Colon Cancer: Gene >> ZNF219

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360947
Start	21092361:21092361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.936G>T
AA Mutation	p.Lys312Asn(p.K312N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360947
Start	21092404:21092404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893C>G
AA Mutation	p.Ala298Gly(p.A298G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360947
Start	21090765:21090765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940G>A
AA Mutation	p.Arg647His(p.R647H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360947
Start	21090897:21090897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560844867
CDS Mutation	c.1808C>T
AA Mutation	p.Pro603Leu(p.P603L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360947
Start	21090676:21090676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2029C>T
AA Mutation	p.Arg677Trp(p.R677W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360947
Start	21092118:21092118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360947
Start	21091929:21091929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1368G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360947
Start	21093189:21093189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360947
Start	21090749:21090749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772027830
CDS Mutation	c.1956G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360947
Start	21093036:21093036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360947
Start	21090548:21090548(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2157delG
AA Mutation	p.Gln720LysfsTer28(p.Q720Kfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF219

No Mutation Annotation!