Variant #0000530026 (NC_000007.13:g.100175361C>G, NM_002319.3:c.1042G>C (LRCH4))

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.100175361C>G
DNA change (hg38) g.100577738C>G
Published as LRCH4(NM_002319.3):c.1042G>C (p.(Asp348His))
ISCN -
DB-ID SAP25_000002
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SAP25 NM_001168682.1 -?/. - c.-4269G>C r.(?) p.(=)
LRCH4 NM_002319.3 -?/. - c.1042G>C r.(?) p.(Asp348His)


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