"PreventionGenetics, part of Exact Sciences"[submitter] AND "DNAH17-AS - ClinVar

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Items: 49

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2234915	NM_173628.4(DNAH17):c.7558T>G (p.Phe2520Val)	DNAH17, DNAH17-AS1 (F2520V)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 3040525	NM_173628.4(DNAH17):c.7432C>T (p.Leu2478=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GLikely benign
Select item 402680	NM_173628.4(DNAH17):c.7422G>C (p.Thr2474=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition +2 more	GBenign
Select item 1294680	NM_173628.4(DNAH17):c.7295C>T (p.Thr2432Met)	DNAH17, DNAH17-AS1 (T2432M)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1282044	NM_173628.4(DNAH17):c.7276-27TCCCTCCCCT[3]	DNAH17, DNAH17-AS1	Microsatellite (intron variant)	not provided +1 more	GBenign
Select item 3042078	NM_173628.4(DNAH17):c.7041C>T (p.Tyr2347=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GBenign
Select item 3049087	NM_173628.4(DNAH17):c.7011C>T (p.Thr2337=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GLikely benign
Select item 402681	NM_173628.4(DNAH17):c.6975T>C (p.Ile2325=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition +2 more	GBenign
Select item 1266948	NM_173628.4(DNAH17):c.6972G>A (p.Thr2324=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition +1 more	GBenign
Select item 3032922	NM_173628.4(DNAH17):c.6818+1G>A	DNAH17, DNAH17-AS1	Single nucleotide variant (splice donor variant)	DNAH17-related condition	GLikely pathogenic
Select item 3044026	NM_173628.4(DNAH17):c.6801C>T (p.Ala2267=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GBenign
Select item 3034383	NM_173628.4(DNAH17):c.6729C>T (p.Phe2243=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GBenign
Select item 3048062	NM_173628.4(DNAH17):c.6669+4C>T	DNAH17, DNAH17-AS1	Single nucleotide variant (intron variant)	DNAH17-related condition	GLikely benign
Select item 2672712	NM_173628.4(DNAH17):c.6542-6C>T	DNAH17, DNAH17-AS1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 3056843	NM_173628.4(DNAH17):c.6492C>T (p.Cys2164=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GLikely benign
Select item 3041997	NM_173628.4(DNAH17):c.6469C>T (p.Leu2157=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GLikely benign
Select item 2648362	NM_173628.4(DNAH17):c.6462C>T (p.Ala2154=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition +1 more	GBenign
Select item 2648363	NM_173628.4(DNAH17):c.6420C>A (p.Ser2140=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition +1 more	GBenign/Likely benign
Select item 3038045	NM_173628.4(DNAH17):c.6251G>A (p.Arg2084Gln)	DNAH17, DNAH17-AS1 (R2084Q)	Single nucleotide variant (missense variant)	DNAH17-related condition	GBenign
Select item 3041473	NM_173628.4(DNAH17):c.6195C>T (p.Pro2065=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GLikely benign
Select item 3035385	NM_173628.4(DNAH17):c.6081G>A (p.Val2027=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GBenign
Select item 3045958	NM_173628.4(DNAH17):c.6051C>T (p.Tyr2017=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GBenign
Select item 402682	NM_173628.4(DNAH17):c.5956A>G (p.Met1986Val)	DNAH17, DNAH17-AS1 (M1986V)	Single nucleotide variant (missense variant)	DNAH17-related condition +2 more	GBenign
Select item 402683	NM_173628.4(DNAH17):c.5955C>G (p.Leu1985=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition +2 more	GBenign
Select item 3040118	NM_173628.4(DNAH17):c.5922C>T (p.Val1974=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GLikely benign
Select item 3037336	NM_173628.4(DNAH17):c.5862C>T (p.Ala1954=)	DNAH17, DNAH17-AS1	Single nucleotide variant (synonymous variant)	DNAH17-related condition	GBenign
Select item 3053933	NM_173628.4(DNAH17):c.5739C>T (p.Ala1913=)	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GLikely benign
Select item 3047841	NM_173628.4(DNAH17):c.5676G>A (p.Thr1892=)	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GLikely benign
Select item 3050531	NM_173628.4(DNAH17):c.5640+6C>T	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GLikely benign
Select item 2630533	NM_173628.4(DNAH17):c.5562_5563del (p.Glu1855fs)	DNAH17, DNAH17-AS1 (E1855fs)	Deletion (non-coding transcript variant +1 more)	DNAH17-related condition	GLikely pathogenic
Select item 3039523	NM_173628.4(DNAH17):c.5545G>A (p.Ala1849Thr)	DNAH17, DNAH17-AS1 (A1849T)	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GBenign
Select item 3053462	NM_173628.4(DNAH17):c.5544C>T (p.Pro1848=)	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GLikely benign
Select item 402685	NM_173628.4(DNAH17):c.5535T>C (p.Pro1845=)	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition +2 more	GBenign
Select item 3049210	NM_173628.4(DNAH17):c.5376C>T (p.Asp1792=)	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GLikely benign
Select item 2255496	NM_173628.4(DNAH17):c.5369G>A (p.Arg1790His)	DNAH17, DNAH17-AS1 (R1790H)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 3041515	NM_173628.4(DNAH17):c.5345C>T (p.Thr1782Ile)	DNAH17, DNAH17-AS1 (T1782I)	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GBenign
Select item 3038814	NM_173628.4(DNAH17):c.5323-9A>T	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GLikely benign
Select item 2648368	NM_173628.4(DNAH17):c.5322+8C>T	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition +1 more	GBenign/Likely benign
Select item 3039435	NM_173628.4(DNAH17):c.5314G>A (p.Val1772Met)	DNAH17, DNAH17-AS1 (V1772M)	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GBenign
Select item 3051349	NM_173628.4(DNAH17):c.5238C>T (p.Asn1746=)	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GLikely benign
Select item 402686	NM_173628.4(DNAH17):c.5226G>T (p.Met1742Ile)	DNAH17, DNAH17-AS1 (M1742I)	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition +2 more	GBenign
Select item 402704	NM_173628.4(DNAH17):c.5217G>A (p.Thr1739=)	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition +1 more	GLikely benign
Select item 768917	NM_173628.4(DNAH17):c.5216C>T (p.Thr1739Met)	DNAH17, DNAH17-AS1 (T1739M)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GBenign
Select item 3055422	NM_173628.4(DNAH17):c.5191-10T>C	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GBenign
Select item 402687	NM_173628.4(DNAH17):c.5171G>A (p.Arg1724Lys)	DNAH17-AS1, DNAH17 (R1724K)	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition +1 more	GBenign
Select item 3039803	NM_173628.4(DNAH17):c.5118C>T (p.Thr1706=)	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GLikely benign
Select item 3049520	NM_173628.4(DNAH17):c.5115G>A (p.Thr1705=)	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GBenign
Select item 3034340	NM_173628.4(DNAH17):c.5037C>T (p.Tyr1679=)	DNAH17, DNAH17-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition	GBenign
Select item 2473437	NM_173628.4(DNAH17):c.4976G>A (p.Arg1659Gln)	DNAH17, DNAH17-AS1 (R1659Q)	Single nucleotide variant (non-coding transcript variant +1 more)	DNAH17-related condition +1 more	GConflicting classifications of pathogenicity

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Items: 49