Variant #0000308359 (NC_000007.13:g.103018075C>T, NM_198999.2:c.1957G>A (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.103018075C>T
DNA change (hg38) g.103377628C>T
Published as SLC26A5(NM_198999.2):c.1957G>A (p.D653N)
ISCN -
DB-ID SLC26A5_000005
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) Retrieve
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMC2 NM_002803.3 ?/. - c.*9574C>T r.(=) p.(=)
SLC26A5 NM_198999.2 ?/. - c.1957G>A r.(?) p.(Asp653Asn)


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