List of variants in gene TPM2 reported as likely pathogenic for arthrogryposis, distal, type 1A

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_003289.4(TPM2):c.142AAG[1] (p.Lys49del)	rs199476147
NM_003289.4(TPM2):c.180T>G (p.Tyr60Ter)	rs1281970248
NM_003289.4(TPM2):c.26A>C (p.Gln9Pro)	rs1554659746
NM_003289.4(TPM2):c.360TGA[1] (p.Asp121del)	rs1554658995
NM_003289.4(TPM2):c.364G>A (p.Glu122Lys)	rs2131853219
NM_003289.4(TPM2):c.382A>G (p.Lys128Glu)	rs1563929143
NM_003289.4(TPM2):c.41A>T (p.Asp14Val)	rs1825151618
NM_003289.4(TPM2):c.479G>T (p.Arg160Leu)
NM_003289.4(TPM2):c.493-2A>G	rs2131851980
NM_003289.4(TPM2):c.606C>A (p.Asn202Lys)	rs137853307

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