Variant #0000277521 (NC_000006.11:g.42146963C>A, NC_000006.11(NM_000409.3):c.446-18C>A (GUCA1A))

Chromosome 6
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.42146963C>A
DNA change (hg38) g.42179225C>A
Published as LOC118142757(NM_001319061.2):c.446-18C>A
ISCN -
DB-ID GUCA1A_000006
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) 0.00221 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.446-18C>A r.(=) p.(=)
GUCA1B NM_002098.5 -/. - c.*5590G>T r.(=) p.(=)


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