Variant #0000806874 (NC_000015.9:g.66782110A>G, NC_000015.9(NM_002755.3):c.1068+9A>G (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.66782110A>G
DNA change (hg38) -
Published as MAP2K1(NM_002755.3):c.1068+9A>G, MAP2K1(NM_002755.4):c.1068+9A>G
ISCN -
DB-ID MAP2K1_000033 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) 0.00029 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP2K1 NM_002755.3 -?/. - c.1068+9A>G r.(=) p.(=)
SNAPC5 NM_006049.2 -?/. - c.*967T>C r.(=) p.(=)


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