Variant #0000278479 (NC_000007.13:g.138603302G>T, NM_001164665.1:c.1070C>A (KIAA1549))

Chromosome 7
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.138603302G>T
DNA change (hg38) g.138918556G>T
Published as KIAA1549(NM_001164665.1):c.1070C>A (p.T357K), KIAA1549(NM_001164665.2):c.1070C>A (p.T357K)
ISCN -
DB-ID KIAA1549_000043 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) 0.00019 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA1549 NM_001164665.1 -?/. - c.1070C>A r.(?) p.(Thr357Lys)


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