Colon Cancer: Gene >> BTBD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378226
Start	11923345:11923345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1248C>A
AA Mutation	p.Ser416Arg(p.S416R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378226
Start	11923268:11923268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171C>T
AA Mutation	p.Arg391Cys(p.R391C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378226
Start	11923260:11923260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1163G>T
AA Mutation	p.Trp388Leu(p.W388L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378226
Start	11919829:11919829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150544423
CDS Mutation	c.529A>G
AA Mutation	p.Met177Val(p.M177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378226
Start	11923341:11923341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1244C>G
AA Mutation	p.Ser415Cys(p.S415C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378226
Start	11919091:11919091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332C>T
AA Mutation	p.Ala111Val(p.A111V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378226
Start	11922824:11922824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769315326
CDS Mutation	c.727C>T
AA Mutation	p.Arg243Cys(p.R243C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378226
Start	11918426:11918426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151G>A
AA Mutation	p.Glu51Lys(p.E51K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378226
Start	11919771:11919771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378226
Start	11923237:11923237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367831173
CDS Mutation	c.1140G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378226
Start	11918389:11918389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378226
Start	11923453:11923453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771415419
CDS Mutation	c.1356C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378226
Start	11923393:11923393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138082885
CDS Mutation	c.1296C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378226
Start	11923163:11923163(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1070delA
AA Mutation	p.Lys357SerfsTer7(p.K357Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378226
Start	11922708:11922709(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.611_612insAACATGTAAG
AA Mutation	p.Val205ThrfsTer13(p.V205Tfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BTBD3

No Mutation Annotation!