Variant #0000308668 (NC_000007.13:g.127341296T>G, NM_022143.4:c.*327436A>C (LRRC4))

Chromosome 7
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.127341296T>G
DNA change (hg38) g.127701242T>G
Published as SND1(NM_014390.3):c.508T>G (p.S170A), SND1(NM_014390.4):c.508T>G (p.(Ser170Ala))
ISCN -
DB-ID SND1_000001 See all 2 reported entries
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) 0.00017 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 2026-01-20 18:57:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SND1 NM_014390.2 -?/. - c.508T>G r.(?) p.(Ser170Ala)
LRRC4 NM_022143.4 -?/. - c.*327436A>C r.(=) p.(=)


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