Related gene-specific medical variations for Gene (Select 3200) - ClinVar

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Links from Gene

Items: 81

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3106595	NM_024014.4(HOXA6):c.616C>G (p.Arg206Gly)	HOXA-AS3, HOXA3 +1 more (R206G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106594	NM_024014.4(HOXA6):c.559G>A (p.Glu187Lys)	HOXA-AS3, HOXA3 +1 more (E187K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106593	NM_024014.4(HOXA6):c.395A>G (p.Tyr132Cys)	HOXA-AS3, HOXA3 +1 more (Y132C)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3106592	NM_024014.4(HOXA6):c.293G>A (p.Gly98Asp)	HOXA-AS3, HOXA3 +1 more (G98D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106590	NM_019102.4(HOXA5):c.340A>T (p.Ser114Cys)	HOXA-AS3, HOXA3 +1 more (S114C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106589	NM_019102.4(HOXA5):c.160C>G (p.Leu54Val)	HOXA-AS3, HOXA3 +1 more (L54V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106588	NM_002141.5(HOXA4):c.925C>A (p.His309Asn)	HOXA3, HOXA4 (H309N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106587	NM_002141.5(HOXA4):c.887A>G (p.Lys296Arg)	HOXA3, HOXA4 (K296R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106586	NM_002141.5(HOXA4):c.880C>A (p.Pro294Thr)	HOXA3, HOXA4 (P294T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106585	NM_002141.5(HOXA4):c.770G>A (p.Arg257His)	HOXA3, HOXA4 (R257H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106584	NM_002141.5(HOXA4):c.670C>T (p.Arg224Trp)	HOXA3, HOXA4 (R224W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106583	NM_002141.5(HOXA4):c.652T>C (p.Ser218Pro)	HOXA3, HOXA4 (S218P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106582	NM_002141.5(HOXA4):c.644C>G (p.Pro215Arg)	HOXA3, HOXA4 (P215R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106581	NM_002141.5(HOXA4):c.274G>C (p.Ala92Pro)	HOXA3, HOXA4 (A92P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106580	NM_002141.5(HOXA4):c.154C>T (p.His52Tyr)	HOXA3, HOXA4 (H52Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3054235	NM_002141.5(HOXA4):c.162G>A (p.Pro54=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	HOXA4-related disorder	GLikely benign
Select item 3053757	NM_002141.5(HOXA4):c.524G>A (p.Cys175Tyr)	HOXA3, HOXA4 (C175Y)	Single nucleotide variant (missense variant +1 more)	HOXA4-related disorder	GLikely benign
Select item 3052841	NM_002141.5(HOXA4):c.414C>G (p.Pro138=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	HOXA4-related disorder	GLikely benign
Select item 3052573	NM_002141.5(HOXA4):c.559C>G (p.Leu187Val)	HOXA3, HOXA4 (L187V)	Single nucleotide variant (missense variant +1 more)	HOXA4-related disorder	GLikely benign
Select item 3034411	NM_002141.5(HOXA4):c.243G>C (p.Glu81Asp)	HOXA3, HOXA4 (E81D)	Single nucleotide variant (missense variant +1 more)	HOXA4-related disorder	GLikely benign
Select item 3032651	NM_002141.5(HOXA4):c.285C>T (p.Ala95=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	HOXA4-related disorder	GLikely benign
Select item 2681318	NM_002141.5(HOXA4):c.727C>A (p.Arg243=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2681317	NM_002141.5(HOXA4):c.93C>T (p.Gly31=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2657364	NM_002141.5(HOXA4):c.102C>A (p.Gly34=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2657363	NM_002141.5(HOXA4):c.165G>T (p.Leu55=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2657362	NM_002141.5(HOXA4):c.319G>A (p.Gly107Ser)	HOXA3, HOXA4 (G107S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2619775	NM_019102.4(HOXA5):c.31G>C (p.Gly11Arg)	HOXA-AS3, HOXA3 +1 more (G11R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618771	NM_019102.4(HOXA5):c.6C>G (p.Ser2Arg)	HOXA-AS3, HOXA3 +1 more (S2R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607924	NM_002141.5(HOXA4):c.845G>C (p.Arg282Pro)	HOXA3, HOXA4 (R282P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607923	NM_002141.5(HOXA4):c.104G>A (p.Gly35Asp)	HOXA3, HOXA4 (G35D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598345	NM_002141.5(HOXA4):c.773A>G (p.Gln258Arg)	HOXA3, HOXA4 (Q258R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557867	NM_002141.5(HOXA4):c.268T>C (p.Tyr90His)	HOXA3, HOXA4 (Y90H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545210	NM_002141.5(HOXA4):c.280G>A (p.Gly94Arg)	HOXA3, HOXA4 (G94R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532101	NM_024014.4(HOXA6):c.652A>G (p.Asn218Asp)	HOXA-AS3, HOXA3 +1 more (N218D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530960	NM_002141.5(HOXA4):c.21G>T (p.Leu7Phe)	HOXA3, HOXA4 (L7F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526769	NM_002141.5(HOXA4):c.5C>T (p.Thr2Ile)	HOXA3, HOXA4 (T2I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515896	NM_019102.4(HOXA5):c.244G>C (p.Ala82Pro)	HOXA-AS3, HOXA3 +1 more (A82P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490565	NM_024014.4(HOXA6):c.670G>T (p.Gly224Trp)	HOXA-AS3, HOXA3 +1 more (G224W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489887	NM_002141.5(HOXA4):c.347C>T (p.Pro116Leu)	HOXA3, HOXA4 (P116L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406989	