Variant #0000308356 (NC_000007.13:g.107302088T>C, NM_000441.1:c.2T>C (SLC26A4))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.107302088T>C
DNA change (hg38) g.107661643T>C
Published as SLC26A4(NM_000441.1):c.2T>C (p.M1?)
ISCN -
DB-ID SLC26A4_000202 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) 7.0E-5 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 13:20:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC26A4 NM_000441.1 +/. - c.2T>C r.(?) p.(Met1?)
SLC26A4-AS1 NR_028137.1 +/. - n.156A>G r.(?) -


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