Colon Cancer: Gene >> GRIN2D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263269
Start	48441926:48441926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2410G>A
AA Mutation	p.Asp804Asn(p.D804N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263269
Start	48404920:48404920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652C>T
AA Mutation	p.Arg218Cys(p.R218C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263269
Start	48414575:48414575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1403G>A
AA Mutation	p.Arg468Gln(p.R468Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263269
Start	48442273:48442273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2564C>T
AA Mutation	p.Ala855Val(p.A855V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263269
Start	48405313:48405313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774247271
CDS Mutation	c.1045C>T
AA Mutation	p.Arg349Cys(p.R349C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263269
Start	48421875:48421875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752367785
CDS Mutation	c.2182G>A
AA Mutation	p.Asp728Asn(p.D728N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263269
Start	48419275:48419275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1777T>C
AA Mutation	p.Cys593Arg(p.C593R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263269
Start	48419702:48419702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1979T>C
AA Mutation	p.Leu660Pro(p.L660P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263269
Start	48414095:48414095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190C>G
AA Mutation	p.Thr397Arg(p.T397R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263269
Start	48416028:48416028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1608C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263269
Start	48405123:48405123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.855T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263269
Start	48442319:48442319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765264979
CDS Mutation	c.2610C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263269
Start	48421925:48421925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2232G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263269
Start	48441790:48441790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749410602
CDS Mutation	c.2274C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263269
Start	48441859:48441859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2343C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263269
Start	48405012:48405012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263269
Start	48442247:48442247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2538G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263269
Start	48414878:48414878(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1432delC
AA Mutation	p.Arg478AlafsTer15(p.R478Afs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263269
Start	48405161:48405161(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.898delC
AA Mutation	p.Leu300CysfsTer27(p.L300Cfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GRIN2D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263269
Start	48441923:48441923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2407A>G
AA Mutation	p.Ile803Val(p.I803V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263269
Start	48404949:48404949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531074073
CDS Mutation	c.681G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263269
Start	48416145:48416145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1725G>A
Mutation Classification	Silent
Feature Type	Transcript