Colon Cancer: Gene >> DENND5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9178968:9178968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1561G>A
AA Mutation	p.Ala521Thr(p.A521T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9204164:9204164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445G>A
AA Mutation	p.Ala149Thr(p.A149T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9206711:9206711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375955901
CDS Mutation	c.253G>A
AA Mutation	p.Val85Ile(p.V85I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9203924:9203924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685G>A
AA Mutation	p.Ala229Thr(p.A229T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9142758:9142758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780628819
CDS Mutation	c.3475C>T
AA Mutation	p.Arg1159Trp(p.R1159W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9193657:9193657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760981468
CDS Mutation	c.974C>T
AA Mutation	p.Ala325Val(p.A325V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9141982:9141982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3638G>A
AA Mutation	p.Gly1213Asp(p.G1213D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9170759:9170759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1925G>A
AA Mutation	p.Arg642His(p.R642H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9165843:9165843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769758504
CDS Mutation	c.2276G>A
AA Mutation	p.Arg759His(p.R759H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9150744:9150744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148317700
CDS Mutation	c.2542C>T
AA Mutation	p.Arg848Cys(p.R848C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9142808:9142808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3425G>A
AA Mutation	p.Gly1142Asp(p.G1142D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9181011:9181011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1211A>C
AA Mutation	p.Lys404Thr(p.K404T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9178274:9178274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1764A>C
AA Mutation	p.Lys588Asn(p.K588N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9203699:9203699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.910T>G
AA Mutation	p.Cys304Gly(p.C304G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9204142:9204142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467T>C
AA Mutation	p.Met156Thr(p.M156T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9142757:9142757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200559278
CDS Mutation	c.3476G>A
AA Mutation	p.Arg1159Gln(p.R1159Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9145756:9145756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2917G>A
AA Mutation	p.Ala973Thr(p.A973T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328194
Start	9152365:9152365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2514T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328194
Start	9150132:9150132(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2684delA
AA Mutation	p.Lys895SerfsTer7(p.K895Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000328194
Start	9142845:9142845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3388C>T
AA Mutation	p.Arg1130Ter(p.R1130*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000328194
Start	9147146:9147146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2741T>G
AA Mutation	p.Leu914Ter(p.L914*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328194
Start	9150131:9150132(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2684dupA
AA Mutation	p.Leu896ValfsTer14(p.L896Vfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000328194
Start	9147028:9147028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2857+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DENND5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9147111:9147111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2776G>A
AA Mutation	p.Glu926Lys(p.E926K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9150744:9150744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148317700
CDS Mutation	c.2542C>T
AA Mutation	p.Arg848Cys(p.R848C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328194
Start	9203968:9203968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.641C>T
AA Mutation	p.Ser214Phe(p.S214F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328194
Start	9147067:9147067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568405118
CDS Mutation	c.2820C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328194
Start	9165911:9165911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11558093
CDS Mutation	c.2208C>T
Mutation Classification	Silent
Feature Type	Transcript