Colon Cancer: Gene >> PIDD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347755
Start	804326:804326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.63G>T
AA Mutation	p.Glu21Asp(p.E21D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347755
Start	800359:800359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769334697
CDS Mutation	c.2134C>T
AA Mutation	p.Arg712Trp(p.R712W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347755
Start	804181:804181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.208A>C
AA Mutation	p.Ser70Arg(p.S70R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000347755
Start	800769:800769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1910G>A
AA Mutation	p.Arg637Gln(p.R637Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000347755
Start	800406:800406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752167351
CDS Mutation	c.2087C>T
AA Mutation	p.Ser696Leu(p.S696L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000347755
Start	804345:804345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44C>T
AA Mutation	p.Ala15Val(p.A15V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000347755
Start	802748:802748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756216117
CDS Mutation	c.853G>A
AA Mutation	p.Ala285Thr(p.A285T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000347755
Start	799555:799555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2485G>A
AA Mutation	p.Asp829Asn(p.D829N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000347755
Start	800809:800809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1870C>T
AA Mutation	p.Arg624Cys(p.R624C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000347755
Start	804194:804194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195A>C
AA Mutation	p.Glu65Asp(p.E65D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347755
Start	800167:800167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145480879
CDS Mutation	c.2238C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347755
Start	801249:801249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377081340
CDS Mutation	c.1599C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347755
Start	800658:800658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1926C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347755
Start	802704:802704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347755
Start	804301:804301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.88C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347755
Start	800206:800206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774016396
CDS Mutation	c.2199C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PIDD1

No Mutation Annotation!