Variant #0000866421 (NC_000020.10:g.3212175A>G, NM_032034.3:c.797T>C (SLC4A11))

Chromosome 20
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.3212175A>G
DNA change (hg38) -
Published as SLC4A11(NM_001174090.1):c.878T>C (p.M293T)
ISCN -
DB-ID SLC4A11_000098
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 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A11 NM_001174089.1 ?/. - c.749T>C r.(?) p.(Met250Thr)
SLC4A11 NM_032034.3 ?/. - c.797T>C r.(?) p.(Met266Thr)
ITPA NM_033453.3 ?/. - c.*8067A>G r.(=) p.(=)


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