Colon Cancer: Gene >> PKMYT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262300
Start	2975724:2975724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467C>T
AA Mutation	p.Ala156Val(p.A156V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262300
Start	2976944:2976944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747789800
CDS Mutation	c.98G>A
AA Mutation	p.Arg33His(p.R33H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262300
Start	2975563:2975563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628G>A
AA Mutation	p.Val210Ile(p.V210I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262300
Start	2975467:2975467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724G>A
AA Mutation	p.Gly242Arg(p.G242R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262300
Start	2976881:2976881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554702940
CDS Mutation	c.161C>T
AA Mutation	p.Pro54Leu(p.P54L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262300
Start	2975331:2975331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761362077
CDS Mutation	c.860C>T
AA Mutation	p.Ala287Val(p.A287V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262300
Start	2976974:2976974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68G>A
AA Mutation	p.Gly23Asp(p.G23D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262300
Start	2975780:2975780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759932344
CDS Mutation	c.411G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262300
Start	2975435:2975435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542714330
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262300
Start	2975681:2975681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262300
Start	2976904:2976904(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.138delG
AA Mutation	p.Leu47SerfsTer92(p.L47Sfs*92)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PKMYT1

No Mutation Annotation!