Colon Cancer: Gene >> YY2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000429584
Start	21857508:21857508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024G>A
AA Mutation	p.Val342Met(p.V342M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000429584
Start	21857092:21857092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608A>T
AA Mutation	p.Gln203Leu(p.Q203L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000429584
Start	21856686:21856686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.202A>G
AA Mutation	p.Asn68Asp(p.N68D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429584
Start	21857057:21857057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429584
Start	21857021:21857021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429584
Start	21856889:21856889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429584
Start	21856676:21856676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773669593
CDS Mutation	c.192G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429584
Start	21856973:21856973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429584
Start	21856706:21856706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762811083
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000429584
Start	21856899:21856899(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.419delA
AA Mutation	p.Lys140SerfsTer46(p.K140Sfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000429584
Start	21857148:21857148(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.669delG
AA Mutation	p.Leu224TyrfsTer18(p.L224Yfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> YY2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429584
Start	21857057:21857057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429584
Start	21856982:21856982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498G>A
Mutation Classification	Silent
Feature Type	Transcript