Variant #0000609188 (NC_000004.11:g.25664244G>A, SLC34A2(NM_006424.2):c.112+10G>A)

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.25664244G>A
DNA change (hg38) g.25662622G>A
Published as SLC34A2(NM_001177999.1):c.112+10G>A
ISCN -
DB-ID SLC34A2_000007
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) 0.0739 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC34A2 NM_006424.2 -/. - c.112+10G>A r.(=) p.(=)