Related gene-specific medical variations for Gene (Select 56670) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3323523	NM_033050.6(SUCNR1):c.296G>A (p.Arg99Gln)	AADACL2-AS1, SUCNR1 (R99Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3323522	NM_033050.6(SUCNR1):c.814G>A (p.Val272Ile)	AADACL2-AS1, SUCNR1 (V272I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3171942	NM_033050.6(SUCNR1):c.398T>C (p.Leu133Pro)	AADACL2-AS1, SUCNR1 (L133P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171941	NM_033050.6(SUCNR1):c.353T>C (p.Ile118Thr)	AADACL2-AS1, SUCNR1 (I118T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171940	NM_033050.6(SUCNR1):c.226C>T (p.Leu76Phe)	AADACL2-AS1, SUCNR1 (L76F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3171939	NM_033050.6(SUCNR1):c.224C>T (p.Thr75Ile)	AADACL2-AS1, SUCNR1 (T75I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600691	NM_033050.6(SUCNR1):c.87T>G (p.Phe29Leu)	AADACL2-AS1, SUCNR1 (F29L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530319	NM_033050.6(SUCNR1):c.650G>C (p.Arg217Thr)	AADACL2-AS1, SUCNR1 (R217T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520172	NM_033050.6(SUCNR1):c.245G>C (p.Ser82Thr)	AADACL2-AS1, SUCNR1 (S82T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515811	NM_033050.6(SUCNR1):c.67A>G (p.Lys23Glu)	AADACL2-AS1, SUCNR1 (K23E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496543	NM_033050.6(SUCNR1):c.682G>C (p.Glu228Gln)	AADACL2-AS1, SUCNR1 (E228Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408735	NM_033050.6(SUCNR1):c.95T>C (p.Ile32Thr)	AADACL2-AS1, SUCNR1 (I32T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385538	NM_033050.6(SUCNR1):c.817A>C (p.Ile273Leu)	AADACL2-AS1, SUCNR1 (I273L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378212	NM_033050.6(SUCNR1):c.502A>C (p.Asn168His)	AADACL2-AS1, SUCNR1 (N168H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335475	NM_033050.6(SUCNR1):c.747C>G (p.His249Gln)	AADACL2-AS1, SUCNR1 (H249Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318941	NM_033050.6(SUCNR1):c.168C>A (p.Asn56Lys)	AADACL2-AS1, SUCNR1 (N56K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292621	NM_033050.6(SUCNR1):c.367A>C (p.Ile123Leu)	AADACL2-AS1, SUCNR1 (I123L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2288935	NM_033050.6(SUCNR1):c.707T>A (p.Met236Lys)	AADACL2-AS1, SUCNR1 (M236K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235552	NM_033050.6(SUCNR1):c.531T>A (p.Ser177Arg)	AADACL2-AS1, SUCNR1 (S177R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232928	NM_033050.6(SUCNR1):c.346A>G (p.Ile116Val)	AADACL2-AS1, SUCNR1 (I116V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713065	NM_033050.6(SUCNR1):c.195C>T (p.Leu65=)	AADACL2-AS1, SUCNR1	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 21