Variant #0000308463 (NC_000017.10:g.42336640_42336654del, NM_000342.3:c.760_774del (SLC4A1))

Chromosome 17
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.42336640_42336654del
DNA change (hg38) g.44259272_44259286del
Published as SLC4A1(NM_000342.3):c.760_774delGAGGCGGTGGAGCTG (p.E254_L258del)
ISCN -
DB-ID SLC4A1_000018
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 2018-01-15 20:58:59 +01:00 (CET)
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     
SLC4A1 NM_000342.3 ?/. - c.760_774del r.(?) p.(Glu254_Leu258del)


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