rs141595181 Rat Genome Database

rs141595181 Rat Genome Database

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Variant: rs141595181 - Homo sapiens

RGD ID:

14711372

RS ID:

rs141595181

ClinVar ID:

CV632477

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

HNRNPDL LOC127401069

Reference Nucleotide:

G

Variant Nucleotide:

A

Position

Assembly	Chr	Position
GRCh37	4	83,350,507
GRCh38	4	82,429,354

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NP_112740.1:p.Pro113Ser NM_031372.3:c.337C>T NM_031372.4:c.337C>T NC_000004.11:g.83350507G>A More...	08/10/2023	missense variant	uncertain significance	AllHighlyPenetrant; Limb-girdle muscular dystrophy, type 1G; MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 3

Object Symbol	Species	Term	Qualifier	Evidence	With	Reference	Notes	Source	Original Reference(s)
CV632477	Human	autosomal dominant limb-girdle muscular dystrophy type 3		IAGP		8554872	ClinVar Annotator: match by term: Limb-girdle muscular dystrophy, type 1G	ClinVar	PMID:28492532

Gene Symbol:	HNRNPDL
Accession:	NM_001207000
Location:	EXON
Amino Acid Prediction:	P to S (nonsynonymous)
Amino Acid Position:	113

Amino Acid Sequence (Calculated using NCBI transcript definition)
MEVPPRLSHVPPPLFPSAPATLASRSLSHWRPRPPRQLAPLLPSLAPSSARQGARRAQRHVTAQQPSRLAGGAAIKGGRR RRPDLFRRHFKSSSIQRSAAAAAATRTARQHPSADSSVTMEDMNEYSNIEEFAEGSKINASKNQQDDGKMFIGGLSWDTS KKDLTEYLSRFGEVVDCTIKTDPVTGRSRGFGFVLFKDAASVDKVLELKEHKLDGKLIDPKRAKALKGKEPPKKVFVGGL SPDTSEEQIKEYFGAFGEIENIELPMDTKTNERRGFCFITYTDEEPVKKLLESRYHQIGSGKCEIKVAQPKEVYRQQQQQ QKGGRGAAAGGRGGTRGRGRGQQSTYGKASRGGGNHQNNYQPY*

Gene Symbol:	HNRNPDL
Accession:	NM_031372
Location:	EXON
Amino Acid Prediction:	P to S (nonsynonymous)
Amino Acid Position:	113

Amino Acid Sequence (Calculated using NCBI transcript definition)
MEVPPRLSHVPPPLFPSAPATLASRSLSHWRPRPPRQLAPLLPSLAPSSARQGARRAQRHVTAQQPSRLAGGAAIKGGRR RRPDLFRRHFKSSSIQRSAAAAAATRTARQHPSADSSVTMEDMNEYSNIEEFAEGSKINASKNQQDDGKMFIGGLSWDTS KKDLTEYLSRFGEVVDCTIKTDPVTGRSRGFGFVLFKDAASVDKVLELKEHKLDGKLIDPKRAKALKGKEPPKKVFVGGL SPDTSEEQIKEYFGAFGEIENIELPMDTKTNERRGFCFITYTDEEPVKKLLESRYHQIGSGKCEIKVAQPKEVYRQQQQQ QKGGRGAAAGGRGGTRGRGRGQGQNWNQGFNNYYDQGYGNYNSAYGGDQNYSGYGGYDYTGYNYGNYGYGQGYADYSGQQ STYGKASRGGGNHQNNYQPY*

Gene Symbol:	HNRNPDL
Accession:	NR_003249
Location:	EXON;NON-CODING

ClinVar GRCh37	ClinVar GRCh38

PMID:28492532

Database	Acc Id	Source(s)
ClinVar	RCV000817568	CLINVAR
	RCV004028918	CLINVAR
dbSNP (RS)	rs141595181	CLINVAR
MedGen	C1836765	CLINVAR
	CN169374	CLINVAR
NCBI Gene	HNRNPDL	CLINVAR
OMIM	607137	CLINVAR
	609115	CLINVAR