Variant #0000964495 (NC_000007.13:g.150773255C>T, NM_003040.3:c.3627C>T (SLC4A2))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.150773255C>T
DNA change (hg38) -
Published as SLC4A2(NM_001199692.3):c.3627C>T (p.T1209=)
ISCN -
DB-ID FASTK_000005
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) 0.00927 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A2 NM_003040.3 -/. - c.3627C>T r.(?) p.(=)
FASTK NM_006712.4 -/. - c.*557G>A r.(=) p.(=)
TMUB1 NM_031434.3 -/. - c.*5381G>A r.(=) p.(=)


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