GLTPD2[gene] - ClinVar

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

Search results

Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154089	GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3	ABR, ABR-AS1 +962 more	Copy number gain	See cases	GPathogenic
Select item 153177	GRCh38/hg38 17p13.3-13.2(chr17:150732-5935377)x1	ABR, ABR-AS1 +463 more	Copy number loss	See cases	GPathogenic
Select item 149531	GRCh38/hg38 17p13.3-12(chr17:162016-12343901)x3	LOC130059883, LOC130059884 +922 more	Copy number gain	See cases	GPathogenic
Select item 149158	GRCh38/hg38 17p13.3-13.1(chr17:162016-7697012)x1	TRARG1, TRPV1 +651 more	Copy number loss	See cases	GPathogenic
Select item 144699	GRCh38/hg38 17p13.3-13.1(chr17:162088-6959050)x1	ABR, ABR-AS1 +498 more	Copy number loss	See cases	GPathogenic
Select item 2579287	GRCh38/hg38 17p13.3-12(chr17:165730-11404096)x3	SAT2, SCARF1 +911 more	Copy number gain	Chromosome 17p13.3 duplication syndrome	GPathogenic
Select item 59542	GRCh38/hg38 17p13.3-13.2(chr17:193307-5652222)x1	LOC121848004, LOC121848005 +457 more	Copy number loss	See cases	GPathogenic
Select item 145642	GRCh38/hg38 17p13.3-13.1(chr17:198748-7491129)x3	LOC130059937, LOC130059938 +604 more	Copy number gain	See cases	GPathogenic
Select item 144239	GRCh38/hg38 17p13.3-13.2(chr17:2062380-5258340)x1	CAMKK1, CAMTA2 +303 more	Copy number loss	See cases	GPathogenic
Select item 59563	GRCh38/hg38 17p13.2-13.1(chr17:3601515-7178024)x1	AIPL1, ALOX12 +290 more	Copy number loss	See cases	GPathogenic
Select item 146235	GRCh38/hg38 17p13.2(chr17:4044302-5943772)x1	ALOX15, ANKFY1 +166 more	Copy number loss	See cases	GLikely pathogenic
Select item 150854	GRCh38/hg38 17p13.2(chr17:4092608-5354473)x3	ALOX15, ANKFY1 +141 more	Copy number gain	See cases	GLikely benign
Select item 154947	GRCh38/hg38 17p13.2(chr17:4141725-4873241)x3	ALOX15, ANKFY1 +70 more	Copy number gain	See cases	GUncertain significance
Select item 1679759	Single allele	C17orf107, C17orf114 +68 more	Duplication	7p22.1 microduplication syndrome	GUncertain significance
Select item 2483853	NM_001014985.3(GLTPD2):c.17G>A (p.Arg6Gln)	GLTPD2 (R6Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338785	NM_001014985.3(GLTPD2):c.73C>G (p.Leu25Val)	GLTPD2 (L25V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281662	NM_001014985.3(GLTPD2):c.113G>T (p.Arg38Leu)	GLTPD2 (R74L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3281665	NM_001014985.3(GLTPD2):c.116C>T (p.Ser39Leu)	GLTPD2 (S75L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373559	NM_001014985.3(GLTPD2):c.134C>T (p.Ala45Val)	GLTPD2 (A45V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281664	NM_001014985.3(GLTPD2):c.142T>C (p.Cys48Arg)	GLTPD2 (C48R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486842	NM_001014985.3(GLTPD2):c.154G>C (p.Glu52Gln)	GLTPD2 (E52Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281663	NM_001014985.3(GLTPD2):c.236G>A (p.Arg79Gln)	GLTPD2 (R79Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3100379	NM_001014985.3(GLTPD2):c.242T>G (p.Met81Arg)	GLTPD2 (M117R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228235	NM_001014985.3(GLTPD2):c.243G>A (p.Met81Ile)	GLTPD2 (M81I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100380	NM_001014985.3(GLTPD2):c.368C>T (p.Ala123Val)	GLTPD2, LOC130060033 (A159V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371406	NM_001014985.3(GLTPD2):c.411G>T (p.Glu137Asp)	GLTPD2, LOC130060033 (E173D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466597	NM_001014985.3(GLTPD2):c.479G>A (p.Arg160Lys)	GLTPD2, LOC130060033 (R196K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100381	NM_001014985.3(GLTPD2):c.506C>T (p.Ala169Val)	GLTPD2, LOC130060033 (A205V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251226	NM_001014985.3(GLTPD2):c.509C>T (p.Ala170Val)	GLTPD2, LOC130060033 (A170V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403332	NM_001014985.3(GLTPD2):c.538T>C (p.Ser180Pro)	GLTPD2, LOC130060033 (S180P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100382	NM_001014985.3(GLTPD2):c.541C>T (p.Arg181Cys)	GLTPD2, LOC130060033 (R181C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218895	NM_001014985.3(GLTPD2):c.560A>G (p.His187Arg)	GLTPD2, LOC130060033 (H187R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100383	NM_001014985.3(GLTPD2):c.595C>G (p.Arg199Gly)	GLTPD2, LOC130060033 (R199G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277209	NM_001014985.3(GLTPD2):c.598G>A (p.Val200Met)	GLTPD2, LOC130060033 (V236M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100384	NM_001014985.3(GLTPD2):c.642C>G (p.Cys214Trp)	GLTPD2, LOC130060033 (C214W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345658	NM_001014985.3(GLTPD2):c.652T>A (p.Tyr218Asn)	GLTPD2, LOC130060033 (Y218N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552229	NM_001014985.3(GLTPD2):c.659C>A (p.Ala220Glu)	GLTPD2, LOC130060033 (A220E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100385	NM_001014985.3(GLTPD2):c.668G>C (p.Gly223Ala)	GLTPD2, LOC130060033 (G223A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2356350	NM_001014985.3(GLTPD2):c.730C>T (p.Arg244Cys)	GLTPD2, LOC130060033 (R244C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484871	NM_001014985.3(GLTPD2):c.769G>C (p.Glu257Gln)	GLTPD2, LOC130060033 (E257Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2459228	NM_001014985.3(GLTPD2):c.851A>G (p.Glu284Gly)	GLTPD2, LOC130060033 (E284G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100386	NM_001014985.3(GLTPD2):c.853C>G (p.Arg285Gly)	GLTPD2, LOC130060033 (R321G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281660	NM_001014985.3(GLTPD2):c.856G>T (p.Gly286Cys)	GLTPD2, LOC130060033 (G322C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3243205	NC_000017.10:g.(?_422368)_(8285628_?)dup	FBXO39, FGF11 +209 more	Duplication	not provided	GUncertain significance
Select item 3063486	GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3	ABR, ACADVL +329 more	Copy number gain	not specified	GPathogenic
Select item 3063485	GRCh37/hg19 17p13.3-13.2(chr17:9474-6017500)x1	ABR, ALOX15 +116 more	Copy number loss	not specified	GPathogenic
Select item 1809320	GRCh37/hg19 17p13.2(chr17:4658216-5266343)x3	C17orf107, CAMTA2 +22 more	Copy number gain	not provided	GUncertain significance
Select item 1526561	GRCh37/hg19 17p13.2(chr17:4113551-5023913)	ALOX15, ANKFY1 +31 more	Copy number loss	not specified	GUncertain significance
Select item 816504	GRCh37/hg19 17p13.3-13.2(chr17:8547-5627408)x1	ABR, ALOX15 +115 more	Copy number loss	See cases	GPathogenic
Select item 688934	GRCh37/hg19 17p13.2(chr17:3759126-6128911)x1	ALOX15, ANKFY1 +48 more	Copy number loss	not provided	GUncertain significance
Select item 625578	GRCh37/hg19 17p13.3-13.2(chr17:47546-6287620)	ABR, ALOX15 +115 more	Copy number gain	Chromosome 17P13.3, telomeric, duplication syndrome	GPathogenic
Select item 564394	GRCh37/hg19 17p13.2(chr17:4633847-4926646)x3	INCA1, SLC25A11 +18 more	Copy number gain	not provided	GUncertain significance
Select item 564393	GRCh37/hg19 17p13.2(chr17:4475016-4884701)x3	ARRB2, MINK1 +20 more	Copy number gain	not provided	GUncertain significance
Select item 564392	GRCh37/hg19 17p13.2(chr17:4036861-5174346)x3	CXCL16, SLC52A1 +36 more	Copy number gain	not provided	GUncertain significance
Select item 564377	GRCh37/hg19 17p13.3-12(chr17:525-11186432)x3	ABR, ACADVL +240 more	Copy number gain	not provided	GPathogenic
Select item 443659	GRCh37/hg19 17p13.3-12(chr17:525-15027737)x3	ABR, ACADVL +250 more	Copy number gain	See cases	GPathogenic
Select item 441816	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	ALOX12, ALOX12B +1143 more	Copy number gain	See cases	GPathogenic
Select item 441815	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	SPEM2, TBCD +1143 more	Copy number gain	See cases	GPathogenic
Select item 441788	GRCh37/hg19 17p13.2(chr17:4633847-4856516)x1	C17orf107, CHRNE +14 more	Copy number loss	See cases	GUncertain significance
Select item 395716	GRCh37/hg19 17p13.3-13.1(chr17:1113102-6742486)	AIPL1, ALOX15 +115 more	Copy number gain	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: 60