Variant #0000569431 (NC_000020.10:g.3214276T>C, NM_032034.3:c.661A>G (SLC4A11))

Chromosome 20
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.3214276T>C
DNA change (hg38) g.3233630T>C
Published as SLC4A11(NM_001174090.1):c.742A>G (p.M248V)
ISCN -
DB-ID SLC4A11_000084
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) 2.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
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     
SLC4A11 NM_001174089.1 -?/. - c.613A>G r.(?) p.(Met205Val)
SLC4A11 NM_032034.3 -?/. - c.661A>G r.(?) p.(Met221Val)


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