rs767697161 Rat Genome Database

rs767697161 Rat Genome Database

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Variant: rs767697161 - Homo sapiens

RGD ID:

151745746

RS ID:

rs767697161

ClinVar ID:

CV1401753

Genic Status:

GENIC

Type:

SNV (SO:0001483)

Associated Genes:

Reference Nucleotide:

C

Variant Nucleotide:

A

Position

Assembly	Chr	Position
GRCh37	10	71,332,632
GRCh38	10	69,572,876

JBrowse:

View Region in Genome Browser (JBrowse)

Model

HGVS Name(s)	Last Evaluated	Molecular Consequence	Clinical Significance	Trait Synonyms
NM_020999.4:c.168G>T NC_000010.11:g.69572876C>A NC_000010.10:g.71332632C>A NP_066279.2:p.Gly56= NG_021321.1:g.5579G>T More...	07/12/2022	synonymous variant	likely benign\|uncertain significance	none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:	NEUROG3
Accession:	NM_020999
Location:	EXON
Amino Acid Prediction:	G to G (synonymous)
Amino Acid Position:	56

Amino Acid Sequence (Calculated using NCBI transcript definition)
MTPQPSGAPTVQVTRETERSFPRASEDEVTCPTSAPPSPTRTRGNCAEAEEGGCRGAPRKLRARRGGRSRPKSELALSKQ RRSRRKKANDRERNRMHNLNSALDALRGVLPTFPDDAKLTKIETLRFAHNYIWALTQTLRIADHSLYALEPPAPHCGELG SPGGSPGDWGSLYSPVSQAGSLSPAASLEERPGLLGATFSACLSPGSLAFSDFL*

Gene Symbol:	NEUROG3
Accession:	XM_017016280
Location:	EXON
Amino Acid Prediction:	G to G (synonymous)
Amino Acid Position:	56

Amino Acid Sequence (Calculated using NCBI transcript definition)
MTPQPSGAPTVQVTRETERSFPRASEDEVTCPTSAPPSPTRTRGNCAEAEEGGCRGAPRKLRARRGGRSRPKSELALSKQ RRSRRKKANDRERNRMHNLNSALDALRGVLPTFPDDAKLTKIETLRFAHNYIWALTQTLRIADHSLYALEPPAPHCGELG SPGGSPGDWGSLYSPVSQAGSLSPAASLEERPGLLGATFSACLSPGSLAFSDFL*

ClinVar GRCh37	ClinVar GRCh38

PMID:28492532

Database	Acc Id	Source(s)
ClinVar	RCV002042706	CLINVAR
dbSNP (RS)	rs767697161	CLINVAR
MedGen	C3661900	CLINVAR
NCBI Gene	NEUROG3	CLINVAR
OMIM	604882	CLINVAR