Variant #0000866423 (NC_000020.10:g.3219781C>G, NM_032034.3:c.-1456G>C (SLC4A11))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3219781C>G
DNA change (hg38) -
Published as SLC4A11(NM_001174089.1):c.3G>C (p.M1?)
ISCN -
DB-ID SLC4A11_000101
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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A11 NM_001174089.1 +?/. - c.3G>C r.(?) p.(Met1?)
SLC4A11 NM_032034.3 +?/. - c.-1456G>C r.(?) p.(=)


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