RGD:401891675 Rat Genome Database

RGD:401891675 Rat Genome Database

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Variant: RGD:401891675 - Homo sapiens

RGD ID:

401891675

ClinVar ID:

CV2780652

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

Reference Nucleotide:

G

Variant Nucleotide:

A

Position

Assembly	Chr	Position
GRCh37	16	14,766,603
GRCh38	16	14,672,746

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NM_001031688.1:c.359C>T NM_003561.3:c.359C>T NC_000016.10:g.14672746G>A NC_000016.9:g.14766603G>A More...	07/17/2023	missense variant	uncertain significance	AllHighlyPenetrant

Gene Symbol:	PLA2G10
Accession:	NM_003561
Location:	EXON
Amino Acid Prediction:	P to L (nonsynonymous)
Amino Acid Position:	120

Amino Acid Sequence (Calculated using NCBI transcript definition)
MGPLPVCLPIMLLLLLPSLLLLLLLPGPGSGEASRILRVHRRGILELAGTVGCVGPRTPIAYMKYGCFCGLGGHGQPRDA IDWCCHGHDCCYTRAEEAGCSPKTERYSWQCVNQSVLCGLAENKCQELLCKCDQEIANCLAQTEYNLKYLFYPQFLCEPD SPKCD*

Gene Symbol:	PLA2G10
Accession:	XM_047434757
Location:	EXON
Amino Acid Prediction:	P to L (nonsynonymous)
Amino Acid Position:	120

Amino Acid Sequence (Calculated using NCBI transcript definition)
MGPLPVCLPIMLLLLLPSLLLLLLLPGPGSGEASRILRVHRRGILELAGTVGCVGPRTPIAYMKYGCFCGLGGHGQPRDA IDWCCHGHDCCYTRAEEAGCSPKTERYSWQCVNQSVLCGLAENKCQELLCKCDQEIANCLAQTEYNLKYLFYPQFLCEPD SPKCD*

Gene Symbol:	PLA2G10
Accession:	NR_133651
Location:	EXON;NON-CODING

Gene Symbol:	PLA2G10
Accession:	XM_011522697
Location:	INTRON

Gene Symbol:	PLA2G10
Accession:	XM_011522695
Location:	INTRON

Gene Symbol:	PLA2G10
Accession:	XM_011522696
Location:	INTRON

Gene Symbol:	PLA2G10
Accession:	XM_011522698
Location:	INTRON

ClinVar GRCh37	ClinVar GRCh38

Database	Acc Id	Source(s)
ClinVar	RCV004352002	CLINVAR
MedGen	CN169374	CLINVAR
NCBI Gene	PLA2G10	CLINVAR
OMIM	603603	CLINVAR