List of variants in gene LOC132089829, MYPN studied for Dilated cardiomyopathy 1KK

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_032578.4(MYPN):c.3075+21G>A	rs7081213	0.41962
NM_032578.4(MYPN):c.3075+10C>G	rs1230004902	0.00008
NM_032578.4(MYPN):c.3065C>G (p.Ala1022Gly)	rs773991025	0.00007
NM_032578.4(MYPN):c.3039C>T (p.Asp1013=)	rs748080770	0.00002
NM_032578.4(MYPN):c.3040G>A (p.Asp1014Asn)	rs769591145	0.00001
NM_032578.4(MYPN):c.3060G>A (p.Met1020Ile)	rs762642659	0.00001
NM_032578.4(MYPN):c.3074A>G (p.Gln1025Arg)	rs759171149	0.00001
NM_032578.4(MYPN):c.3075+20C>T	rs377273417	0.00001
NM_032578.4(MYPN):c.3075+8C>T	rs767145495	0.00001
NM_032578.4(MYPN):c.3075+9G>A	rs370764417	0.00001
NM_032578.4(MYPN):c.3032G>A (p.Ser1011Asn)
NM_032578.4(MYPN):c.3048C>T (p.Asn1016=)
NM_032578.4(MYPN):c.3054C>T (p.Thr1018=)
NM_032578.4(MYPN):c.3057del (p.Met1020fs)	rs2134278222
NM_032578.4(MYPN):c.3063A>G (p.Ala1021=)
NM_032578.4(MYPN):c.3068A>G (p.Asn1023Ser)	rs905631355
NM_032578.4(MYPN):c.3075+13G>C	rs1271146904
NM_032578.4(MYPN):c.3075+15T>C
NM_032578.4(MYPN):c.3075+5_3075+13del	rs864622652

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