Variant #0000621487 (NC_000005.9:g.139892433A>G, NM_017747.2:c.4125A>G (ANKHD1))

Chromosome 5
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.139892433A>G
DNA change (hg38) g.140512848A>G
Published as ANKHD1(NM_017747.3):c.4125A>G (p.Q1375=), ANKHD1-EIF4EBP3(NM_020690.5):c.4125A>G (p.Q1375=)
ISCN -
DB-ID ANKHD1_000005
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) 0.00032 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF4EBP3 NM_003732.2 -?/. - c.-34890A>G r.(?) p.(=)
ANKHD1 NM_017747.2 -?/. - c.4125A>G r.(?) p.(Gln1375=)
ANKHD1-EIF4EBP3 NM_020690.5 -?/. - c.4125A>G r.(?) p.(Gln1375=)


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