Colon Cancer: Gene >> NDE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396355
Start	15667401:15667401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765611446
CDS Mutation	c.199G>A
AA Mutation	p.Glu67Lys(p.E67K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396355
Start	15691150:15691150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530G>A
AA Mutation	p.Arg177Gln(p.R177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396355
Start	15694209:15694209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Trp(p.R250W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396355
Start	15664791:15664791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536800933
CDS Mutation	c.13G>A
AA Mutation	p.Gly5Arg(p.G5R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396355
Start	15694236:15694236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>A
AA Mutation	p.Asp259Asn(p.D259N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000396355
Start	15677949:15677949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761910819
CDS Mutation	c.386G>A
AA Mutation	p.Arg129His(p.R129H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396355
Start	15694205:15694205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1123418
CDS Mutation	c.744G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396355
Start	15677866:15677866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779987698
CDS Mutation	c.303G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396355
Start	15694253:15694253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396355
Start	15677836:15677836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396355
Start	15694189:15694189(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749768828
CDS Mutation	c.733delC
AA Mutation	p.Leu245SerfsTer113(p.L245Sfs*113)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396355
Start	15691192:15691192(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.576delC
AA Mutation	p.Met193CysfsTer34(p.M193Cfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396355
Start	15694188:15694189(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.733dupC
AA Mutation	p.Leu245ProfsTer70(p.L245Pfs*70)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000396355
Start	15667441:15667441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NDE1

No Mutation Annotation!