Variant #0000692372 (NC_000017.10:g.42337247C>T, NM_000342.3:c.539G>A (SLC4A1))

Chromosome 17
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.42337247C>T
DNA change (hg38) -
Published as SLC4A1(NM_000342.3):c.539G>A (p.R180H, p.(Arg180His)), SLC4A1(NM_000342.4):c.539G>A (p.R180H)
ISCN -
DB-ID SLC4A1_000024 See all 4 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) 0.00344 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A1 NM_000342.3 -?/. - c.539G>A r.(?) p.(Arg180His)


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