Variant #0000331967 (NC_000007.13:g.150775948A>C, NM_003040.3:c.*2494A>C (SLC4A2))

Chromosome 7
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.150775948A>C
DNA change (hg38) g.151078861A>C
Published as FASTK(NM_006712.4):c.666T>G (p.(His222Gln))
ISCN -
DB-ID FASTK_000002
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) 0.00262 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A2 NM_003040.3 ?/. - c.*2494A>C r.(=) p.(=)
FASTK NM_006712.4 ?/. - c.666T>G r.(?) p.(His222Gln)
TMUB1 NM_031434.3 ?/. - c.*2688T>G r.(=) p.(=)


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