Colon Cancer: Gene >> MBD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249910
Start	129437905:129437905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150G>T
AA Mutation	p.Glu50Asp(p.E50D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000249910
Start	129431578:129431578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1666G>A
AA Mutation	p.Val556Met(p.V556M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249910
Start	129437916:129437916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755035506
CDS Mutation	c.139G>A
AA Mutation	p.Gly47Arg(p.G47R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249910
Start	129433140:129433140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1519G>A
AA Mutation	p.Gly507Ser(p.G507S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000249910
Start	129433125:129433125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1534C>T
AA Mutation	p.Arg512Trp(p.R512W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000249910
Start	129436899:129436899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745G>A
AA Mutation	p.Gly249Arg(p.G249R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000249910
Start	129433102:129433102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1557C>A
AA Mutation	p.Phe519Leu(p.F519L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000249910
Start	129437252:129437252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371283287
CDS Mutation	c.392A>G
AA Mutation	p.Asn131Ser(p.N131S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249910
Start	129437251:129437251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753080632
CDS Mutation	c.393T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000249910
Start	129436705:129436706(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.938_939delAA
AA Mutation	p.Lys313ArgfsTer13(p.K313Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000249910
Start	129433972:129433972(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1289delC
AA Mutation	p.Pro430HisfsTer61(p.P430Hfs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000249910
Start	129436705:129436705(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747480541
CDS Mutation	c.939delA
AA Mutation	p.Glu314LysfsTer4(p.E314Kfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MBD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249910
Start	129431549:129431549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1695A>C
AA Mutation	p.Lys565Asn(p.K565N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249910
Start	129436721:129436721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923G>A
AA Mutation	p.Ser308Asn(p.S308N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript