Colon Cancer: Gene >> ELAVL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351593
Start	7963802:7963802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662C>T
AA Mutation	p.Ser221Phe(p.S221F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000351593
Start	7973728:7973728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427A>G
AA Mutation	p.Thr143Ala(p.T143A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000351593
Start	7963747:7963747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717C>G
AA Mutation	p.Asn239Lys(p.N239K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000351593
Start	7981129:7981129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230C>T
AA Mutation	p.Ala77Val(p.A77V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000351593
Start	7991757:7991757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59C>T
AA Mutation	p.Thr20Met(p.T20M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000351593
Start	7963590:7963590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874A>G
AA Mutation	p.Met292Val(p.M292V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351593
Start	7967600:7967600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377051094
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351593
Start	7967645:7967645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772532543
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351593
Start	7967639:7967639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.582A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351593
Start	7963765:7963765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200745899
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000351593
Start	7981129:7981130(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.228_229dupAG
AA Mutation	p.Ala77GlufsTer6(p.A77Efs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ELAVL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351593
Start	7981156:7981156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203A>G
AA Mutation	p.Tyr68Cys(p.Y68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351593
Start	7963507:7963507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000351593
Start	7991789:7991790(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.26_27delTG
AA Mutation	p.Met9SerfsTer7(p.M9Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript