Variant #0000951614 (NC_000022.10:g.40814749C>T, NM_015705.4:c.*8986C>T (SGSM3))

Chromosome 22
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.40814749C>T
DNA change (hg38) -
Published as MRTFA(NM_001282662.2):c.1993G>A (p.A665T), MRTFA(NM_020831.6):c.1993G>A (p.A665T)
ISCN -
DB-ID MKL1_000004 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +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     
SGSM3 NM_015705.4 -/. - c.*8986C>T r.(=) p.(=)
MKL1 NM_020831.3 -/. - c.1693G>A r.(?) p.(Ala565Thr)


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