Variant #0000689855 (NC_000007.13:g.107302114C>A, NM_000441.1:c.28C>A (SLC26A4))

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.107302114C>A
DNA change (hg38) -
Published as SLC26A4(NM_000441.1):c.28C>A (p.P10T)
ISCN -
DB-ID SLC26A4_000239
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) 0.00015 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 2020-09-15 15:50:26 +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     
SLC26A4 NM_000441.1 -?/. - c.28C>A r.(?) p.(Pro10Thr)
SLC26A4-AS1 NR_028137.1 -?/. - n.130G>T r.(?) -


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