Colon Cancer: Gene >> HNRNPD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313899
Start	82356811:82356811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838C>T
AA Mutation	p.Arg280Cys(p.R280C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313899
Start	82358752:82358752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.528A>C
AA Mutation	p.Lys176Asn(p.K176N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313899
Start	82358754:82358754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526A>C
AA Mutation	p.Lys176Gln(p.K176Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313899
Start	82358715:82358715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565C>A
AA Mutation	p.Leu189Ile(p.L189I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313899
Start	82355350:82355350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1052G>A
AA Mutation	p.Ser351Asn(p.S351N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313899
Start	82358816:82358816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.464T>C
AA Mutation	p.Met155Thr(p.M155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313899
Start	82373502:82373502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374147423
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313899
Start	82356601:82356601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000313899
Start	82373530:82373535(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.144_149delGGGCGG
AA Mutation	p.Gly49_Gly50del(p.G49_G50del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313899
Start	82355344:82355344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1058A>C
AA Mutation	p.Lys353Thr(p.K353T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313899
Start	82358752:82358752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.528A>C
AA Mutation	p.Lys176Asn(p.K176N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript