Colon Cancer: Gene >> FZD10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130163724:130163724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782G>A
AA Mutation	p.Arg261His(p.R261H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130164120:130164120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178C>T
AA Mutation	p.Ala393Val(p.A393V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130163330:130163330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388G>T
AA Mutation	p.Asp130Tyr(p.D130Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130164162:130164162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220T>C
AA Mutation	p.Val407Ala(p.V407A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130163606:130163606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374628122
CDS Mutation	c.664G>A
AA Mutation	p.Glu222Lys(p.E222K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130164294:130164294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1352A>G
AA Mutation	p.Tyr451Cys(p.Y451C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130164167:130164167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1225G>A
AA Mutation	p.Gly409Ser(p.G409S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130163217:130163217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275C>T
AA Mutation	p.Ala92Val(p.A92V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130163733:130163733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791T>C
AA Mutation	p.Ile264Thr(p.I264T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130163564:130163564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622G>A
AA Mutation	p.Ala208Thr(p.A208T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130163669:130163669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130164303:130164303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1361C>T
AA Mutation	p.Pro454Leu(p.P454L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130164060:130164060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770701893
CDS Mutation	c.1118G>A
AA Mutation	p.Arg373His(p.R373H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130162973:130162973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31G>T
AA Mutation	p.Val11Phe(p.V11F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130163097:130163097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.155T>C
AA Mutation	p.Met52Thr(p.M52T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229030
Start	130163029:130163029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747697911
CDS Mutation	c.87G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229030
Start	130164076:130164076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229030
Start	130163605:130163605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229030
Start	130164427:130164427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1485C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229030
Start	130162996:130162996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.54C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000229030
Start	130163632:130163632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.690G>A
AA Mutation	p.Trp230Ter(p.W230*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FZD10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130163781:130163781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839G>A
AA Mutation	p.Arg280His(p.R280H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130163132:130163132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754557108
CDS Mutation	c.190G>A
AA Mutation	p.Ala64Thr(p.A64T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229030
Start	130164077:130164077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1135G>A
AA Mutation	p.Glu379Lys(p.E379K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229030
Start	130164193:130164193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775924759
CDS Mutation	c.1251C>T
Mutation Classification	Silent
Feature Type	Transcript