"Ambry Genetics"[submitter] AND "LMCD1"[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3119256	NM_014583.4(LMCD1):c.63G>T (p.Gln21His)	LMCD1 (Q21H)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3119257	NM_014583.4(LMCD1):c.71G>C (p.Arg24Thr)	LMCD1 (R24T)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2235689	NM_014583.4(LMCD1):c.100A>G (p.Thr34Ala)	LMCD1 (T34A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385566	NM_014583.4(LMCD1):c.199C>T (p.Arg67Trp)	LMCD1 (R67W)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2213071	NM_014583.4(LMCD1):c.209G>C (p.Gly70Ala)	LMCD1 (G70A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3119252	NM_014583.4(LMCD1):c.250C>T (p.Arg84Trp)	LMCD1 (R84W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535630	NM_014583.4(LMCD1):c.274C>T (p.Arg92Trp)	LMCD1 (R92W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537185	NM_014583.4(LMCD1):c.292C>T (p.Arg98Trp)	LMCD1 (R25W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608428	NM_014583.4(LMCD1):c.392T>C (p.Leu131Pro)	LMCD1 (L131P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225774	NM_014583.4(LMCD1):c.426G>T (p.Gln142His)	LMCD1 (Q30H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332787	NM_014583.4(LMCD1):c.439A>C (p.Thr147Pro)	LMCD1 (T147P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119253	NM_014583.4(LMCD1):c.440C>T (p.Thr147Ile)	LMCD1 (T74I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119254	NM_014583.4(LMCD1):c.460C>T (p.Arg154Cys)	LMCD1 (R154C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541396	NM_014583.4(LMCD1):c.514C>T (p.Arg172Cys)	LMCD1 (R60C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551045	NM_014583.4(LMCD1):c.515G>C (p.Arg172Pro)	LMCD1 (R99P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511189	NM_014583.4(LMCD1):c.515G>A (p.Arg172His)	LMCD1 (R60H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477341	NM_014583.4(LMCD1):c.542T>A (p.Leu181Gln)	LMCD1 (L181Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119255	NM_014583.4(LMCD1):c.574G>A (p.Glu192Lys)	LMCD1 (E80K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355107	NM_014583.4(LMCD1):c.605C>T (p.Pro202Leu)	LMCD1 (P129L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222912	NM_014583.4(LMCD1):c.616G>T (p.Gly206Cys)	LMCD1 (G206C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119258	NM_014583.4(LMCD1):c.743G>A (p.Gly248Glu)	LMCD1 (G136E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245396	NM_014583.4(LMCD1):c.763C>T (p.Pro255Ser)	LMCD1 (P143S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490301	NM_014583.4(LMCD1):c.878C>T (p.Ala293Val)	LMCD1 (A220V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283820	NM_014583.4(LMCD1):c.916C>T (p.Pro306Ser)	LMCD1 (P233S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119259	NM_014583.4(LMCD1):c.934G>A (p.Asp312Asn)	LMCD1 (D200N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208250	NM_014583.4(LMCD1):c.949G>A (p.Ala317Thr)	LMCD1 (A205T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487538	NM_014583.4(LMCD1):c.950C>T (p.Ala317Val)	LMCD1 (A205V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362627	NM_014583.4(LMCD1):c.965G>A (p.Arg322His)	LMCD1 (R210H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459994	NM_014583.4(LMCD1):c.1005T>G (p.Cys335Trp)	LMCD1 (C335W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119251	NM_014583.4(LMCD1):c.1040A>G (p.Tyr347Cys)	LMCD1 (Y347C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223353	NM_014583.4(LMCD1):c.1045G>A (p.Val349Ile)	LMCD1 (V237I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31