Colon Cancer: Gene >> ERN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000433197
Start	64065216:64065216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914C>T
AA Mutation	p.Ala305Val(p.A305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000433197
Start	64047929:64047929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2458C>T
AA Mutation	p.Arg820Cys(p.R820C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000433197
Start	64047940:64047940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2447A>T
AA Mutation	p.Asp816Val(p.D816V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000433197
Start	64079676:64079676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268A>G
AA Mutation	p.Asn90Asp(p.N90D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000433197
Start	64052818:64052818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2215G>A
AA Mutation	p.Ala739Thr(p.A739T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000433197
Start	64054314:64054314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1889G>A
AA Mutation	p.Cys630Tyr(p.C630Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000433197
Start	64044083:64044083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2839G>C
AA Mutation	p.Ala947Pro(p.A947P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433197
Start	64047978:64047978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2409C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433197
Start	64052960:64052960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2073A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433197
Start	64066868:64066868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367596145
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433197
Start	64079698:64079698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433197
Start	64064047:64064047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433197
Start	64072063:64072063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374999844
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433197
Start	64043997:64043997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368375095
CDS Mutation	c.2925C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000433197
Start	64055926:64055927(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1418_1420dupAGC
AA Mutation	p.Gln473dup(p.Q473dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ERN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000433197
Start	64052800:64052800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750705699
CDS Mutation	c.2233G>A
AA Mutation	p.Glu745Lys(p.E745K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript