RAB37[gene] - ClinVar

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Items: 64

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148363	GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3	AARSD1, AATF +2032 more	Copy number gain	See cases	GPathogenic
Select item 58703	GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3	MIR636, MIR6516 +1033 more	Copy number gain	See cases	GPathogenic
Select item 155275	GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3	AANAT, AATK +1013 more	Copy number gain	See cases	GPathogenic
Select item 59733	GRCh38/hg38 17q25.1(chr17:73851698-74732123)x3	BTBD17, CD300A +44 more	Copy number gain	See cases	GBenign
Select item 2271902	NM_139018.5(CD300LF):c.823G>A (p.Gly275Ser)	CD300LF, RAB37 (G275S +2 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GLikely benign
Select item 2492484	NM_139018.5(CD300LF):c.818T>C (p.Leu273Pro)	CD300LF, RAB37 (L276P +2 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2249530	NM_139018.5(CD300LF):c.746A>G (p.Tyr249Cys)	CD300LF, RAB37 (Y249C +2 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2216018	NM_139018.5(CD300LF):c.665C>T (p.Thr222Met)	CD300LF, RAB37 (T225M +2 more)	Single nucleotide variant (synonymous variant +3 more)	not specified	GUncertain significance
Select item 2233524	NM_139018.5(CD300LF):c.604G>A (p.Asp202Asn)	CD300LF, RAB37 (D202N +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2206337	NM_139018.5(CD300LF):c.460A>C (p.Lys154Gln)	CD300LF, RAB37 (K154Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140535	NM_139018.5(CD300LF):c.453G>C (p.Lys151Asn)	CD300LF, RAB37 (K169N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3140534	NM_139018.5(CD300LF):c.448C>T (p.His150Tyr)	CD300LF, RAB37 (A165V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140533	NM_139018.5(CD300LF):c.427G>A (p.Gly143Ser)	CD300LF, RAB37 (G158S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3140532	NM_139018.5(CD300LF):c.323G>A (p.Cys108Tyr)	CD300LF, RAB37 (C108Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3264814	NM_139018.5(CD300LF):c.291T>G (p.Asp97Glu)	CD300LF, RAB37 (D97E +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2648226	NM_139018.5(CD300LF):c.270G>T (p.Thr90=)	CD300LF, RAB37	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2210761	NM_139018.5(CD300LF):c.269C>T (p.Thr90Met)	CD300LF, RAB37 (T93M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2221572	NM_139018.5(CD300LF):c.236G>C (p.Arg79Pro)	CD300LF, RAB37 (R79P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2252081	NM_139018.5(CD300LF):c.172A>C (p.Ile58Leu)	CD300LF, RAB37 (I58L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2369134	NM_139018.5(CD300LF):c.164G>A (p.Arg55Gln)	CD300LF, RAB37 (R55Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2467699	NM_139018.5(CD300LF):c.131C>T (p.Ser44Leu)	CD300LF, RAB37 (S47L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2229128	NM_139018.5(CD300LF):c.110C>T (p.Thr37Ile)	CD300LF, RAB37 (T37I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140536	NM_139018.5(CD300LF):c.73C>T (p.Pro25Ser)	CD300LF, RAB37 (P25S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2214993	NM_001163989.3(RAB37):c.-87G>A	RAB37	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2322445	NM_001163989.3(RAB37):c.-86G>A	RAB37	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3150697	NM_001163989.3(RAB37):c.-84G>A	RAB37	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312142	NM_001163989.3(RAB37):c.-56C>T	RAB37	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2483580	NM_001163989.3(RAB37):c.-24G>A	RAB37	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3150694	NM_001006638.3(RAB37):c.97A>T (p.Met33Leu)	RAB37 (M1L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2545534	NM_001006638.3(RAB37):c.101T>C (p.Leu34Pro)	RAB37 (L34P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312140	NM_001006638.3(RAB37):c.173C>T (p.Thr58Ile)	RAB37 (T26I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2648227	NM_001006638.3(RAB37):c.186C>G (p.Thr62=)	RAB37	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2472994	NM_001006638.3(RAB37):c.229G>A (p.Val77Met)	RAB37 (V77M +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3312138	NM_001006638.3(RAB37):c.262G>A (p.Gly88Arg)	RAB37 (G88R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150696	NM_001006638.3(RAB37):c.272G>A (p.Arg91Gln)	RAB37 (R84Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620855	NM_001006638.3(RAB37):c.278G>A (p.Arg93Gln)	RAB37 (R56Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312141	NM_001006638.3(RAB37):c.319C>T (p.Leu107Phe)	RAB37 (L100F +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150698	NM_001006638.3(RAB37):c.355G>A (p.Asp119Asn)	RAB37 (D112N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512617	NM_001006638.3(RAB37):c.377C>A (p.Thr126Asn)	RAB37 (T119N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544468	NM_001006638.3(RAB37):c.398A>C (p.Gln133Pro)	RAB37 (Q133P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150699	NM_001006638.3(RAB37):c.407T>C (p.Val136Ala)	RAB37 (V109A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150700	NM_001006638.3(RAB37):c.434C>T (p.Ala145Val)	RAB37 (A118V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150701	NM_001006638.3(RAB37):c.441G>A (p.Met147Ile)	RAB37 (M115I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359991	NM_001006638.3(RAB37):c.448G>A (p.Glu150Lys)	RAB37 (E113K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511767	NM_001006638.3(RAB37):c.466G>A (p.Glu156Lys)	RAB37 (E156K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150702	NM_001006638.3(RAB37):c.488G>A (p.Arg163Lys)	RAB37 (R156K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222488	NM_001006638.3(RAB37):c.580C>T (p.Arg194Trp)	RAB37 (R162W +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470864	NM_001006638.3(RAB37):c.586G>A (p.Gly196Arg)	RAB37 (G164R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455678	NM_001006638.3(RAB37):c.590A>G (p.His197Arg)	RAB37 (H165R +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2592689	NM_001006638.3(RAB37):c.620G>A (p.Arg207Gln)	RAB37 (R200Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3150703	NM_001006638.3(RAB37):c.661T>G (p.Ser221Ala)	RAB37 (S194A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2578017	GRCh37/hg19 17q25.1(chr17:72718277-74142256)	ACOX1, ARMC7 +52 more	Copy number gain	7q11.23 microduplication syndrome	GPathogenic
Select item 1340830	GRCh37/hg19 17q25.1(chr17:71813960-72707349)x3	BTBD17, CD300A +13 more	Copy number gain	not provided	GLikely benign
Select item 815950	GRCh37/hg19 17q25.1(chr17:71811005-72681118)x3	BTBD17, CD300A +12 more	Copy number gain	not provided	GLikely benign
Select item 689209	GRCh37/hg19 17q24.1-25.3(chr17:62778720-81041938)x3	AANAT, AATK +226 more	Copy number gain	not provided	GPathogenic
Select item 625759	GRCh37/hg19 17q24.3-25.1(chr17:70720436-73175266)	BTBD17, ARMC7 +40 more	Copy number gain	not provided	GPathogenic
Select item 624519	GRCh37/hg19 17q24.1-25.2(chr17:64159738-74891024)x3	LLGL2, MAP2K6 +119 more	Copy number gain	not provided	GLikely pathogenic
Select item 564470	GRCh37/hg19 17q25.1(chr17:71810700-72702515)x3	BTBD17, CD300A +13 more	Copy number gain	not provided	GLikely benign
Select item 564463	GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3	AANAT, AATK +222 more	Copy number gain	not provided	GPathogenic
Select item 443488	GRCh37/hg19 17q24.2-25.3(chr17:67002415-81041938)x3	AANAT, AATK +202 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 395646	GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3	AANAT, AATK +458 more	Copy number gain	See cases	GPathogenic
Select item 393984	GRCh37/hg19 17q25.1(chr17:71940807-72667784)x3	BTBD17, CD300A +12 more	Copy number gain	See cases	GLikely benign

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Items: 64