Colon Cancer: Gene >> ZFP36L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336440
Start	68790069:68790069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481T>G
AA Mutation	p.Phe161Val(p.F161V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336440
Start	68790290:68790290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260G>A
AA Mutation	p.Arg87Gln(p.R87Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336440
Start	68789708:68789708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842C>T
AA Mutation	p.Pro281Leu(p.P281L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336440
Start	68790042:68790042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508G>T
AA Mutation	p.Gly170Trp(p.G170W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336440
Start	68790186:68790186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364C>T
AA Mutation	p.Pro122Ser(p.P122S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336440
Start	68789687:68789687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863T>C
AA Mutation	p.Met288Thr(p.M288T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336440
Start	68790094:68790094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336440
Start	68789848:68789848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754764949
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336440
Start	68789738:68789738(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.812delG
AA Mutation	p.Gly271ValfsTer36(p.G271Vfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336440
Start	68789671:68789671(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.879delC
AA Mutation	p.Ser294AlafsTer13(p.S294Afs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336440
Start	68790021:68790021(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.529delC
AA Mutation	p.His177ThrfsTer56(p.H177Tfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336440
Start	68789729:68789729(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.821delC
AA Mutation	p.Pro274ArgfsTer33(p.P274Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZFP36L1

No Mutation Annotation!