Variant #0000681900 (NC_000022.10:g.40815138G>A, NM_015705.4:c.*9375G>A (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.40815138G>A
DNA change (hg38) -
Published as MRTFA(NM_001282662.2):c.1604C>T (p.T535M)
ISCN -
DB-ID MKL1_000027
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) 1.0E-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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGSM3 NM_015705.4 ?/. - c.*9375G>A r.(=) p.(=)
MKL1 NM_020831.3 ?/. - c.1304C>T r.(?) p.(Thr435Met)


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