Variant #0000324159 (NC_000015.9:g.66787688C>A, NM_002755.3:c.*4735C>A (MAP2K1))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.66787688C>A
DNA change (hg38) g.66495350C>A
Published as SNAPC5(NM_006049.2):c.160G>T (p.(Val54Leu))
ISCN -
DB-ID SNAPC5_000001
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 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 2018-01-15 20:58:59 +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     
RPL4 NM_000968.3 ?/. - c.*4057G>T r.(=) p.(=)
MAP2K1 NM_002755.3 ?/. - c.*4735C>A r.(=) p.(=)
SNAPC5 NM_006049.2 ?/. - c.160G>T r.(?) p.(Val54Leu)
ZWILCH NM_017975.3 ?/. - c.-9989C>A r.(?) p.(=)


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