Colon Cancer: Gene >> WNT9A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272164
Start	227925407:227925407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763194335
CDS Mutation	c.208C>T
AA Mutation	p.Arg70Cys(p.R70C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272164
Start	227921658:227921658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761246906
CDS Mutation	c.958G>A
AA Mutation	p.Glu320Lys(p.E320K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272164
Start	227921792:227921792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149631380
CDS Mutation	c.824C>T
AA Mutation	p.Ser275Leu(p.S275L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272164
Start	227921961:227921961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655G>A
AA Mutation	p.Gly219Ser(p.G219S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000272164
Start	227924248:227924248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>A
AA Mutation	p.Gly169Arg(p.G169R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000272164
Start	227921775:227921775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779996471
CDS Mutation	c.841G>A
AA Mutation	p.Asp281Asn(p.D281N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000272164
Start	227924319:227924319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139076976
CDS Mutation	c.434G>A
AA Mutation	p.Arg145His(p.R145H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000272164
Start	227921916:227921916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700G>A
AA Mutation	p.Ala234Thr(p.A234T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000272164
Start	227924299:227924299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768643974
CDS Mutation	c.454G>A
AA Mutation	p.Asp152Asn(p.D152N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000272164
Start	227921639:227921639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768307025
CDS Mutation	c.977G>A
AA Mutation	p.Arg326His(p.R326H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272164
Start	227921698:227921698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141731322
CDS Mutation	c.918G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272164
Start	227924297:227924297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272164
Start	227924234:227924234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272164
Start	227921830:227921830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756129922
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272164
Start	227921731:227921731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191187721
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272164
Start	227924253:227924253(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.500delG
AA Mutation	p.Gly167AlafsTer38(p.G167Afs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000272164
Start	227921541:227921541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075G>T
AA Mutation	p.Glu359Ter(p.E359*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> WNT9A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272164
Start	227924348:227924348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147711960
CDS Mutation	c.405C>T
Mutation Classification	Silent
Feature Type	Transcript