Variant #0000566325 (NC_000019.9:g.14516668A>T, NM_078481.3:c.1738A>T (CD97))

Chromosome 19
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.14516668A>T
DNA change (hg38) g.14405856A>T
Published as CD97(NM_001025160.2):c.1591A>T (p.(Thr531Ser))
ISCN -
DB-ID CD97_000003
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDX39A NM_005804.3 -?/. - c.*3080T>A r.(=) p.(=)
CD97 NM_078481.3 -?/. - c.1738A>T r.(?) p.(Thr580Ser)


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