Colon Cancer: Gene >> PPP1R13L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45385951:45385951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1954G>A
AA Mutation	p.Asp652Asn(p.D652N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45395649:45395649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1141G>A
AA Mutation	p.Ala381Thr(p.A381T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45385711:45385711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2099C>T
AA Mutation	p.Ala700Val(p.A700V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45396422:45396422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727C>T
AA Mutation	p.Arg243Cys(p.R243C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000360957
Start	45396338:45396338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811C>T
AA Mutation	p.Arg271Cys(p.R271C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360957
Start	45391924:45391924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1771C>T
AA Mutation	p.Pro591Ser(p.P591S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45398026:45398026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372792420
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45396357:45396357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.792G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360957
Start	45395860:45395860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560618631
CDS Mutation	c.930G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360957
Start	45395472:45395472(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1318delC
AA Mutation	p.Gln440SerfsTer10(p.Q440Sfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360957
Start	45392011:45392012(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs780494005
CDS Mutation	c.1683dupG
AA Mutation	p.Pro562AlafsTer10(p.P562Afs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PPP1R13L

No Mutation Annotation!