Dand5 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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20 records found for search term Dand5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
596948098	CV3547693	microsatellite	NM_152654.3(DAND5):c.-36ACAG[2]	not provided [RCV004811998]	benign	19	12969624	12969627	Human		name
155267576	CV1697495	deletion	NM_152654.3(DAND5):c.197del (p.Leu66fs)	Heterotaxy [RCV002281634]\|Heterotaxy, visceral, 13, autosomal [RCV005051954]	pathogenic\|uncertain significance	19	12969857	12969857	Human	4	name
405679792	CV3236735	single nucleotide variant	NM_152654.3(DAND5):c.47C>T (p.Ala16Val)	not specified [RCV004370886]	uncertain significance	19	12969707	12969707	Human		name
597674628	CV3655196	single nucleotide variant	NM_152654.3(DAND5):c.97T>C (p.Ser33Pro)	not specified [RCV004913631]	likely benign	19	12969757	12969757	Human		name
597674654	CV3655198	single nucleotide variant	NM_152654.3(DAND5):c.68G>C (p.Arg23Thr)	not specified [RCV004913633]	uncertain significance	19	12969728	12969728	Human		name
598251439	CV3963370	single nucleotide variant	NM_152654.3(DAND5):c.89G>A (p.Arg30Gln)	not specified [RCV005323062]	uncertain significance	19	12969749	12969749	Human		name
155906221	CV2303274	single nucleotide variant	NM_152654.3(DAND5):c.284A>G (p.Glu95Gly)	not specified [RCV004159024]	uncertain significance	19	12969944	12969944	Human		name
155975154	CV2342634	single nucleotide variant	NM_152654.3(DAND5):c.235C>T (p.Arg79Cys)	not specified [RCV004196720]	uncertain significance	19	12969895	12969895	Human		name
407452955	CV3430091	single nucleotide variant	NM_152654.3(DAND5):c.217G>T (p.Gly73Trp)	not specified [RCV004608759]	uncertain significance	19	12969877	12969877	Human		name
407452959	CV3430093	single nucleotide variant	NM_152654.3(DAND5):c.256G>T (p.Ala86Ser)	not specified [RCV004608761]	uncertain significance	19	12969916	12969916	Human		name
156325031	CV2335146	single nucleotide variant	NM_152654.3(DAND5):c.313C>T (p.Pro105Ser)	not specified [RCV004184676]	uncertain significance	19	12969973	12969973	Human		name
156125163	CV2350168	single nucleotide variant	NM_152654.3(DAND5):c.532A>G (p.Met178Val)	not specified [RCV004200083]	likely benign	19	12973596	12973596	Human		name
329375067	CV2439965	single nucleotide variant	NM_152654.3(DAND5):c.461G>A (p.Arg154His)	not specified [RCV004260446]	likely benign	19	12973525	12973525	Human		name
405679787	CV3236734	single nucleotide variant	NM_152654.3(DAND5):c.407G>T (p.Gly136Val)	not specified [RCV004370885]	uncertain significance	19	12973471	12973471	Human		name
407452961	CV3430094	single nucleotide variant	NM_152654.3(DAND5):c.346T>G (p.Ser116Ala)	not specified [RCV004608762]	uncertain significance	19	12973410	12973410	Human		name
597674604	CV3655194	single nucleotide variant	NM_152654.3(DAND5):c.334C>T (p.Arg112Trp)	not specified [RCV004913629]	uncertain significance	19	12973398	12973398	Human		name
597674617	CV3655195	single nucleotide variant	NM_152654.3(DAND5):c.355C>T (p.Arg119Cys)	not specified [RCV004913630]	uncertain significance	19	12973419	12973419	Human		name
597674641	CV3655197	single nucleotide variant	NM_152654.3(DAND5):c.419C>T (p.Thr140Ile)	not specified [RCV004913632]	uncertain significance	19	12973483	12973483	Human		name
598251450	CV3963372	single nucleotide variant	NM_152654.3(DAND5):c.431T>C (p.Leu144Pro)	not specified [RCV005323064]	uncertain significance	19	12973495	12973495	Human		name
150520478	CV1053659	microsatellite	NM_152654.3(DAND5):c.396_397dup (p.Tyr133fs)	Heterotaxy [RCV001732154]\|not provided [RCV001822873]	pathogenic\|likely pathogenic\|uncertain significance	19	12973453	12973454	Human		name

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