Related gene-specific medical variations for Gene (Select 101928809) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3316776	NM_018115.4(SDAD1):c.110A>G (p.His37Arg)	SDAD1, SDAD1-AS1 (H37R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316773	NM_018115.4(SDAD1):c.191C>T (p.Ala64Val)	SDAD1, SDAD1-AS1 (A64V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316771	NM_018115.4(SDAD1):c.263A>T (p.Asn88Ile)	SDAD1, SDAD1-AS1 (N88I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3158862	NM_018115.4(SDAD1):c.41C>T (p.Pro14Leu)	SDAD1, SDAD1-AS1 (P14L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3079190	NM_002416.3(CXCL9):c.341G>A (p.Arg114Gln)	CXCL9, SDAD1-AS1 (R114Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3079188	NM_002416.3(CXCL9):c.311A>C (p.Lys104Thr)	CXCL9, SDAD1-AS1 (K104T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606224	NM_002416.3(CXCL9):c.290A>C (p.Lys97Thr)	CXCL9, SDAD1-AS1 (K97T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604100	NM_002416.3(CXCL9):c.209G>C (p.Gly70Ala)	CXCL9, SDAD1-AS1 (G70A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547459	NM_002416.3(CXCL9):c.236C>T (p.Ser79Leu)	CXCL9, SDAD1-AS1 (S79L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525553	NM_018115.4(SDAD1):c.21C>G (p.Asn7Lys)	SDAD1, SDAD1-AS1 (N7K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313733	NM_018115.4(SDAD1):c.201T>G (p.Ser67Arg)	SDAD1, SDAD1-AS1 (S67R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2285774	NM_018115.4(SDAD1):c.106A>G (p.Asn36Asp)	SDAD1, SDAD1-AS1 (N36D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 729521	NM_018115.4(SDAD1):c.96A>G (p.Leu32=)	SDAD1, SDAD1-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 714479	NM_002416.3(CXCL9):c.375A>G (p.Thr125=)	CXCL9, SDAD1-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign