Mutation

Primary Site >> Stomach Cancer

Gene >> PRDM16

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3186416:3186416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329T>C
AA Mutation	p.Leu110Pro(p.L110P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411456:3411456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752753184
CDS Mutation	c.1259G>A
AA Mutation	p.Arg420His(p.R420H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411722:3411722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374937969
CDS Mutation	c.1525G>A
AA Mutation	p.Ala509Thr(p.A509T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3402823:3402823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764674939
CDS Mutation	c.709G>A
AA Mutation	p.Glu237Lys(p.E237K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411449:3411449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781605949
CDS Mutation	c.1252G>A
AA Mutation	p.Asp418Asn(p.D418N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411446:3411446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249G>A
AA Mutation	p.Ala417Thr(p.A417T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3417933:3417933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371460126
CDS Mutation	c.2797C>T
AA Mutation	p.Arg933Trp(p.R933W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3426216:3426216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3275C>T
AA Mutation	p.Thr1092Ile(p.T1092I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3425637:3425637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2996G>A
AA Mutation	p.Arg999Gln(p.R999Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3412457:3412457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369599647
CDS Mutation	c.2260G>A
AA Mutation	p.Glu754Lys(p.E754K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3402806:3402806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692G>A
AA Mutation	p.Arg231His(p.R231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411986:3411986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753255714
CDS Mutation	c.1789G>A
AA Mutation	p.Asp597Asn(p.D597N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3186136:3186136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183153140
CDS Mutation	c.49G>A
AA Mutation	p.Val17Ile(p.V17I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411771:3411771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373011563
CDS Mutation	c.1574G>A
AA Mutation	p.Arg525Gln(p.R525Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3418716:3418716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2911A>T
AA Mutation	p.Arg971Trp(p.R971W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411934:3411934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737C>G
AA Mutation	p.Phe579Leu(p.F579L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411827:3411827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1630G>A
AA Mutation	p.Asp544Asn(p.D544N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000270722
Start	3411923:3411923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201517929
CDS Mutation	c.1726G>A
AA Mutation	p.Glu576Lys(p.E576K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3430953:3430953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370195954
CDS Mutation	c.3366C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3432008:3432008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3564G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3402984:3402984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3405599:3405599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748323433
CDS Mutation	c.1137C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3412420:3412420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756779855
CDS Mutation	c.2223G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3412540:3412540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2343C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3411775:3411775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376747653
CDS Mutation	c.1578G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3433778:3433778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3798G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3426187:3426187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3246T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3402945:3402945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3412186:3412186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1989C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3186417:3186417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3426139:3426139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541579138
CDS Mutation	c.3198C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3417884:3417884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370768364
CDS Mutation	c.2748G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270722
Start	3405590:3405590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1128C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270722
Start	3411588:3411588(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1395delC
AA Mutation	p.Ser466AlafsTer3(p.S466Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000270722
Start	3412411:3412411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2214C>A
AA Mutation	p.Tyr738Ter(p.Y738*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270722
Start	3418684:3418685(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2883dupC
AA Mutation	p.Arg962GlnfsTer21(p.R962Qfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript