Colon Cancer: Gene >> ZBTB10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000430430
Start	80499598:80499598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1077G>T
AA Mutation	p.Lys359Asn(p.K359N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000430430
Start	80487145:80487145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335G>C
AA Mutation	p.Gly112Ala(p.G112A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000430430
Start	80499567:80499567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046A>G
AA Mutation	p.Gln349Arg(p.Q349R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000430430
Start	80499966:80499966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1445G>A
AA Mutation	p.Arg482Lys(p.R482K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430430
Start	80499724:80499724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1203T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430430
Start	80500090:80500090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771403721
CDS Mutation	c.1569C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430430
Start	80518512:80518512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2070T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000430430
Start	80487515:80487515(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.705delG
AA Mutation	p.Leu236SerfsTer7(p.L236Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000430430
Start	80518847:80518847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2203C>T
AA Mutation	p.Arg735Ter(p.R735*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000430430
Start	80519502:80519502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2590G>T
AA Mutation	p.Glu864Ter(p.E864*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000430430
Start	80487554:80487556(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.746_748delCCT
AA Mutation	p.Ser249del(p.S249del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZBTB10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000430430
Start	80499504:80499504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983T>G
AA Mutation	p.Ile328Arg(p.I328R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430430
Start	80499550:80499550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430430
Start	80499952:80499952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431G>A
Mutation Classification	Silent
Feature Type	Transcript