Variant #0000306736 (NC_000017.10:g.17696363G>A, NM_030665.3:c.101G>A (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.17696363G>A
DNA change (hg38) g.17793049G>A
Published as RAI1(NM_030665.3):c.101G>A (p.S34N), RAI1(NM_030665.4):c.101G>A (p.S34N)
ISCN -
DB-ID RAI1_000013 See all 2 reported entries
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) 7.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +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.*19573C>T r.(=) p.(=)
RAI1 NM_030665.3 -?/. - c.101G>A r.(?) p.(Ser34Asn)


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