Variant #0000543936 (NC_000011.9:g.45827855_45827857del, NM_018389.4:c.503_505del (SLC35C1))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45827855_45827857del
DNA change (hg38) g.45806304_45806306del
Published as SLC35C1(NM_001145265.1):c.464_466del (p.(Phe155del)), SLC35C1(NM_018389.4):c.503_505delTCT (p.F168del), SLC35C1(NM_018389.5):c.503_505delTCT (p.F1...)
ISCN -
DB-ID SLC35C1_000005 See all 3 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_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 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC35C1 NM_018389.4 +/. - c.503_505del r.(?) p.(Phe168del)


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