Colon Cancer: Gene >> VGLL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370634
Start	136548666:136548666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>T
AA Mutation	p.Arg98Cys(p.R98C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370634
Start	136548686:136548686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.312G>C
AA Mutation	p.Leu104Phe(p.L104F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370634
Start	136548610:136548610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.236A>T
AA Mutation	p.Gln79Leu(p.Q79L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370634
Start	136550772:136550772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639G>T
AA Mutation	p.Lys213Asn(p.K213N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370634
Start	136536097:136536097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370153819
CDS Mutation	c.77G>A
AA Mutation	p.Arg26Gln(p.R26Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370634
Start	136548710:136548710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.336G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370634
Start	136548929:136548929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749163851
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370634
Start	136536212:136536212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VGLL1

No Mutation Annotation!