Variant #0000657636 (NC_000015.9:g.66782113_66782116del, NC_000015.9(NM_002755.3):c.1068+12_1068+15del (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.66782113_66782116del
DNA change (hg38) g.66489775_66489778del
Published as MAP2K1(NM_002755.3):c.1068+12_1068+15delTATT, MAP2K1(NM_002755.4):c.1068+12_1068+15delTATT
ISCN -
DB-ID MAP2K1_000021 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +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.1068+12_1068+15del r.(=) p.(=)
SNAPC5 NM_006049.2 -/. - c.*965_*968del r.(=) p.(=)


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