Variant #0000528317 (NC_000006.11:g.31929014A>C, NM_006929.4:c.640A>C (SKIV2L))

Chromosome 6
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.31929014A>C
DNA change (hg38) g.31961237A>C
Published as SKIC2(NM_006929.5):c.640A>C (p.M214L)
ISCN -
DB-ID SKIV2L_000025
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) 0.76326 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NELFE NM_002904.5 -/. - c.-2354T>G r.(?) p.(=)
SKIV2L NM_006929.4 -/. - c.640A>C r.(?) p.(Met214Leu)


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