Variant #0000528846 (NC_000006.11:g.42146147G>A, NM_000409.3:c.331G>A (GUCA1A))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.42146147G>A
DNA change (hg38) g.42178409G>A
Published as LOC118142757(NM_000409.5):c.331G>A (p.E111K)
ISCN -
DB-ID GUCA1A_000017
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GUCA1A NM_000409.3 +/. - c.331G>A r.(?) p.(Glu111Lys)
GUCA1B NM_002098.5 +/. - c.*6406C>T r.(=) p.(=)


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