Colon Cancer: Gene >> KLHL34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21657095:21657095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694G>A
AA Mutation	p.Val232Ile(p.V232I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21656165:21656165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1624G>A
AA Mutation	p.Glu542Lys(p.E542K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21657299:21657299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Trp(p.R164W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21656927:21656927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.862C>T
AA Mutation	p.Arg288Cys(p.R288C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21656126:21656126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1663C>T
AA Mutation	p.Arg555Trp(p.R555W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21657385:21657385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404C>G
AA Mutation	p.Ala135Gly(p.A135G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21657646:21657646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143C>T
AA Mutation	p.Ala48Val(p.A48V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21656545:21656545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1244G>A
AA Mutation	p.Arg415Gln(p.R415Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21657586:21657586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203G>A
AA Mutation	p.Arg68His(p.R68H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21657220:21657220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569G>A
AA Mutation	p.Arg190Gln(p.R190Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21656116:21656116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1673C>A
AA Mutation	p.Pro558His(p.P558H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21656038:21656038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1751C>T
AA Mutation	p.Ser584Leu(p.S584L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21657655:21657655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.134C>T
AA Mutation	p.Ser45Leu(p.S45L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21656749:21656749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555586141
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347His(p.R347H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21657701:21657701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.88G>A
AA Mutation	p.Asp30Asn(p.D30N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21657262:21657262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.527C>T
AA Mutation	p.Pro176Leu(p.P176L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21656962:21656962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.827G>A
AA Mutation	p.Arg276Gln(p.R276Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379499
Start	21656772:21656772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379499
Start	21656589:21656589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761030508
CDS Mutation	c.1200G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379499
Start	21657702:21657702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379499
Start	21657750:21657750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379499
Start	21656409:21656409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745809754
CDS Mutation	c.1380G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379499
Start	21656694:21656694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1095C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379499
Start	21657699:21657699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761882723
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379499
Start	21656166:21656166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1623C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379499
Start	21656928:21656928(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763678878
CDS Mutation	c.861delG
AA Mutation	p.Arg288AlafsTer7(p.R288Afs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000379499
Start	21657516:21657516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273G>A
AA Mutation	p.Trp91Ter(p.W91*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000379499
Start	21656189:21656189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1600C>T
AA Mutation	p.Arg534Ter(p.R534*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KLHL34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379499
Start	21657664:21657664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125C>T
AA Mutation	p.Ala42Val(p.A42V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript