Colon Cancer: Gene >> MYBBP1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4554203:4554203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>C
AA Mutation	p.Val124Leu(p.V124L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4543059:4543059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145275737
CDS Mutation	c.2746G>A
AA Mutation	p.Asp916Asn(p.D916N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4539880:4539880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3522C>A
AA Mutation	p.Phe1174Leu(p.F1174L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4554198:4554198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.375G>T
AA Mutation	p.Lys125Asn(p.K125N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4543131:4543131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562871359
CDS Mutation	c.2674G>A
AA Mutation	p.Asp892Asn(p.D892N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4543118:4543118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181039881
CDS Mutation	c.2687G>A
AA Mutation	p.Arg896His(p.R896H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4541558:4541558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573540438
CDS Mutation	c.3202C>T
AA Mutation	p.Arg1068Cys(p.R1068C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4543047:4543047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747847889
CDS Mutation	c.2758G>A
AA Mutation	p.Ala920Thr(p.A920T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4541557:4541557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199584868
CDS Mutation	c.3203G>A
AA Mutation	p.Arg1068His(p.R1068H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4545276:4545276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561399448
CDS Mutation	c.2143C>T
AA Mutation	p.Arg715Trp(p.R715W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4545156:4545156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755542622
CDS Mutation	c.2180A>G
AA Mutation	p.Glu727Gly(p.E727G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4553839:4553839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200728167
CDS Mutation	c.532C>T
AA Mutation	p.Arg178Trp(p.R178W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4543113:4543113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2692G>T
AA Mutation	p.Gly898Trp(p.G898W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4541803:4541803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3176T>C
AA Mutation	p.Val1059Ala(p.V1059A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4548192:4548192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750166636
CDS Mutation	c.1675G>A
AA Mutation	p.Val559Met(p.V559M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4555146:4555146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.179A>G
AA Mutation	p.Tyr60Cys(p.Y60C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000254718
Start	4545671:4545671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754670204
CDS Mutation	c.2012G>A
AA Mutation	p.Arg671Gln(p.R671Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254718
Start	4550270:4550270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1107G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254718
Start	4548580:4548580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199791918
CDS Mutation	c.1500G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254718
Start	4541529:4541529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757893508
CDS Mutation	c.3231G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000254718
Start	4555145:4555145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180T>A
AA Mutation	p.Tyr60Ter(p.Y60*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000254718
Start	4554194:4554194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.378+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MYBBP1A

No Mutation Annotation!