Colon Cancer: Gene >> MICALL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215957
Start	37906491:37906491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.69G>T
AA Mutation	p.Glu23Asp(p.E23D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215957
Start	37925866:37925866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1288G>A
AA Mutation	p.Glu430Lys(p.E430K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215957
Start	37931845:37931845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1928C>A
AA Mutation	p.Ala643Glu(p.A643E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000215957
Start	37919151:37919151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.542G>A
AA Mutation	p.Gly181Asp(p.G181D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000215957
Start	37927744:37927744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1799C>T
AA Mutation	p.Ala600Val(p.A600V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000215957
Start	37937154:37937154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2383C>T
AA Mutation	p.Arg795Cys(p.R795C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215957
Start	37912422:37912422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146083250
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215957
Start	37912413:37912413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215957
Start	37919053:37919053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000215957
Start	37922132:37922132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730C>T
AA Mutation	p.Gln244Ter(p.Q244*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000215957
Start	37932889:37932889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2234+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MICALL1

No Mutation Annotation!