"Ambry Genetics"[submitter] AND "HYCC2"[gene] - ClinVar

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

Search results

Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3107707	NM_001321623.1(HYCC2):c.1672G>A (p.Glu558Lys)	HYCC2, LOC105373835 (E502K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107706	NM_001321623.1(HYCC2):c.1625G>A (p.Arg542Gln)	HYCC2, LOC105373835 (R460Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107705	NM_001321623.1(HYCC2):c.1535C>T (p.Ser512Leu)	HYCC2, LOC105373835 (S512L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107704	NM_001321623.1(HYCC2):c.1471C>G (p.Gln491Glu)	HYCC2, LOC105373835 (Q353E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107703	NM_001321623.1(HYCC2):c.1441A>G (p.Met481Val)	HYCC2, LOC105373835 (M425V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493082	NM_001321623.1(HYCC2):c.1385A>G (p.Lys462Arg)	HYCC2, LOC105373835 (K406R +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3107702	NM_001321623.1(HYCC2):c.1381C>T (p.Arg461Cys)	HYCC2, LOC105373835 (R379C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107701	NM_001321623.1(HYCC2):c.1372T>G (p.Ser458Ala)	HYCC2, LOC105373835 (S320A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621570	NM_001321623.1(HYCC2):c.1361G>C (p.Ser454Thr)	HYCC2, LOC105373835 (S316T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285122	NM_001321623.1(HYCC2):c.1319C>T (p.Ala440Val)	HYCC2, LOC105373835 (A440V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285121	NM_001321623.1(HYCC2):c.1238T>C (p.Leu413Pro)	HYCC2, LOC105373835 (L413P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107719	NM_001321623.1(HYCC2):c.971G>A (p.Arg324His)	HYCC2, LOC105373835 (R242H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483028	NM_001321623.1(HYCC2):c.871C>G (p.Pro291Ala)	HYCC2, LOC105373835 (P209A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486399	NM_001321623.1(HYCC2):c.713T>C (p.Val238Ala)	HYCC2, LOC105373835 (V156A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488093	NM_001321623.1(HYCC2):c.650G>A (p.Arg217Gln)	HYCC2, LOC105373835 (R217Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107718	NM_001321623.1(HYCC2):c.560G>A (p.Cys187Tyr)	HYCC2, LOC105373835 (C105Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107717	NM_001321623.1(HYCC2):c.557T>A (p.Leu186Gln)	HYCC2, LOC105373835 (L104Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107716	NM_001321623.1(HYCC2):c.437C>T (p.Ala146Val)	HYCC2, LOC105373835 (A64V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3107714	NM_001321623.1(HYCC2):c.383C>T (p.Pro128Leu)	HYCC2, LOC105373835 (P46L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107713	NM_001321623.1(HYCC2):c.340G>T (p.Ala114Ser)	HYCC2, LOC105373835 (A114S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107712	NM_001321623.1(HYCC2):c.302T>C (p.Ile101Thr)	HYCC2, LOC105373835 (I19T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3107711	NM_001321623.1(HYCC2):c.209G>A (p.Arg70Gln)	HYCC2, LOC105373835 (R70Q)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3107710	NM_001321623.1(HYCC2):c.191A>G (p.Tyr64Cys)	HYCC2, LOC105373835 (Y64C)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2490063	NM_001321623.1(HYCC2):c.166G>C (p.Val56Leu)	HYCC2, LOC105373835 (V56L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3107709	NM_001321623.1(HYCC2):c.151G>A (p.Glu51Lys)	HYCC2 (E51K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3107720	NM_001321623.1(HYCC2):c.98G>A (p.Arg33Gln)	HYCC2 (R33Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3107715	NM_001321623.1(HYCC2):c.39A>T (p.Leu13Phe)	HYCC2 (L13F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 27