Related gene-specific medical variations for Gene (Select 196385) - ClinVar

Links from Gene

Items: 82

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3234299	NM_001372106.1(DNAH10):c.13026C>T (p.Leu4342=)	DNAH10OS, DNAH10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3083436	NM_001372106.1(DNAH10):c.13588A>T (p.Ile4530Phe)	DNAH10, DNAH10OS (I4412F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3083434	NM_001372106.1(DNAH10):c.13523T>C (p.Ile4508Thr)	DNAH10, DNAH10OS (I4508T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3083433	NM_001372106.1(DNAH10):c.13357C>G (p.Leu4453Val)	DNAH10, DNAH10OS (L4335V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083431	NM_001372106.1(DNAH10):c.13313C>T (p.Pro4438Leu)	DNAH10, DNAH10OS (P4320L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083430	NM_001372106.1(DNAH10):c.12952A>G (p.Ile4318Val)	DNAH10, DNAH10OS (I4318V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083429	NM_001372106.1(DNAH10):c.12950A>G (p.Tyr4317Cys)	DNAH10, DNAH10OS (Y4199C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3083428	NM_001372106.1(DNAH10):c.12541T>A (p.Tyr4181Asn)	DNAH10, DNAH10OS (Y4181N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3083427	NM_001372106.1(DNAH10):c.12428C>T (p.Ala4143Val)	DNAH10, DNAH10OS (A4025V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3083426	NM_001372106.1(DNAH10):c.12392C>T (p.Pro4131Leu)	DNAH10, DNAH10OS (P4013L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3083425	NM_001372106.1(DNAH10):c.12331C>A (p.Leu4111Met)	DNAH10, DNAH10OS (L3993M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3083420	NM_001372106.1(DNAH10):c.11497G>A (p.Gly3833Ser)	DNAH10, LOC126861667 (G3833S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3053277	NM_001372106.1(DNAH10):c.11232G>A (p.Glu3744=)	DNAH10, LOC126861667	Single nucleotide variant (synonymous variant)	DNAH10-related disorder	GLikely benign
Select item 3049440	NM_001372106.1(DNAH10):c.13395C>G (p.Gly4465=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	DNAH10-related disorder	GLikely benign
Select item 3043129	NM_001372106.1(DNAH10):c.11287C>A (p.Arg3763=)	DNAH10, LOC126861667	Single nucleotide variant (synonymous variant)	DNAH10-related disorder	GLikely benign
Select item 3039756	NM_001372106.1(DNAH10):c.13092G>T (p.Val4364=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	DNAH10-related disorder	GLikely benign
Select item 2643545	NM_001372106.1(DNAH10):c.13578G>A (p.Pro4526=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2643544	NM_001372106.1(DNAH10):c.13303G>A (p.Glu4435Lys)	DNAH10, DNAH10OS (E4317K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2643543	NM_001372106.1(DNAH10):c.13281C>T (p.Ser4427=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643542	NM_001372106.1(DNAH10):c.12813C>G (p.Asn4271Lys)	DNAH10, DNAH10OS (N4153K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2643541	NM_001372106.1(DNAH10):c.12288T>A (p.Ile4096=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2643540	NM_001372106.1(DNAH10):c.12270G>A (p.Lys4090=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2643539	NM_001372106.1(DNAH10):c.12106-6G>A	DNAH10, DNAH10OS	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2643538	NM_001372106.1(DNAH10):c.11394A>G (p.Leu3798=)	DNAH10, LOC126861667	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2547109	NM_001372106.1(DNAH10):c.12649C>T (p.Arg4217Cys)	DNAH10, DNAH10OS (R4217C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547008	NM_001372106.1(DNAH10):c.11282G>A (p.Arg3761Lys)	DNAH10, LOC126861667 (R3643K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516645	NM_001372106.1(DNAH10):c.13361C>T (p.Thr4454Met)	DNAH10, DNAH10OS (T4454M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513405	NM_001372106.1(DNAH10):c.12674A>C (p.Asp4225Ala)	