Variant #0000617556 (NC_000019.9:g.3637485C>T, NC_000019.9(NM_012398.2):c.1920+1397G>A (PIP5K1C))

Chromosome 19
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.3637485C>T
DNA change (hg38) g.3637487C>T
Published as PIP5K1C(NM_001300849.1):c.2047G>A (p.G683R)
ISCN -
DB-ID PIP5K1C_000014
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIP5K1C NM_012398.2 -?/. - c.1920+1397G>A r.(=) p.(=)


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