Colon Cancer: Gene >> STARD13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33129504:33129504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1173G>T
AA Mutation	p.Glu391Asp(p.E391D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33111869:33111869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2516C>A
AA Mutation	p.Thr839Asn(p.T839N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33129434:33129434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243C>A
AA Mutation	p.Leu415Ile(p.L415I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33118168:33118168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2178G>T
AA Mutation	p.Gln726His(p.Q726H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33106924:33106924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3058A>G
AA Mutation	p.Thr1020Ala(p.T1020A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33129601:33129601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200449699
CDS Mutation	c.1076G>A
AA Mutation	p.Arg359His(p.R359H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33127494:33127494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1801G>T
AA Mutation	p.Ala601Ser(p.A601S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33130216:33130216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461C>A
AA Mutation	p.Ser154Tyr(p.S154Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33110740:33110740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2775C>A
AA Mutation	p.Phe925Leu(p.F925L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33106874:33106874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3108T>G
AA Mutation	p.His1036Gln(p.H1036Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000336934
Start	33129658:33129658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375291281
CDS Mutation	c.1019G>A
AA Mutation	p.Ser340Asn(p.S340N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336934
Start	33127420:33127420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1875G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336934
Start	33129735:33129735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559223209
CDS Mutation	c.942G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336934
Start	33109994:33109994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2926C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336934
Start	33130152:33130152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144505017
CDS Mutation	c.525G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336934
Start	33112849:33112849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769895350
CDS Mutation	c.2364G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336934
Start	33130059:33130059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766079318
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336934
Start	33129600:33129600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200783157
CDS Mutation	c.1077C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336934
Start	33106808:33106808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117237914
CDS Mutation	c.3174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336934
Start	33110031:33110031(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2889delC
AA Mutation	p.Ser964GlnfsTer4(p.S964Qfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336934
Start	33129969:33129969(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.708delC
AA Mutation	p.Arg237GlufsTer24(p.R237Efs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STARD13

No Mutation Annotation!