Colon Cancer: Gene >> ZNF331

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53577633:53577633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1073C>A
AA Mutation	p.Thr358Lys(p.T358K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53577311:53577311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751A>G
AA Mutation	p.Thr251Ala(p.T251A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53576705:53576705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145T>C
AA Mutation	p.Ser49Pro(p.S49P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53571701:53571701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107T>C
AA Mutation	p.Leu36Pro(p.L36P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53577333:53577333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773T>C
AA Mutation	p.Leu258Pro(p.L258P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53571625:53571625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377282635
CDS Mutation	c.31G>A
AA Mutation	p.Val11Ile(p.V11I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53577554:53577554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.994T>C
AA Mutation	p.Cys332Arg(p.C332R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53577233:53577233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Trp(p.R225W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53577199:53577199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639A>C
AA Mutation	p.Lys213Asn(p.K213N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253144
Start	53577892:53577892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253144
Start	53577622:53577622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776670996
CDS Mutation	c.1062G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253144
Start	53577807:53577807(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1247delG
AA Mutation	p.Cys416LeufsTer36(p.C416Lfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253144
Start	53576736:53576736(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.182delA
AA Mutation	p.Asn61ThrfsTer5(p.N61Tfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	start_lost
Transcription ID	ENST00000253144
Start	53569378:53569378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	start_lost
Transcription ID	ENST00000253144
Start	53569377:53569377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF331

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53577924:53577924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752119475
CDS Mutation	c.1364G>A
AA Mutation	p.Arg455Gln(p.R455Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253144
Start	53577432:53577432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.872G>T
AA Mutation	p.Arg291Ile(p.R291I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253144
Start	53577892:53577892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253144
Start	53576736:53576736(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.182delA
AA Mutation	p.Asn61ThrfsTer5(p.N61Tfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000253144
Start	53577149:53577149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589C>T
AA Mutation	p.Arg197Ter(p.R197*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript