Colon Cancer: Gene >> KLHL29

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23703221:23703221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2141C>G
AA Mutation	p.Ala714Gly(p.A714G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23642662:23642662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.752C>A
AA Mutation	p.Ala251Asp(p.A251D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23695651:23695651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1571G>A
AA Mutation	p.Arg524His(p.R524H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23562320:23562320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124G>A
AA Mutation	p.Gly42Ser(p.G42S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23642478:23642478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568C>T
AA Mutation	p.Pro190Ser(p.P190S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23691872:23691872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1278T>A
AA Mutation	p.Phe426Leu(p.F426L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23691873:23691873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1279C>A
AA Mutation	p.Leu427Ile(p.L427I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23693426:23693426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1440C>A
AA Mutation	p.Phe480Leu(p.F480L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23639193:23639193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340C>T
AA Mutation	p.Arg114Trp(p.R114W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23695630:23695630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1550C>G
AA Mutation	p.Ala517Gly(p.A517G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000486442
Start	23695742:23695742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529955357
CDS Mutation	c.1662C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000486442
Start	23695652:23695652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000486442
Start	23693420:23693420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000486442
Start	23562469:23562469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552154531
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000486442
Start	23642831:23642831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KLHL29

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000486442
Start	23693426:23693426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1440C>A
AA Mutation	p.Phe480Leu(p.F480L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript