Related gene-specific medical variations for Gene (Select 105375132) - ClinVar

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Links from Gene

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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 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 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 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

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Links from Gene

Items: 22