Variant #0000621467 (NC_000005.9:g.131671515_131671517del, NM_003060.3:c.-34150_-34148del (SLC22A5))

Chromosome 5
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.131671515_131671517del
DNA change (hg38) g.132335822_132335824del
Published as SLC22A4(NM_003059.3):c.1266_1268delTTA (p.Y423del)
ISCN -
DB-ID SLC22A4_000006
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 2019-12-06 12:43:26 +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     
SLC22A4 NM_003059.2 ?/. - c.1266_1268del r.(?) p.(Tyr423del)
SLC22A5 NM_003060.3 ?/. - c.-34150_-34148del r.(?) p.(=)


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