutation	c.1435C>T
AA Mutation	p.Arg479Trp(p.R479W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78964588:78964588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518A>G
AA Mutation	p.Glu173Gly(p.E173G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78885806:78885806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920C>A
AA Mutation	p.Ala307Glu(p.A307E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78955493:78955493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700C>A
AA Mutation	p.Leu234Ile(p.L234I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78964567:78964567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139788949
CDS Mutation	c.539G>A
AA Mutation	p.Arg180His(p.R180H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78964603:78964603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503A>G
AA Mutation	p.Tyr168Cys(p.Y168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78955333:78955333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860G>A
AA Mutation	p.Ser287Asn(p.S287N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78780516:78780516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138643812
CDS Mutation	c.1483G>A
AA Mutation	p.Val495Ile(p.V495I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78780498:78780498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1501C>T
AA Mutation	p.Arg501Cys(p.R501C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78885750:78885750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529444755
CDS Mutation	c.976G>A
AA Mutation	p.Val326Ile(p.V326I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264914
Start	78885636:78885636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090C>T
AA Mutation	p.His364Tyr(p.H364Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264914
Start	78839381:78839381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264914
Start	78964494:78964494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264914
Start	78885619:78885619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ARSB

No Mutation Annotation!