Related gene-specific medical variations for Gene (Select 100507064) - ClinVar

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Links from Gene

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3294083	NM_032849.4(MEDAG):c.226G>T (p.Gly76Cys)	MEDAG, TEX26-AS1 (G76C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294081	NM_032849.4(MEDAG):c.811T>C (p.Cys271Arg)	MEDAG, TEX26-AS1 (C271R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125101	NM_032849.4(MEDAG):c.686C>T (p.Pro229Leu)	MEDAG, TEX26-AS1 (P229L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125100	NM_032849.4(MEDAG):c.640G>A (p.Val214Ile)	MEDAG, TEX26-AS1 (V214I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3125099	NM_032849.4(MEDAG):c.622T>C (p.Phe208Leu)	MEDAG, TEX26-AS1 (F208L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125098	NM_032849.4(MEDAG):c.401C>T (p.Ala134Val)	MEDAG, TEX26-AS1 (A134V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125096	NM_032849.4(MEDAG):c.400G>A (p.Ala134Thr)	MEDAG, TEX26-AS1 (A134T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125095	NM_032849.4(MEDAG):c.395C>A (p.Thr132Lys)	MEDAG, TEX26-AS1 (T132K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125094	NM_032849.4(MEDAG):c.38G>A (p.Ser13Asn)	MEDAG, TEX26-AS1 (S13N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125093	NM_032849.4(MEDAG):c.304G>T (p.Asp102Tyr)	MEDAG, TEX26-AS1 (D102Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125092	NM_032849.4(MEDAG):c.225C>A (p.Asp75Glu)	MEDAG, TEX26-AS1 (D75E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125091	NM_032849.4(MEDAG):c.191C>G (p.Ala64Gly)	MEDAG, TEX26-AS1 (A64G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2643712	NM_032849.4(MEDAG):c.396G>A (p.Thr132=)	MEDAG, TEX26-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2602840	NM_032849.4(MEDAG):c.244G>A (p.Gly82Arg)	MEDAG, TEX26-AS1 (G82R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569955	NM_032849.4(MEDAG):c.577G>T (p.Ala193Ser)	MEDAG, TEX26-AS1 (A193S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515072	NM_032849.4(MEDAG):c.233T>A (p.Val78Glu)	TEX26-AS1, MEDAG (V78E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385503	NM_032849.4(MEDAG):c.73C>A (p.Leu25Met)	MEDAG, TEX26-AS1 (L25M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370667	NM_032849.4(MEDAG):c.750C>A (p.Ser250Arg)	MEDAG, TEX26-AS1 (S250R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292450	NM_032849.4(MEDAG):c.413A>T (p.Asn138Ile)	MEDAG, TEX26-AS1 (N138I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257539	NM_032849.4(MEDAG):c.479T>C (p.Ile160Thr)	MEDAG, TEX26-AS1 (I160T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226170	NM_032849.4(MEDAG):c.650T>C (p.Val217Ala)	MEDAG, TEX26-AS1 (V217A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223503	NM_032849.4(MEDAG):c.733C>G (p.Pro245Ala)	MEDAG, TEX26-AS1 (P245A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 22