Variant #0000514569 (NC_000002.11:g.219130676T>C, NM_001077399.2:c.-4583T>C (PNKD))

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.219130676T>C
DNA change (hg38) g.218265953T>C
Published as AAMP(NM_001087.3):c.764-7A>G (p.(=))
ISCN -
DB-ID AAMP_000002
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) 0.00091 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 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     
GPBAR1 NM_001077191.1 -?/. - c.*2236T>C r.(=) p.(=)
PNKD NM_001077399.2 -?/. - c.-4583T>C r.(?) p.(=)
AAMP NM_001087.3 -?/. - c.764-7A>G r.(=) p.(=)
TMBIM1 NM_022152.4 -?/. - c.*9522A>G r.(=) p.(=)


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