Variant #0000996067 (NC_000007.13:g.102108268A>C, NM_152892.1:c.676A>C (LRWD1))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.102108268A>C
DNA change (hg38) -
Published as LRWD1(NM_152892.1):c.676A>C (p.(Arg226Arg))
ISCN -
DB-ID ALKBH4_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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLR2J NM_006234.4 ?/. - c.*5828T>G r.(=) p.(=)
ALKBH4 NM_017621.3 ?/. - c.-2985T>G r.(?) p.(=)
LRWD1 NM_152892.1 ?/. - c.676A>C r.(?) p.(=)


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