Variant #0000691834 (NC_000015.9:g.66679691C>T, NM_002755.3:c.6C>T (MAP2K1))

Chromosome 15
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.66679691C>T
DNA change (hg38) -
Published as MAP2K1(NM_002755.4):c.6C>T (p.P2=)
ISCN -
DB-ID MAP2K1_000028
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) 0.0001 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP2K1 NM_002755.3 -?/. - c.6C>T r.(?) p.(Pro2=)
SNAPC5 NM_006049.2 -?/. - c.*103386G>A r.(=) p.(=)
TIPIN NM_017858.2 -?/. - c.-30723G>A r.(?) p.(=)


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