List of variants in gene DYNLT2 studied for not specified

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_174910.3(DYNLT2):c.559G>A (p.Val187Met)	rs144598809	0.00098
NM_174910.3(DYNLT2):c.491C>T (p.Ala164Val)	rs375109366	0.00029
NM_174910.3(DYNLT2):c.250G>T (p.Ala84Ser)	rs147456843	0.00019
NM_174910.3(DYNLT2):c.148A>G (p.Arg50Gly)	rs148750299	0.00018
NM_174910.3(DYNLT2):c.202G>A (p.Ala68Thr)	rs550264282	0.00007
NM_174910.3(DYNLT2):c.589T>C (p.Tyr197His)	rs201340121	0.00004
NM_174910.3(DYNLT2):c.310G>A (p.Val104Ile)	rs750779623	0.00003
NM_174910.3(DYNLT2):c.137G>C (p.Arg46Thr)	rs747605467	0.00002
NM_174910.3(DYNLT2):c.164A>G (p.Asn55Ser)	rs750219247	0.00002
NM_174910.3(DYNLT2):c.347A>G (p.Lys116Arg)	rs954938215	0.00001
NM_174910.3(DYNLT2):c.206A>G (p.Asp69Gly)
NM_174910.3(DYNLT2):c.214A>G (p.Lys72Glu)
NM_174910.3(DYNLT2):c.341A>G (p.Asp114Gly)	rs762166347
NM_174910.3(DYNLT2):c.394C>T (p.Arg132Cys)
NM_174910.3(DYNLT2):c.431G>A (p.Arg144His)
NM_174910.3(DYNLT2):c.557A>G (p.Tyr186Cys)

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