Colon Cancer: Gene >> FPGS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373247
Start	127808247:127808247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758C>G
AA Mutation	p.Ala253Gly(p.A253G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373247
Start	127813393:127813393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1553G>A
AA Mutation	p.Ser518Asn(p.S518N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373247
Start	127810068:127810068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249G>A
AA Mutation	p.Gly417Arg(p.G417R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373247
Start	127813323:127813323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483G>A
AA Mutation	p.Gly495Ser(p.G495S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373247
Start	127810967:127810967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1310T>C
AA Mutation	p.Val437Ala(p.V437A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373247
Start	127804542:127804542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311C>T
AA Mutation	p.Thr104Met(p.T104M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373247
Start	127808617:127808617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373247
Start	127808593:127808593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149509788
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373247
Start	127804531:127804531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143843163
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373247
Start	127808611:127808611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780261977
CDS Mutation	c.876G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FPGS

No Mutation Annotation!