Variant #0000291112 (NC_000004.11:g.110769387C>A, NM_198506.4:c.30C>A (LRIT3))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.110769387C>A
DNA change (hg38) g.109848231C>A
Published as LRIT3(NM_198506.4):c.30C>A (p.V10=)
ISCN -
DB-ID LRIT3_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00016 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-16 14:26:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RRH NM_006583.2 -?/. - c.*4034C>A r.(=) p.(=)
LRIT3 NM_198506.4 -?/. - c.30C>A r.(?) p.(Val10=)


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