Colon Cancer: Gene >> MPP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398389
Start	43801853:43801853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1606G>A
AA Mutation	p.Ala536Thr(p.A536T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398389
Start	43814352:43814352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1019G>A
AA Mutation	p.Arg340Gln(p.R340Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000398389
Start	43824005:43824005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610G>A
AA Mutation	p.Ala204Thr(p.A204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398389
Start	43829725:43829725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370G>A
AA Mutation	p.Asp124Asn(p.D124N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398389
Start	43814296:43814296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075A>G
AA Mutation	p.Met359Val(p.M359V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398389
Start	43814257:43814257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1114G>A
AA Mutation	p.Glu372Lys(p.E372K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398389
Start	43809066:43809066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398389
Start	43818074:43818074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770195012
CDS Mutation	c.918G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398389
Start	43825777:43825777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375141612
CDS Mutation	c.588C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398389
Start	43820936:43820936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141959648
CDS Mutation	c.807G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398389
Start	43825774:43825774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.591C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398389
Start	43814024:43814024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398389
Start	43831579:43831579(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.124delA
AA Mutation	p.Ser42AlafsTer5(p.S42Afs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MPP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398389
Start	43831588:43831588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.115A>G
AA Mutation	p.Ser39Gly(p.S39G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000398389
Start	43825812:43825812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.553G>T
AA Mutation	p.Glu185Ter(p.E185*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript