Variant #0000249102 (NC_000007.13:g.103053435A>G, NC_000007.13(NM_198999.2):c.403+14T>C (SLC26A5))

Chromosome 7
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.103053435A>G
DNA change (hg38) g.103412988A>G
Published as SLC26A5(NM_198999.3):c.403+14T>C
ISCN -
DB-ID SLC26A5_000009 See all 2 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) 0.30448 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.*44934A>G r.(=) p.(=)
SLC26A5 NM_198999.2 -/. - c.403+14T>C r.(=) p.(=)


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