FOSB[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 147383	GRCh38/hg38 19q13.32-13.33(chr19:44971420-48257402)x3	PLA2G4C, PLA2G4C-AS1 +363 more	Copy number gain	See cases	GPathogenic
Select item 60278	GRCh38/hg38 19q13.32(chr19:45287256-45734078)x3	CKM, EML2 +69 more	Copy number gain	See cases	GUncertain significance
Select item 148766	GRCh38/hg38 19q13.32(chr19:45387389-46831000)x1	CALM3, CCDC61 +190 more	Copy number loss	See cases	GLikely pathogenic
Select item 785628	NM_006732.3(FOSB):c.97G>A (p.Gly33Ser)	FOSB (G33S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2459993	NM_006732.3(FOSB):c.136G>T (p.Gly46Cys)	FOSB (G46C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549502	NM_006732.3(FOSB):c.220A>G (p.Thr74Ala)	FOSB (T74A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233296	NM_006732.3(FOSB):c.284A>C (p.Asp95Ala)	FOSB (D95A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526354	NM_006732.3(FOSB):c.340A>C (p.Ser114Arg)	FOSB (S114R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248141	NM_006732.3(FOSB):c.371C>T (p.Ser124Phe)	FOSB (S124F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256975	NM_006732.3(FOSB):c.376A>G (p.Ser126Gly)	FOSB (S126G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096223	NM_006732.3(FOSB):c.379G>A (p.Gly127Arg)	FOSB (G127R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362533	NM_006732.3(FOSB):c.390T>G (p.Ser130Arg)	FOSB (S130R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315018	NM_006732.3(FOSB):c.394C>T (p.Pro132Ser)	FOSB (P132S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287436	NM_006732.3(FOSB):c.415C>G (p.Arg139Gly)	FOSB (R139G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226926	NM_006732.3(FOSB):c.416G>A (p.Arg139Gln)	FOSB (R139Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 757700	NM_006732.3(FOSB):c.537G>C (p.Leu179=)	FOSB	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3096224	NM_006732.3(FOSB):c.541G>C (p.Asp181His)	FOSB (D181H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295936	NM_006732.3(FOSB):c.541G>A (p.Asp181Asn)	FOSB (D181N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 762409	NM_006732.3(FOSB):c.660G>A (p.Pro220=)	FOSB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3096225	NM_006732.3(FOSB):c.670A>T (p.Ile224Phe)	FOSB (I188F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346039	NM_006732.3(FOSB):c.709G>A (p.Glu237Lys)	FOSB (E237K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509910	NM_006732.3(FOSB):c.759C>A (p.Ser253Arg)	FOSB (S217R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373927	NM_006732.3(FOSB):c.805A>G (p.Ser269Gly)	FOSB (S233G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290632	NM_006732.3(FOSB):c.818C>G (p.Pro273Arg)	FOSB (P237R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1526667	GRCh37/hg19 19q13.31-13.32(chr19:45074342-46133841)	APOC1, APOC2 +36 more	Copy number gain	not specified	GUncertain significance
Select item 816085	GRCh37/hg19 19q13.32-13.33(chr19:45531056-48174177)x3	GPR4, LOC400706 +75 more	Copy number gain	not provided	GUncertain significance
Select item 816084	GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3	CLDND2, IGSF23 +293 more	Copy number gain	not provided	GPathogenic
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ACP7, ACTMAP +434 more	Copy number gain	not provided	GPathogenic
Select item 564588	GRCh37/hg19 19q13.32(chr19:45945375-46215558)x3	EML2, SNRPD2 +10 more	Copy number gain	not provided	GUncertain significance
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	BICRA, BLOC1S3 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	A1BG, ABCA7 +1364 more	Copy number gain	See cases	GPathogenic
Select item 253776	GRCh37/hg19 19q13.32(chr19:45284576-45978239)x3	NECTIN2, APOE +24 more	Copy number gain	See cases	GUncertain significance
Select item 253540	GRCh37/hg19 19q13.2-13.32(chr19:43013365-47241534)x1	ERCC2, PPP5C +121 more	Copy number loss	See cases	GPathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 33