Related gene-specific medical variations for Gene (Select 100128264) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3107588	NM_024012.4(HTR5A):c.68G>C (p.Ser23Thr)	HTR5A, HTR5A-AS1 (S23T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107586	NM_024012.4(HTR5A):c.190A>G (p.Thr64Ala)	HTR5A, HTR5A-AS1 (T64A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2594695	NM_024012.4(HTR5A):c.110C>T (p.Ser37Leu)	HTR5A, HTR5A-AS1 (S37L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554608	NM_024012.4(HTR5A):c.398C>T (p.Thr133Met)	HTR5A, HTR5A-AS1 (T133M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2457920	NM_024012.4(HTR5A):c.181G>T (p.Val61Leu)	HTR5A, HTR5A-AS1 (V61L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2348348	NM_024012.4(HTR5A):c.121G>A (p.Val41Met)	HTR5A-AS1, HTR5A (V41M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307953	NM_024012.4(HTR5A):c.205C>G (p.Arg69Gly)	HTR5A, HTR5A-AS1 (R69G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2238001	NM_024012.4(HTR5A):c.484A>G (p.Ile162Val)	HTR5A, HTR5A-AS1 (I162V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 787326	NM_024012.4(HTR5A):c.621C>T (p.Gly207=)	HTR5A, HTR5A-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 783512	NM_024012.4(HTR5A):c.300C>T (p.His100=)	HTR5A, HTR5A-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 708987	NM_024012.4(HTR5A):c.567C>T (p.Ser189=)	HTR5A, HTR5A-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 161768	NM_024012.4(HTR5A):c.79G>C (p.Asp27His)	HTR5A, HTR5A-AS1 (D27H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance