Variant #0000516078 (NC_000002.11:g.46839434T>C, NM_014171.4:c.-4988T>C (CRIPT))

Chromosome 2
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.46839434T>C
DNA change (hg38) g.46612295T>C
Published as PIGF(NM_002643.3):c.370A>G (p.(Thr124Ala))
ISCN -
DB-ID CRIPT_000003
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) 0.00204 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIGF NM_002643.3 -?/. - c.370A>G r.(?) p.(Thr124Ala)
RHOQ NM_012249.3 -?/. - c.*31212T>C r.(=) p.(=)
CRIPT NM_014171.4 -?/. - c.-4988T>C r.(?) p.(=)


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