Variant #0000572105 (NC_000022.10:g.40814887C>T, NM_015705.4:c.*9124C>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.40814887C>T
DNA change (hg38) g.40418883C>T
Published as MRTFA(NM_001282662.2):c.1855G>A (p.E619K)
ISCN -
DB-ID MKL1_000011
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) 3.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGSM3 NM_015705.4 ?/. - c.*9124C>T r.(=) p.(=)
MKL1 NM_020831.3 ?/. - c.1555G>A r.(?) p.(Glu519Lys)


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