Colon Cancer: Gene >> ANKRD6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000339746
Start	89627646:89627646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780403490
CDS Mutation	c.1435C>T
AA Mutation	p.Arg479Cys(p.R479C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000339746
Start	89624031:89624031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375712466
CDS Mutation	c.1192C>T
AA Mutation	p.Arg398Trp(p.R398W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000339746
Start	89606067:89606067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379C>T
AA Mutation	p.Leu127Phe(p.L127F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000339746
Start	89621944:89621944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.815G>A
AA Mutation	p.Arg272Gln(p.R272Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000339746
Start	89603083:89603083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747899705
CDS Mutation	c.274G>A
AA Mutation	p.Ala92Thr(p.A92T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000339746
Start	89630820:89630820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2000T>G
AA Mutation	p.Leu667Arg(p.L667R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000339746
Start	89630892:89630892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747160750
CDS Mutation	c.2072G>A
AA Mutation	p.Arg691Gln(p.R691Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000339746
Start	89624558:89624558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238G>A
AA Mutation	p.Arg413Gln(p.R413Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000339746
Start	89630715:89630715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200289900
CDS Mutation	c.1895G>A
AA Mutation	p.Arg632His(p.R632H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339746
Start	89630644:89630644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1824G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339746
Start	89621960:89621960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.831G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000522441
Start	89621949:89621949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375403975
CDS Mutation	c.820C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000339746
Start	89630830:89630830(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs757124885
CDS Mutation	c.2016delT
AA Mutation	p.Phe672LeufsTer34(p.F672Lfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ANKRD6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000339746
Start	89613839:89613839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564C>A
Mutation Classification	Silent
Feature Type	Transcript