Colon Cancer: Gene >> ALS2CL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46681533:46681533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777220274
CDS Mutation	c.1241G>A
AA Mutation	p.Arg414Gln(p.R414Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46683257:46683257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.982C>A
AA Mutation	p.Leu328Met(p.L328M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46681540:46681540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234C>A
AA Mutation	p.His412Asn(p.H412N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46683239:46683239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1000C>A
AA Mutation	p.Pro334Thr(p.P334T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46671052:46671052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2794C>T
AA Mutation	p.His932Tyr(p.H932Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46681560:46681560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1214A>C
AA Mutation	p.Lys405Thr(p.K405T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46671501:46671501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2768T>C
AA Mutation	p.Leu923Pro(p.L923P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46677012:46677012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200208936
CDS Mutation	c.1768G>A
AA Mutation	p.Val590Met(p.V590M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46685577:46685577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753736240
CDS Mutation	c.734C>T
AA Mutation	p.Pro245Leu(p.P245L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46672159:46672159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775618276
CDS Mutation	c.2515G>A
AA Mutation	p.Glu839Lys(p.E839K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46676921:46676921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1859A>C
AA Mutation	p.Glu620Ala(p.E620A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46679260:46679260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1576G>A
AA Mutation	p.Asp526Asn(p.D526N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46686435:46686435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539A>C
AA Mutation	p.His180Pro(p.H180P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46687083:46687083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376089110
CDS Mutation	c.434C>T
AA Mutation	p.Ser145Leu(p.S145L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46687117:46687117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761173942
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Trp(p.R134W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318962
Start	46681398:46681398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201259046
CDS Mutation	c.1284C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318962
Start	46676331:46676331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777723802
CDS Mutation	c.2100C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318962
Start	46682076:46682076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1128G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318962
Start	46680442:46680442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760332683
CDS Mutation	c.1536G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318962
Start	46680499:46680499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115756496
CDS Mutation	c.1479C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	start_lost
Transcription ID	ENST00000318962
Start	46689440:46689440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ALS2CL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318962
Start	46671962:46671962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2606C>T
AA Mutation	p.Ser869Leu(p.S869L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript