Variant #0000616636 (NC_000017.10:g.43345027C>G, NM_003954.3:c.2072G>C (MAP3K14))

Chromosome 17
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.43345027C>G
DNA change (hg38) g.45267660C>G
Published as MAP3K14(NM_003954.5):c.2072G>C (p.R691T)
ISCN -
DB-ID MAP3K14_000014
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP3K14 NM_003954.3 -?/. - c.2072G>C r.(?) p.(Arg691Thr)
SPATA32 NM_152343.2 -?/. - c.-5644G>C r.(?) p.(=)
MAP3K14-AS1 NR_024434.1 -?/. - n.284+332C>G r.(?) -


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