Variant #0000887693 (NC_000007.13:g.138602716G>A, NM_001164665.1:c.1656C>T (KIAA1549))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.138602716G>A
DNA change (hg38) -
Published as KIAA1549(NM_001164665.1):c.1656C>T (p.S552=), KIAA1549(NM_020910.3):c.1656C>T (p.S552=)
ISCN -
DB-ID KIAA1549_000036 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) 0.00184 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA1549 NM_001164665.1 -/. - c.1656C>T r.(?) p.(Ser552=)


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