"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZMYM6"[ge - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3044803	NM_007167.4(ZMYM6):c.*3A>G	ZMYM6	Single nucleotide variant (3 prime UTR variant)	ZMYM6-related disorder	GBenign
Select item 3056816	NM_007167.4(ZMYM6):c.3697G>A (p.Glu1233Lys)	ZMYM6 (E1233K)	Single nucleotide variant (missense variant)	ZMYM6-related disorder	GBenign
Select item 3037478	NM_007167.4(ZMYM6):c.3318T>C (p.Asp1106=)	ZMYM6	Single nucleotide variant (synonymous variant)	ZMYM6-related disorder	GLikely benign
Select item 3052001	NM_007167.4(ZMYM6):c.3065T>C (p.Leu1022Ser)	ZMYM6 (L1022S)	Single nucleotide variant (missense variant)	ZMYM6-related disorder	GLikely benign
Select item 3035215	NM_007167.4(ZMYM6):c.3032T>G (p.Phe1011Cys)	ZMYM6 (F1011C)	Single nucleotide variant (missense variant)	ZMYM6-related disorder	GBenign
Select item 3044718	NM_007167.4(ZMYM6):c.3012A>G (p.Thr1004=)	ZMYM6	Single nucleotide variant (synonymous variant)	ZMYM6-related disorder	GLikely benign
Select item 3043412	NM_007167.4(ZMYM6):c.2912A>C (p.Asn971Thr)	ZMYM6 (N971T)	Single nucleotide variant (missense variant)	ZMYM6-related disorder	GLikely benign
Select item 3041852	NM_007167.4(ZMYM6):c.2806C>T (p.Arg936Cys)	ZMYM6 (R936C)	Single nucleotide variant (missense variant)	ZMYM6-related disorder	GBenign
Select item 713264	NM_007167.4(ZMYM6):c.2805T>C (p.Cys935=)	ZMYM6	Single nucleotide variant (synonymous variant)	ZMYM6-related disorder +1 more	GBenign
Select item 3037385	NM_007167.4(ZMYM6):c.2568T>C (p.Tyr856=)	ZMYM6	Single nucleotide variant (synonymous variant)	ZMYM6-related disorder	GBenign
Select item 3043128	NM_007167.4(ZMYM6):c.2210G>C (p.Arg737Thr)	ZMYM6 (R737T)	Single nucleotide variant (missense variant)	ZMYM6-related disorder	GBenign
Select item 3042312	NM_007167.4(ZMYM6):c.1979A>G (p.Lys660Arg)	ZMYM6 (K660R)	Single nucleotide variant (missense variant)	ZMYM6-related disorder	GLikely benign
Select item 3055336	NM_007167.4(ZMYM6):c.1878A>C (p.Pro626=)	ZMYM6	Single nucleotide variant (synonymous variant)	ZMYM6-related disorder	GLikely benign
Select item 3055374	NM_007167.4(ZMYM6):c.1814-4T>A	ZMYM6	Single nucleotide variant (intron variant)	ZMYM6-related disorder	GBenign
Select item 3041202	NM_007167.4(ZMYM6):c.1341+10G>A	ZMYM6	Single nucleotide variant (intron variant)	ZMYM6-related disorder	GBenign
Select item 3041172	NM_007167.4(ZMYM6):c.1091A>C (p.Asn364Thr)	ZMYM6 (N364T)	Single nucleotide variant (missense variant)	ZMYM6-related disorder	GBenign
Select item 3056208	NM_007167.4(ZMYM6):c.1002A>G (p.Leu334=)	ZMYM6	Single nucleotide variant (synonymous variant)	ZMYM6-related disorder	GBenign
Select item 712419	NM_007167.4(ZMYM6):c.179-5G>C	ZMYM6	Single nucleotide variant (intron variant)	ZMYM6-related disorder +1 more	GBenign
Select item 3033984	NM_007167.4(ZMYM6):c.94-4A>T	ZMYM6	Single nucleotide variant (intron variant)	ZMYM6-related disorder	GLikely benign
Select item 3057236	NM_007167.4(ZMYM6):c.94-5del	ZMYM6	Deletion (intron variant)	ZMYM6-related disorder	GBenign
Select item 3053011	NM_007167.4(ZMYM6):c.94-6_94-5del	ZMYM6	Deletion (intron variant)	ZMYM6-related disorder	GLikely benign
Select item 3041455	NM_007167.4(ZMYM6):c.82G>C (p.Asp28His)	ZMYM6 (D28H)	Single nucleotide variant (missense variant)	ZMYM6-related disorder	GLikely benign
Select item 3038869	NM_007167.4(ZMYM6):c.67A>G (p.Ile23Val)	ZMYM6 (I23V)	Single nucleotide variant (missense variant)	ZMYM6-related disorder	GBenign

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Items: 23