Variant #0000983772 (NC_000020.10:g.3209500C>T, NM_032034.3:c.2224G>A (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.3209500C>T
DNA change (hg38) -
Published as SLC4A11(NM_001174089.2):c.2176G>A (p.(Gly726Arg))
ISCN -
DB-ID SLC4A11_000025 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) 0.00032 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.2176G>A r.(?) p.(Gly726Arg)
SLC4A11 NM_032034.3 ?/. - c.2224G>A r.(?) p.(Gly742Arg)
ITPA NM_033453.3 ?/. - c.*5392C>T r.(=) p.(=)


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