Colon Cancer: Gene >> DENND1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6470362:6470362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1295G>C
AA Mutation	p.Gly432Ala(p.G432A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6479003:6479003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.230C>T
AA Mutation	p.Ala77Val(p.A77V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6475719:6475719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812C>T
AA Mutation	p.Ala271Val(p.A271V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6470315:6470315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373788641
CDS Mutation	c.1342G>A
AA Mutation	p.Val448Ile(p.V448I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6475380:6475380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751299679
CDS Mutation	c.947G>A
AA Mutation	p.Arg316Gln(p.R316Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6476909:6476909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626C>T
AA Mutation	p.Ala209Val(p.A209V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6472929:6472929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118C>T
AA Mutation	p.Ala373Val(p.A373V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6470354:6470354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536993980
CDS Mutation	c.1303G>A
AA Mutation	p.Ala435Thr(p.A435T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6467826:6467826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2084C>T
AA Mutation	p.Ala695Val(p.A695V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6469621:6469621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1382G>A
AA Mutation	p.Gly461Glu(p.G461E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381480
Start	6467783:6467783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2127G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381480
Start	6471440:6471440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761187263
CDS Mutation	c.1215C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381480
Start	6468369:6468369(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1656delG
AA Mutation	p.Ser553LeufsTer8(p.S553Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381480
Start	6468925:6468925(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1436delG
AA Mutation	p.Gly479AlafsTer3(p.G479Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381480
Start	6479895:6479895(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs757060526
CDS Mutation	c.90delC
AA Mutation	p.Ile31SerfsTer81(p.I31Sfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000381480
Start	6471431:6471433(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs774558415
CDS Mutation	c.1222_1224delGAG
AA Mutation	p.Glu408del(p.E408del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DENND1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6475900:6475900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.716A>G
AA Mutation	p.Tyr239Cys(p.Y239C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6467755:6467755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2155C>A
AA Mutation	p.Leu719Met(p.L719M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6478839:6478839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310T>C
AA Mutation	p.Phe104Leu(p.F104L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381480
Start	6479696:6479696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149A>C
AA Mutation	p.Lys50Thr(p.K50T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381480
Start	6470355:6470355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370304063
CDS Mutation	c.1302C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381480
Start	6467837:6467837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2073A>G
Mutation Classification	Silent
Feature Type	Transcript