Related gene-specific medical variations for Gene (Select 221935) - ClinVar

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Links from Gene

Items: 75

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3316954	NM_152744.4(SDK1):c.4217G>A (p.Gly1406Asp)	LOC105375131, SDK1 (G1406D)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3316939	NM_152744.4(SDK1):c.1627G>A (p.Val543Ile)	LOC126859931, SDK1 (V543I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316931	NM_152744.4(SDK1):c.1592T>C (p.Met531Thr)	LOC126859931, SDK1 (M531T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158996	NM_152744.4(SDK1):c.8G>C (p.Arg3Pro)	SDK1, SDK1-AS1 (R3P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158962	NM_152744.4(SDK1):c.4162G>A (p.Glu1388Lys)	LOC105375131, SDK1 (E1388K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3158961	NM_152744.4(SDK1):c.4130C>T (p.Ala1377Val)	LOC105375131, SDK1 (A1377V)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3158960	NM_152744.4(SDK1):c.4125C>T (p.Asp1375=)	LOC105375131, SDK1	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign
Select item 3158944	NM_152744.4(SDK1):c.254C>T (p.Ala85Val)	SDK1, SDK1-AS1 (A85V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158942	NM_152744.4(SDK1):c.225G>C (p.Lys75Asn)	SDK1, SDK1-AS1 (K75N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2685232	GRCh37/hg19 7p22.2(chr7:4084716-4221000)x1	SDK1	Copy number loss	not provided	GUncertain significance
Select item 2685231	GRCh37/hg19 7p22.2(chr7:3806198-3929141)x1	SDK1	Copy number loss	not provided	GUncertain significance
Select item 2684478	GRCh37/hg19 7p22.2(chr7:3276126-4017614)x3	SDK1	Copy number gain	not provided	GUncertain significance
Select item 2657245	NM_152744.4(SDK1):c.243C>G (p.Arg81=)	SDK1, SDK1-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2621242	NM_152744.4(SDK1):c.92C>A (p.Ser31Tyr)	SDK1, SDK1-AS1 (S31Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620612	NM_152744.4(SDK1):c.92C>T (p.Ser31Phe)	SDK1, SDK1-AS1 (S31F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612573	NM_152744.4(SDK1):c.4039G>A (p.Val1347Met)	LOC105375131, SDK1 (V1347M)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2610323	NM_152744.4(SDK1):c.155G>C (p.Arg52Pro)	SDK1, SDK1-AS1 (R52P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597777	NM_152744.4(SDK1):c.1697C>T (p.Ala566Val)	LOC126859931, SDK1 (A566V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594989	NM_152744.4(SDK1):c.287C>T (p.Ala96Val)	SDK1, SDK1-AS1 (A96V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592895	NM_152744.4(SDK1):c.16C>T (p.Arg6Trp)	SDK1, SDK1-AS1 (R6W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560052	NM_152744.4(SDK1):c.1547A>T (p.Glu516Val)	LOC126859931, SDK1 (E516V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549052	NM_152744.4(SDK1):c.3988G>A (p.Val1330Met)	LOC105375131, SDK1 (V1330M)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2527760	NM_152744.4(SDK1):c.4175C>T (p.Thr1392Ile)	LOC105375131, SDK1 (T1392I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2457450	NM_152744.4(SDK1):c.86G>A (p.Arg29Gln)	SDK1, SDK1-AS1 (R29Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407200	NM_152744.4(SDK1):c.202T>G (p.Cys68Gly)	SDK1, SDK1-AS1 (C68G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384864	NM_152744.4(SDK1):c.263C>G (p.Ala88Gly)	SDK1, SDK1-AS1 (A88G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358558	NM_152744.4(SDK1):c.168G>T (p.Glu56Asp)	SDK1, SDK1-AS1 (E56D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352814	NM_152744.4(SDK1):c.140A>C (p.Glu47Ala)	SDK1, SDK1-AS1 (E47A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343065	NM_152744.4(SDK1):c.142C>A (p.Pro48Thr)	SDK1, SDK1-AS1 (P48T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342528	NM_152744.4(SDK1):c.58C>G (p.Pro20Ala)	SDK1, SDK1-AS1 (P20A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2331808	NM_152744.4(SDK1):c.1582C>T (p.Pro528Ser)	LOC126859931, SDK1 (P528S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321339	NM_152744.4(SDK1):c.232C>A (p.Pro78Thr)	SDK1, SDK1-AS1 (P78T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313065	NM_152744.4(SDK1):c.4153G>T (p.Val1385Leu)	LOC105375131, SDK1 (V1385L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2275401	NM_152744.4(SDK1):c.1562C>A (p.Ala521Asp)	LOC126859931, SDK1 (A521D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260007	NM_152744.4(SDK1):c.211C>T (p.Arg71Trp)	SDK1, SDK1-AS1 (R71W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251703	NM_152744.4(SDK1):c.167A>C (p.Glu56Ala)	SDK1, SDK1-AS1 (E56A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244063	NM_152744.4(SDK1):c.169A>C (p.Thr57Pro)	SDK1, SDK1-AS1 (T57P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239124	NM_152744.4(SDK1):c.206G>T (p.Gly69Val)	SDK1, SDK1-AS1 (G69V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206346	NM_152744.4(SDK1):c.182A>C (p.Asp61Ala)	SDK1, SDK1-AS1 (D61A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808348	GRCh37/hg19 7p22.2(chr7:3624238-3896871)x3	SDK1	Copy number gain	not provided	GUncertain significance
Select item 1527333	GRCh37/hg19 7p22.2(chr7:3946176-4023801)	SDK1	Copy number loss	not specified	GUncertain significance
Select item 1341002	GRCh37/hg19 7p22.2(chr7:3251557-3685015)x3	SDK1	Copy number gain	not provided	GLikely benign
Select item 1340881	GRCh37/hg19 7p22.2(chr7:3648164-3816744)x1	SDK1	Copy number loss	not provided	GLikely benign
Select item 980812	GRCh37/hg19 7p22.2(chr7:3344114-3559769)x3	SDK1	Copy number gain	not provided	GUncertain significance
Select item 980811	GRCh37/hg19 7p22.2(chr7:3617996-3757295)x1	SDK1	Copy number loss	not provided	GLikely benign
Select item 980264	GRCh37/hg19 7p22.2(chr7:4202337-4322838)x1	SDK1	Copy number loss	not provided	GLikely benign
Select item 974753	NC_000007.13:g.3627221_3759274del	SDK1	Deletion	Megacolon	GUncertain significance
Select item 814920	GRCh37/hg19 7p22.2(chr7:3834690-3889956)x1	SDK1	Copy number loss	not provided	GUncertain significance
Select item 814919	GRCh37/hg19 7p22.2-22.1(chr7:3787297-4646250)x3	SDK1	Copy number gain	not provided	GLikely benign
Select item 814918	GRCh37/hg19 7p22.2(chr7:3624237-4407905)x3	SDK1	Copy number gain	not provided	GLikely benign
Select item 814917	GRCh37/hg19 7p22.2(chr7:3377925-3716852)x3	SDK1	Copy number gain	not provided	GLikely benign
Select item 780670	NM_152744.4(SDK1):c.4041G>A (p.Val1347=)	LOC105375131, SDK1	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GBenign
Select item 689199	GRCh37/hg19 7p22.2-22.1(chr7:3813870-4673949)x3	SDK1	Copy number gain	not provided	GUncertain significance
Select item 688967	GRCh37/hg19 7p22.2(chr7:4257728-4341965)x1	SDK1	Copy number loss	not provided	GUncertain significance
Select item 688940	GRCh37/hg19 7p22.2(chr7:3787297-3943481)x1	SDK1	Copy number loss	not provided	GUncertain significance
Select item 687312	GRCh37/hg19 7p22.2(chr7:4151644-4421645)x3	SDK1	Copy number gain	not provided	GUncertain significance
Select item 687275	GRCh37/hg19 7p22.2(chr7:3849467-3917280)x1	SDK1	Copy number loss	not provided	GUncertain significance
Select item 686627	GRCh37/hg19 7p22.2(chr7:4289287-4404049)x3	SDK1	Copy number gain	not provided	GUncertain significance
Select item 624515	GRCh37/hg19 7p22.2(chr7:4289827-4421032)x3	SDK1	Copy number gain	not provided	GUncertain significance
Select item 563380	GRCh37/hg19 7p22.2-22.1(chr7:3813870-4685115)x3	SDK1	Copy number gain	not provided	GLikely benign
Select item 563319	GRCh37/hg19 7p22.2(chr7:3526696-3745015)x1	SDK1	Copy number loss	not provided	GUncertain significance
Select item 563286	GRCh37/hg19 7p22.2(chr7:3949727-4025972)x1	SDK1	Copy number loss	not provided	GUncertain significance
Select item 445721	NM_152744.4(SDK1):c.1255C>G (p.Gln419Glu)	SDK1 (Q419E)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 444712	NM_152744.4(SDK1):c.5277C>T (p.Pro1759=)	SDK1	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 444711	NM_152744.4(SDK1):c.3520G>A (p.Asp1174Asn)	SDK1 (D1174N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 444710	NM_152744.4(SDK1):c.1608_1610del (p.Gly537del)	LOC126859931, SDK1 (G537del)	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 443036	GRCh37/hg19 7p22.2-22.1(chr7:3813870-4674445)x3	SDK1	Copy number gain	See cases	GLikely benign
Select item 441768	GRCh37/hg19 7p22.2(chr7:3086310-3703105)x3	SDK1	Copy number gain	See cases	GLikely benign
Select item 441062	GRCh37/hg19 7p22.2(chr7:3543270-4045261)x3	SDK1	Copy number gain	not provided	Gnot provided
Select item 254004	GRCh37/hg19 7p22.2(chr7:3347012-3942058)x1	SDK1	Copy number loss	See cases	GUncertain significance
Select item 161816	NM_152744.4(SDK1):c.5214+8C>T	SDK1	Single nucleotide variant (intron variant)	Malignant tumor of prostate	GUncertain significance
Select item 157035	NM_152744.3(SDK1):c.299-49000_299-30913del	SDK1	Deletion	Normal pregnancy	Gnot provided
Select item 154497	GRCh38/hg38 7p22.2(chr7:3589872-3697219)x1	SDK1	Copy number loss	See cases	GLikely benign
Select item 153867	GRCh38/hg38 7p22.2(chr7:3387420-3667729)x1	SDK1	Copy number loss	See cases	GUncertain significance
Select item 149829	GRCh38/hg38 7p22.2(chr7:3383575-3657796)x3	SDK1	Copy number gain	See cases	GLikely benign

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Links from Gene

Items: 75