DNAH10, DNAH10OS (D4107A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509828	NM_001372106.1(DNAH10):c.12209T>C (p.Leu4070Pro)	DNAH10, DNAH10OS (L4070P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509781	NM_001372106.1(DNAH10):c.13307G>C (p.Ser4436Thr)	DNAH10, DNAH10OS (S4318T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2504194	NM_001372106.1(DNAH10):c.12605T>C (p.Ile4202Thr)	DNAH10, DNAH10OS (I4084T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2486396	NM_001372106.1(DNAH10):c.12172C>T (p.Leu4058Phe)	DNAH10, DNAH10OS (L4058F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478161	NM_001372106.1(DNAH10):c.12421G>A (p.Val4141Met)	DNAH10, DNAH10OS (V4141M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465643	NM_001372106.1(DNAH10):c.13469C>T (p.Ala4490Val)	DNAH10, DNAH10OS (A4490V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408356	NM_001372106.1(DNAH10):c.13096C>T (p.Arg4366Trp)	DNAH10, DNAH10OS (R4248W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405968	NM_001372106.1(DNAH10):c.13334G>A (p.Gly4445Glu)	DNAH10, DNAH10OS (G4445E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405486	NM_001372106.1(DNAH10):c.13046C>A (p.Thr4349Asn)	DNAH10, DNAH10OS (T4231N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404712	NM_001372106.1(DNAH10):c.12844G>A (p.Ala4282Thr)	DNAH10, DNAH10OS (A4164T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402175	NM_001372106.1(DNAH10):c.13293G>T (p.Leu4431Phe)	DNAH10, DNAH10OS (L4313F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401430	NM_001372106.1(DNAH10):c.13466G>A (p.Arg4489Gln)	DNAH10, DNAH10OS (R4489Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391623	NM_001372106.1(DNAH10):c.12809C>G (p.Ala4270Gly)	DNAH10, DNAH10OS (A4152G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364216	NM_001372106.1(DNAH10):c.13393G>A (p.Gly4465Ser)	DNAH10, DNAH10OS (G4465S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309791	NM_001372106.1(DNAH10):c.12882G>A (p.Met4294Ile)	DNAH10, DNAH10OS (M4176I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304860	NM_001372106.1(DNAH10):c.12427G>A (p.Ala4143Thr)	DNAH10, DNAH10OS (A4143T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286920	NM_001372106.1(DNAH10):c.12796G>A (p.Ala4266Thr)	DNAH10, DNAH10OS (A4148T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271618	NM_001372106.1(DNAH10):c.13218G>C (p.Arg4406Ser)	DNAH10, DNAH10OS (R4288S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266918	NM_001372106.1(DNAH10):c.11363C>T (p.Ser3788Phe)	DNAH10, LOC126861667 (S3788F +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2263899	NM_001372106.1(DNAH10):c.12668A>G (p.Tyr4223Cys)	DNAH10, DNAH10OS (Y4105C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257453	NM_001372106.1(DNAH10):c.12637G>A (p.Asp4213Asn)	DNAH10, DNAH10OS (D4095N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248909	NM_001372106.1(DNAH10):c.11440C>G (p.Leu3814Val)	DNAH10, LOC126861667 (L3696V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246193	NM_001372106.1(DNAH10):c.13219C>T (p.Leu4407Phe)	DNAH10, DNAH10OS (L4407F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238482	NM_001372106.1(DNAH10):c.12956G>C (p.Gly4319Ala)	DNAH10, DNAH10OS (G4201A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232857	NM_001372106.1(DNAH10):c.13274G>A (p.Arg4425Gln)	DNAH10, DNAH10OS (R4307Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225170	NM_001372106.1(DNAH10):c.12793G>A (p.Glu4265Lys)	DNAH10, DNAH10OS (E4147K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221599	NM_001372106.1(DNAH10):c.11423C>T (p.Ser3808Leu)	DNAH10, LOC126861667 (S3690L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215870	NM_001372106.1(DNAH10):c.11245C>T (p.Leu3749Phe)	DNAH10, LOC126861667 (L3631F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211744	