Colon Cancer: Gene >> FADS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278840
Start	61848234:61848234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694G>A
AA Mutation	p.Asp232Asn(p.D232N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278840
Start	61828512:61828512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122G>A
AA Mutation	p.Arg41His(p.R41H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278840
Start	61857460:61857460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812C>T
AA Mutation	p.Pro271Leu(p.P271L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278840
Start	61865172:61865172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178G>A
AA Mutation	p.Arg393Gln(p.R393Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278840
Start	61840431:61840431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.416A>T
AA Mutation	p.His139Leu(p.H139L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000278840
Start	61840443:61840443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.428T>C
AA Mutation	p.Leu143Pro(p.L143P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000278840
Start	61828539:61828539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149C>T
AA Mutation	p.Ser50Phe(p.S50F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000278840
Start	61840691:61840691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584A>T
AA Mutation	p.His195Leu(p.H195L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278840
Start	61837813:61837813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377238578
CDS Mutation	c.243C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278840
Start	61837789:61837789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545952540
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	start_lost
Transcription ID	ENST00000278840
Start	61828392:61828392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FADS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278840
Start	61865196:61865196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202C>T
AA Mutation	p.Pro401Leu(p.P401L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278840
Start	61840356:61840356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778333968
CDS Mutation	c.341G>A
AA Mutation	p.Arg114Gln(p.R114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript