Colon Cancer: Gene >> NCAPH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000240423
Start	96341699:96341699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77C>T
AA Mutation	p.Ala26Val(p.A26V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000240423
Start	96367273:96367273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1898T>C
AA Mutation	p.Ile633Thr(p.I633T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000240423
Start	96359067:96359067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1231G>A
AA Mutation	p.Asp411Asn(p.D411N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000240423
Start	96344216:96344216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752350518
CDS Mutation	c.707A>G
AA Mutation	p.Asp236Gly(p.D236G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000240423
Start	96369000:96369000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774780229
CDS Mutation	c.2027C>T
AA Mutation	p.Ala676Val(p.A676V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000240423
Start	96360606:96360606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483A>G
AA Mutation	p.Lys495Glu(p.K495E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000240423
Start	96360190:96360190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1405G>A
AA Mutation	p.Asp469Asn(p.D469N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000240423
Start	96364562:96364562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1669G>A
AA Mutation	p.Asp557Asn(p.D557N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000240423
Start	96341783:96341783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161A>C
AA Mutation	p.Asp54Ala(p.D54A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240423
Start	96344220:96344220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240423
Start	96344142:96344142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240423
Start	96366001:96366001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1824C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240423
Start	96369019:96369019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2046T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240423
Start	96365884:96365884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1707C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000240423
Start	96360183:96360183(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1404delA
AA Mutation	p.Asp469IlefsTer25(p.D469Ifs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NCAPH

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240423
Start	96354191:96354191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530283845
CDS Mutation	c.1011G>A
Mutation Classification	Silent
Feature Type	Transcript