Colon Cancer: Gene >> PSKH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000291041
Start	67909654:67909654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747466620
CDS Mutation	c.905G>A
AA Mutation	p.Arg302His(p.R302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000291041
Start	67909594:67909594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845C>T
AA Mutation	p.Ala282Val(p.A282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000291041
Start	67909198:67909198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449T>C
AA Mutation	p.Val150Ala(p.V150A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000291041
Start	67927586:67927586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748229359
CDS Mutation	c.1219C>T
AA Mutation	p.Arg407Trp(p.R407W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000291041
Start	67909528:67909528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.779C>T
AA Mutation	p.Thr260Met(p.T260M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291041
Start	67927420:67927420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000291041
Start	67927395:67927395(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1028delG
AA Mutation	p.Arg343LeufsTer2(p.R343Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PSKH1

No Mutation Annotation!