Variant #0000977440 (NC_000007.13:g.103053497G>A, NM_198999.2:c.355C>T (SLC26A5))

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.103053497G>A
DNA change (hg38) -
Published as SLC26A5(NM_198999.3):c.355C>T (p.(Pro119Ser))
ISCN -
DB-ID SLC26A5_000002 See all 3 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 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMC2 NM_002803.3 ?/. - c.*44996G>A r.(=) p.(=)
SLC26A5 NM_198999.2 ?/. - c.355C>T r.(?) p.(Pro119Ser)


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