Variant #0000887249 (NC_000006.11:g.42146619A>C, NM_000409.3:c.431A>C (GUCA1A))

Chromosome 6
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.42146619A>C
DNA change (hg38) -
Published as LOC118142757(NM_001319061.2):c.431A>C (p.D144A)
ISCN -
DB-ID GUCA1A_000059
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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GUCA1A NM_000409.3 ?/. - c.431A>C r.(?) p.(Asp144Ala)
GUCA1B NM_002098.5 ?/. - c.*5934T>G r.(=) p.(=)


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