Variant #0000322307 (NC_000011.9:g.64898466T>G, NM_004927.3:c.*5122T>G (MRPL49))

Chromosome 11
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.64898466T>G
DNA change (hg38) g.65130995T>G
Published as SYVN1(NM_032431.2):c.866A>C (p.(Asn289Thr))
ISCN -
DB-ID SYVN1_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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +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     
FAU NM_001997.4 -?/. - c.-8913A>C r.(?) p.(=)
MRPL49 NM_004927.3 -?/. - c.*5122T>G r.(=) p.(=)
SYVN1 NM_032431.2 -?/. - c.866A>C r.(?) p.(Asn289Thr)


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