Variant #0000658963 (NC_000022.10:g.40814728C>T, NM_015705.4:c.*8965C>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.40814728C>T
DNA change (hg38) g.40418724C>T
Published as MRTFA(NM_001282662.2):c.2014G>A (p.G672S), MRTFA(NM_020831.6):c.2014G>A (p.G672S)
ISCN -
DB-ID MKL1_000022 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +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.*8965C>T r.(=) p.(=)
MKL1 NM_020831.3 ?/. - c.1714G>A r.(?) p.(Gly572Ser)


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