Variant #0000572108 (NC_000022.10:g.40815120A>C, NM_015705.4:c.*9357A>C (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.40815120A>C
DNA change (hg38) g.40419116A>C
Published as MKL1(NM_020831.3):c.1322T>G (p.(Val441Gly)), MRTFA(NM_001282662.2):c.1622T>G (p.V541G)
ISCN -
DB-ID MKL1_000014 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) 0.00232 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 2024-08-28 13:16:32 +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.*9357A>C r.(=) p.(=)
MKL1 NM_020831.3 -/. - c.1322T>G r.(?) p.(Val441Gly)


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