Variant #0000527918 (NC_000006.11:g.161519378_161519383del, NM_005922.2:c.3593_3598del (MAP3K4))

Chromosome 6
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.161519378_161519383del
DNA change (hg38) g.161098346_161098351del
Published as MAP3K4(NM_005922.2):c.3566_3571del (p.(Ala1192_Ala1193del))
ISCN -
DB-ID MAP3K4_000006
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP3K4 NM_005922.2 -?/. - c.3593_3598del r.(?) p.(Ala1198_Ala1199del)


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