Colon Cancer: Gene >> CYTIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264192
Start	157415843:157415843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914T>G
AA Mutation	p.Ile305Ser(p.I305S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264192
Start	157427371:157427371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526G>A
AA Mutation	p.Ala176Thr(p.A176T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264192
Start	157416075:157416075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682C>T
AA Mutation	p.Pro228Ser(p.P228S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264192
Start	157415909:157415909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848A>C
AA Mutation	p.Glu283Ala(p.E283A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264192
Start	157443952:157443952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376714958
CDS Mutation	c.69G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264192
Start	157415980:157415980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264192
Start	157415716:157415716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1041C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000264192
Start	157443855:157443855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770910230
CDS Mutation	c.166C>T
AA Mutation	p.Arg56Ter(p.R56*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000264192
Start	157418544:157418544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592C>T
AA Mutation	p.Gln198Ter(p.Q198*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CYTIP

No Mutation Annotation!