Colon Cancer: Gene >> APC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233607
Start	1468911:1468911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5610G>T
AA Mutation	p.Lys1870Asn(p.K1870N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233607
Start	1466305:1466305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746737603
CDS Mutation	c.3004G>A
AA Mutation	p.Val1002Met(p.V1002M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233607
Start	1455469:1455469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608G>A
AA Mutation	p.Gly203Asp(p.G203D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233607
Start	1456381:1456381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793A>G
AA Mutation	p.Thr265Ala(p.T265A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233607
Start	1468988:1468988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768481261
CDS Mutation	c.5687C>A
AA Mutation	p.Ala1896Asp(p.A1896D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233607
Start	1460265:1460265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148440924
CDS Mutation	c.1388G>A
AA Mutation	p.Arg463His(p.R463H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000233607
Start	1466272:1466272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2971C>T
AA Mutation	p.Arg991Cys(p.R991C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000233607
Start	1467010:1467010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3709G>A
AA Mutation	p.Val1237Met(p.V1237M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000233607
Start	1468533:1468533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5232A>C
AA Mutation	p.Glu1744Asp(p.E1744D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000233607
Start	1466525:1466525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765851523
CDS Mutation	c.3224C>T
AA Mutation	p.Ser1075Leu(p.S1075L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233607
Start	1460818:1460818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368821154
CDS Mutation	c.1482C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233607
Start	1453531:1453531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375932325
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233607
Start	1466992:1466992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3691C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233607
Start	1466940:1466940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771423505
CDS Mutation	c.3639G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233607
Start	1466994:1466994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3693G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233607
Start	1457128:1457128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148333649
CDS Mutation	c.1092G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233607
Start	1465315:1465315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2014C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233607
Start	1466745:1466745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760286752
CDS Mutation	c.3444G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233607
Start	1468971:1468971(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5675delC
AA Mutation	p.Pro1892ArgfsTer104(p.P1892Rfs*104)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> APC2

No Mutation Annotation!