Colon Cancer: Gene >> ANKRD36B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258459
Start	97585063:97585063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765994654
CDS Mutation	c.331G>A
AA Mutation	p.Asp111Asn(p.D111N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258459
Start	97541919:97541919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1877G>A
AA Mutation	p.Arg626His(p.R626H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000258459
Start	97585116:97585116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278C>T
AA Mutation	p.Ala93Val(p.A93V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258459
Start	97538215:97538215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2042T>A
AA Mutation	p.Leu681His(p.L681H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258459
Start	97541965:97541965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1831G>T
AA Mutation	p.Asp611Tyr(p.D611Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258459
Start	97545686:97545686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1661A>C
AA Mutation	p.Asp554Ala(p.D554A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258459
Start	97580468:97580468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551T>C
AA Mutation	p.Leu184Pro(p.L184P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258459
Start	97556956:97556956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772956561
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258459
Start	97580542:97580542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.477T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258459
Start	97523375:97523375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2358T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258459
Start	97551332:97551332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550556385
CDS Mutation	c.1332G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ANKRD36B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258459
Start	97547596:97547596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768690692
CDS Mutation	c.1519G>A
AA Mutation	p.Glu507Lys(p.E507K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258459
Start	97551463:97551463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291C>A
AA Mutation	p.Pro431Thr(p.P431T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258459
Start	97515818:97515818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2535A>G
Mutation Classification	Silent
Feature Type	Transcript