NM_001372106.1(DNAH10):c.12257C>T (p.Thr4086Met)	DNAH10, DNAH10OS (T3968M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207856	NM_001372106.1(DNAH10):c.12526G>A (p.Glu4176Lys)	DNAH10, DNAH10OS (E4176K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204916	NM_001372106.1(DNAH10):c.13409G>A (p.Arg4470His)	DNAH10, DNAH10OS (R4352H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1700841	NM_001372106.1(DNAH10):c.11321C>T (p.Ala3774Val)	DNAH10, LOC126861667 (A3656V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1526397	NM_001372106.1(DNAH10):c.12241C>T (p.Arg4081Cys)	DNAH10, DNAH10OS (R3963C +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 56	GUncertain significance
Select item 1331109	NM_001372106.1(DNAH10):c.12124G>C (p.Glu4042Gln)	DNAH10, DNAH10OS (E3924Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1217310	NM_001372106.1(DNAH10):c.13192G>A (p.Gly4398Arg)	DNAH10, DNAH10OS (G4280R +1 more)	Single nucleotide variant (missense variant)	Spermatogenic failure 56	GLikely pathogenic
Select item 1217308	NM_001372106.1(DNAH10):c.12589del (p.Ser4197fs)	DNAH10, DNAH10OS (S4079fs +1 more)	Deletion (frameshift variant)	Spermatogenic failure 56	GPathogenic
Select item 978008	NM_001372106.1(DNAH10):c.3575A>G (p.Asn1192Ser)	DNAH10 (N1074S +1 more)	Single nucleotide variant (missense variant)	Male infertility	GUncertain significance
Select item 978007	NM_001372106.1(DNAH10):c.3868C>T (p.Leu1290Phe)	DNAH10 (L1172F +1 more)	Single nucleotide variant (missense variant)	Male infertility	GUncertain significance
Select item 978006	NM_001372106.1(DNAH10):c.11308G>A (p.Ala3770Thr)	DNAH10, LOC126861667 (A3652T +1 more)	Single nucleotide variant (missense variant)	Male infertility	GUncertain significance
Select item 978004	NM_001372106.1(DNAH10):c.10528C>G (p.Pro3510Ala)	DNAH10 (P3392A +1 more)	Single nucleotide variant (missense variant)	Male infertility	GUncertain significance
Select item 806964	NM_001372106.1(DNAH10):c.12128C>T (p.Thr4043Met)	DNAH10, DNAH10OS (T3925M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 787938	NM_001372106.1(DNAH10):c.12411G>A (p.Pro4137=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 781818	NM_001372106.1(DNAH10):c.11213C>T (p.Thr3738Ile)	DNAH10, LOC126861667 (T3620I +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 779616	NM_001372106.1(DNAH10):c.12564A>G (p.Gln4188=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 773690	NM_001372106.1(DNAH10):c.13408C>T (p.Arg4470Cys)	DNAH10, DNAH10OS (R4352C +1 more)	Single nucleotide variant (missense variant)	DNAH10-related disorder +1 more	GBenign
Select item 773030	NM_001372106.1(DNAH10):c.11506+3G>A	DNAH10, LOC126861667	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 740996	NM_001372106.1(DNAH10):c.13291T>C (p.Leu4431=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 727119	NM_001372106.1(DNAH10):c.12916+8_12916+9del	DNAH10, DNAH10OS	Microsatellite (intron variant)	not provided	GLikely benign
Select item 726915	NM_001372106.1(DNAH10):c.13032A>C (p.Thr4344=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 726552	NM_001372106.1(DNAH10):c.12780T>C (p.Phe4260=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 712127	NM_001372106.1(DNAH10):c.12132G>A (p.Ala4044=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 711074	NM_001372106.1(DNAH10):c.12281T>C (p.Ile4094Thr)	DNAH10, DNAH10OS (I3976T +1 more)	Single nucleotide variant (missense variant)	DNAH10-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 402626	NM_001372106.1(DNAH10):c.13392C>T (p.Asn4464=)	DNAH10, DNAH10OS	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 402625	NM_001372106.1(DNAH10):c.13308C>T (p.Ser4436=)	DNAH10OS, DNAH10	Single nucleotide variant (synonymous variant)	DNAH10-related disorder +1 more	GBenign

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Items: 82