Variant #0000288887 (NC_000006.11:g.42147102C>T, NM_000409.3:c.567C>T (GUCA1A))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.42147102C>T
DNA change (hg38) g.42179364C>T
Published as GUCA1A(NM_000409.4):c.567C>T (p.D189=)
ISCN -
DB-ID GUCA1A_000008
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) 0.0033 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-19 11:57:21 +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.567C>T r.(?) p.(Asp189=)
GUCA1B NM_002098.5 -?/. - c.*5451G>A r.(=) p.(=)


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