NM_002141.5(HOXA4):c.920A>G (p.His307Arg)	HOXA3, HOXA4 (H307R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402826	NM_019102.4(HOXA5):c.590G>C (p.Arg197Thr)	HOXA-AS3, HOXA3 +1 more (R197T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401908	NM_002141.5(HOXA4):c.46A>G (p.Lys16Glu)	HOXA3, HOXA4 (K16E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392560	NM_024014.4(HOXA6):c.491G>T (p.Arg164Leu)	HOXA-AS3, HOXA3 +1 more (R164L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380150	NM_024014.4(HOXA6):c.676G>A (p.Asp226Asn)	HOXA-AS3, HOXA3 +1 more (D226N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379689	NM_019102.4(HOXA5):c.478G>A (p.Ala160Thr)	HOXA-AS3, HOXA3 +1 more (A160T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378532	NM_019102.4(HOXA5):c.788C>T (p.Ala263Val)	HOXA-AS3, HOXA3 +1 more (A263V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363665	NM_002141.5(HOXA4):c.650G>A (p.Arg217His)	HOXA3, HOXA4 (R217H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362069	NM_002141.5(HOXA4):c.217T>C (p.Tyr73His)	HOXA3, HOXA4 (Y73H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355884	NM_002141.5(HOXA4):c.376C>G (p.Pro126Ala)	HOXA3, HOXA4 (P126A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354607	NM_024014.4(HOXA6):c.490C>T (p.Arg164Cys)	HOXA-AS3, HOXA3 +1 more (R164C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346797	NM_002141.5(HOXA4):c.133C>G (p.Pro45Ala)	HOXA3, HOXA4 (P45A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335986	NM_024014.4(HOXA6):c.402C>A (p.Ser134Arg)	HOXA-AS3, HOXA3 +1 more (S134R)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2332347	NM_024014.4(HOXA6):c.217G>C (p.Glu73Gln)	HOXA-AS3, HOXA3 +1 more (E73Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331912	NM_002141.5(HOXA4):c.362C>A (p.Ala121Glu)	HOXA3, HOXA4 (A121E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323430	NM_024014.4(HOXA6):c.110C>A (p.Pro37His)	HOXA-AS3, HOXA3 +1 more (P37H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2315380	NM_002141.5(HOXA4):c.215C>T (p.Ser72Phe)	HOXA3, HOXA4 (S72F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313365	NM_002141.5(HOXA4):c.425C>T (p.Pro142Leu)	HOXA3, HOXA4 (P142L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309313	NM_024014.4(HOXA6):c.502C>A (p.Leu168Met)	HOXA-AS3, HOXA3 +1 more (L168M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289764	NM_024014.4(HOXA6):c.656C>T (p.Ser219Phe)	HOXA-AS3, HOXA3 +1 more (S219F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286931	NM_002141.5(HOXA4):c.919C>T (p.His307Tyr)	HOXA3, HOXA4 (H307Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269018	NM_002141.5(HOXA4):c.823A>G (p.Lys275Glu)	HOXA3, HOXA4 (K275E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2264570	NM_002141.5(HOXA4):c.9G>T (p.Met3Ile)	HOXA3, HOXA4 (M3I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263198	NM_002141.5(HOXA4):c.100G>T (p.Gly34Cys)	HOXA3, HOXA4 (G34C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261982	NM_002141.5(HOXA4):c.374G>T (p.Gly125Val)	HOXA3, HOXA4 (G125V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250608	NM_024014.4(HOXA6):c.89C>A (p.Ala30Asp)	HOXA-AS3, HOXA3 +1 more (A30D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2247352	NM_002141.5(HOXA4):c.56C>T (p.Pro19Leu)	HOXA3, HOXA4 (P19L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235867	NM_002141.5(HOXA4):c.101G>C (p.Gly34Ala)	HOXA3, HOXA4 (G34A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224222	NM_002141.5(HOXA4):c.911T>G (p.Leu304Arg)	HOXA3, HOXA4 (L304R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223732	NM_002141.5(HOXA4):c.650G>T (p.Arg217Leu)	HOXA3, HOXA4 (R217L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1278464	NM_002141.5(HOXA4):c.*332G>C	HOXA3, HOXA4	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1270022	NM_002141.5(HOXA4):c.*254T>C	HOXA3, HOXA4	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 1269767	NM_002141.5(HOXA4):c.208A>C (p.Thr70Pro)	HOXA3, HOXA4 (T70P)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 1268576	NM_002141.5(HOXA4):c.616+120A>G	HOXA3, HOXA4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266176	NM_002141.5(HOXA4):c.617-198T>G	HOXA3, HOXA4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259086	NM_153631.3(HOXA3):c.-389-3894G>A	HOXA3, HOXA4 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256657	NM_002141.5(HOXA4):c.714A>C (p.Arg238=)	HOXA3, HOXA4	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1244153	NM_002141.5(HOXA4):c.617-179A>G	HOXA3, HOXA4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237183	NM_002141.5(HOXA4):c.194G>A (p.Gly65Asp)	HOXA3, HOXA4 (G65D)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1231880	NM_002141.5(HOXA4):c.419T>C (p.Leu140Pro)	HOXA3, HOXA4 (L140P)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1182927	NM_002141.5(HOXA4):c.*125G>A	HOXA4, HOXA3	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 774314	NM_019102.4(HOXA5):c.81T>C (p.His27=)	HOXA-AS3, HOXA3 +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign

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Links from Gene

Items: 81