Variant #0001057171 (NC_000022.10:g.40805731C>T, NM_015705.4:c.2218C>T (SGSM3))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.40805731C>T
DNA change (hg38) -
Published as SGSM3(NM_015705.6):c.2218C>T (p.(His740Tyr))
ISCN -
DB-ID MKL1_000049
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 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 2025-11-01 13:22:20 +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.2218C>T r.(?) p.(His740Tyr)
MKL1 NM_020831.3 ?/. - c.*1663G>A r.(=) p.(=)


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