"GeneDx"[submitter] AND "LOC130057222"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 668731	NM_001018005.2(TPM1):c.240+4065A>G	LOC130057222, TPM1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1205060	NM_001018005.2(TPM1):c.240+4092C>G	LOC130057222, TPM1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 669005	NM_001018005.2(TPM1):c.240+4118C>G	LOC130057222, TPM1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1263877	NM_001018005.2(TPM1):c.240+4144T>C	LOC130057222, TPM1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 671947	NM_001018005.2(TPM1):c.240+4218C>T	LOC130057222, TPM1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1259669	NM_001018005.2(TPM1):c.240+4256T>C	LOC130057222, TPM1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 672965	NM_001018005.2(TPM1):c.240+4268A>C	LOC130057222, TPM1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1232571	NM_001018005.2(TPM1):c.240+4296A>G	LOC130057222, TPM1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 675680	NM_001018005.2(TPM1):c.240+4332del	LOC130057222, TPM1 +1 more	Deletion (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1290393	NM_001018005.2(TPM1):c.240+4354C>T	LOC130057222, TPM1 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GBenign
Select item 382288	NM_001018005.2(TPM1):c.240+4389A>C	LOC130057222, TPM1 +1 more	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign
Select item 379186	NM_001018005.2(TPM1):c.240+4447G>C	LOC130057222, TPM1 +1 more (E8D)	Single nucleotide variant (intron variant +2 more)	not specified	GLikely benign
Select item 181655	NM_001018005.2(TPM1):c.240+4465C>G	LOC130057222, TPM1 +1 more (I14M)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 1256862	NM_001018005.2(TPM1):c.240+4638_240+4639insG	LOC130057222, TPM1 +1 more	Insertion (intron variant)	not provided	GBenign
Select item 1208957	NM_001018005.2(TPM1):c.240+4638C>T	LOC130057222, TPM1 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1290394	NM_001018005.2(TPM1):c.240+4640dup	LOC130057222, TPM1 +1 more	Duplication (intron variant)	not provided	GBenign
Select item 1231120	NM_001018005.2(TPM1):c.240+4639C>T	LOC130057222, TPM1 +1 more	Single nucleotide variant (intron variant)	not provided	GBenign