Variant #0000254550 (NC_000007.13:g.103029848A>G, NM_198999.2:c.1335T>C (SLC26A5))

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.103029848A>G
DNA change (hg38) g.103389401A>G
Published as SLC26A5(NM_198999.2):c.1335T>C (p.I445=)
ISCN -
DB-ID SLC26A5_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) 0.00354 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-23 13:02:59 +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.*21347A>G r.(=) p.(=)
SLC26A5 NM_198999.2 -?/. - c.1335T>C r.(?) p.(Ile445=)


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