Colon Cancer: Gene >> ARID4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235252776:235252776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781028340
CDS Mutation	c.308G>A
AA Mutation	p.Arg103Gln(p.R103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235181656:235181656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768130451
CDS Mutation	c.3263C>T
AA Mutation	p.Ser1088Leu(p.S1088L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235181856:235181856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3063T>G
AA Mutation	p.Asn1021Lys(p.N1021K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235219854:235219854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1522A>G
AA Mutation	p.Thr508Ala(p.T508A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235219946:235219946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1430A>C
AA Mutation	p.Glu477Ala(p.E477A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264183
Start	235213870:235213870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1740A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264183
Start	235194151:235194151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1987C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264183
Start	235182051:235182051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780783351
CDS Mutation	c.2868G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264183
Start	235255673:235255673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264183
Start	235220414:235220414(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1295delA
AA Mutation	p.Asn432MetfsTer8(p.N432Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264183
Start	235182104:235182104(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2815delA
AA Mutation	p.Thr939ArgfsTer2(p.T939Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000264183
Start	235182110:235182110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2809A>T
AA Mutation	p.Lys937Ter(p.K937*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264183
Start	235194161:235194162(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1976dupA
AA Mutation	p.Asn659LysfsTer3(p.N659Kfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARID4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235172723:235172723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3706C>A
AA Mutation	p.Leu1236Ile(p.L1236I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264183
Start	235224736:235224736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937C>A
AA Mutation	p.Leu313Ile(p.L313I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264183
Start	235182104:235182104(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2815delA
AA Mutation	p.Thr939ArgfsTer2(p.T939Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript