Variant #0000279577 (NC_000015.9:g.66777345G>A, NM_002755.3:c.711G>A (MAP2K1))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66777345G>A
DNA change (hg38) g.66485007G>A
Published as MAP2K1(NM_002755.3):c.711G>A (p.(Gly237=)), MAP2K1(NM_002755.4):c.711G>A (p.G237=)
ISCN -
DB-ID MAP2K1_000010 See all 2 reported entries
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) 0.01155 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 2018-01-15 20:58:59 +01:00 (CET)
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.711G>A r.(?) p.(Gly237=)
SNAPC5 NM_006049.2 -/. - c.*5732C>T r.(=) p.(=)


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