Colon Cancer: Gene >> MYADM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336967
Start	53873845:53873845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316G>A
AA Mutation	p.Ala106Thr(p.A106T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336967
Start	53874113:53874113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584A>G
AA Mutation	p.Asn195Ser(p.N195S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336967
Start	53874334:53874334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.805G>A
AA Mutation	p.Gly269Ser(p.G269S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336967
Start	53874428:53874428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776582147
CDS Mutation	c.899C>T
AA Mutation	p.Thr300Met(p.T300M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336967
Start	53874472:53874472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767798672
CDS Mutation	c.943G>A
AA Mutation	p.Ala315Thr(p.A315T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336967
Start	53873927:53873927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775841521
CDS Mutation	c.398C>T
AA Mutation	p.Ser133Leu(p.S133L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336967
Start	53873944:53873944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415G>A
AA Mutation	p.Ala139Thr(p.A139T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336967
Start	53873665:53873665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136T>G
AA Mutation	p.Ser46Ala(p.S46A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336967
Start	53873939:53873939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410C>T
AA Mutation	p.Ala137Val(p.A137V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336967
Start	53874132:53874132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336967
Start	53873571:53873571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147345516
CDS Mutation	c.42G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336967
Start	53873697:53873697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756883060
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MYADM

No Mutation Annotation!