Colon Cancer: Gene >> ZNF35

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396056
Start	44659690:44659690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1327G>A
AA Mutation	p.Asp443Asn(p.D443N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396056
Start	44651093:44651093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26T>C
AA Mutation	p.Met9Thr(p.M9T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396056
Start	44659915:44659915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1552A>C
AA Mutation	p.Met518Leu(p.M518L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396056
Start	44659046:44659046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683G>T
AA Mutation	p.Gly228Val(p.G228V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396056
Start	44659330:44659330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745958143
CDS Mutation	c.967C>T
AA Mutation	p.Arg323Trp(p.R323W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396056
Start	44659013:44659013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650T>A
AA Mutation	p.Leu217His(p.L217H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396056
Start	44659831:44659831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1468A>G
AA Mutation	p.Thr490Ala(p.T490A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000396056
Start	44659760:44659760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397G>T
AA Mutation	p.Arg466Ile(p.R466I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000396056
Start	44652582:44652582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181680635
CDS Mutation	c.218C>T
AA Mutation	p.Ala73Val(p.A73V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396056
Start	44651139:44651139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753622014
CDS Mutation	c.72A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396056
Start	44659011:44659011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.648G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396056
Start	44659914:44659914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1551C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396056
Start	44658912:44658912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396056
Start	44659355:44659355(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.996delA
AA Mutation	p.Lys332AsnfsTer199(p.K332Nfs*199)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF35

No Mutation Annotation!