Variant #0000560546 (NC_000017.10:g.17719179T>C, NM_030665.3:c.*5884T>C (RAI1))

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.17719179T>C
DNA change (hg38) g.17815865T>C
Published as SREBF1(NM_001005291.2):c.2468A>G (p.(Asn823Ser))
ISCN -
DB-ID RAI1_000138
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) 0.00011 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 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     
SREBF1 NM_004176.4 -?/. - c.2378A>G r.(?) p.(Asn793Ser)
RAI1 NM_030665.3 -?/. - c.*5884T>C r.(=) p.(=)


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