RGD:150411036 Rat Genome Database

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Variant: RGD:150411036 -  Homo sapiens

RGD ID: 150411036
RS ID: rs782081123
ClinVar ID: CV1196293
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TMEM255A  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 119,419,061
GRCh38 X 120,285,206
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001104544.3:c.433C>T
NC_000023.11:g.120285206G>A
NM_001104545.2:c.423+1948C>T
NC_000023.10:g.119419061G>A
More...
intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TMEM255A
Accession:XM_017029619
Location:EXON
Amino Acid Prediction: P to S (nonsynonymous)
Amino Acid Position: 169
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MHQSLTQQRSSDMSLPDSMGAFNRRKRNSIYVTVTLLIVSVLILTVGLAATTRTQNVTVGGYYPGVILGFGSFLGIIGSN
LIENKRQMLVASIVFISFGVIAAFCCAIVDGVFAARHIDLKPLYANRCHYVPKTSQKEAEEVISSSTKNSPSTRVMRNLT
QAAREVNCSHLSREFCTPRIRGNTCFCCDLYNCGNRVEITGGYYEYIDVSSCQDIIHLYHLLWSATILNIVGLFLGIITA
AVLGGFKDMNPTLPALNCSVENTHPTVSYYAHPQVASYNTYYHSPPHLPPYSAYDFQGGPRDSTSRSEPTPKICDSTVEK
PFHITVKPLTEGQFGGAGDGGKR*

Gene Symbol:TMEM255A
Accession:XM_047442232
Location:EXON
Amino Acid Prediction: P to S (nonsynonymous)
Amino Acid Position: 145
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MHQSLTQQRSSDMSLPDSMGAFNRRKRNSIYVTVTLLIVSVLILTVGLAATTRTQNVTVGGYYPGVILGFGSFLGIIGSN
LIENKRQMLVASIVFISFGVIAAFCCAIVDGVFAARHIDLKPLYANRCHYVPKTSQKEAEEVNCSHLSREFCTPRIRGNT
CFCCDLYNCGKTQLSQH*

Gene Symbol:TMEM255A
Accession:XM_047442231
Location:EXON
Amino Acid Prediction: P to S (nonsynonymous)
Amino Acid Position: 169
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MHQSLTQQRSSDMSLPDSMGAFNRRKRNSIYVTVTLLIVSVLILTVGLAATTRTQNVTVGGYYPGVILGFGSFLGIIGSN
LIENKRQMLVASIVFISFGVIAAFCCAIVDGVFAARHIDLKPLYANRCHYVPKTSQKEAEEVISSSTKNSPSTRVMRNLT
QAAREVNCSHLSREFCTPRIRGNTCFCCDLYNCGKTQLSQH*

Gene Symbol:TMEM255A
Accession:NM_017938
Location:EXON
Amino Acid Prediction: P to S (nonsynonymous)
Amino Acid Position: 169
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MHQSLTQQRSSDMSLPDSMGAFNRRKRNSIYVTVTLLIVSVLILTVGLAATTRTQNVTVGGYYPGVILGFGSFLGIIGSN
LIENKRQMLVASIVFISFGVIAAFCCAIVDGVFAARHIDLKPLYANRCHYVPKTSQKEAEEVISSSTKNSPSTRVMRNLT
QAAREVNCSHLSREFCTPRIRGNTCFCCDLYNCGNRVEITGGYYEYIDVSSCQDIIHLYHLLWSATILNIVGLFLGIITA
AVLGGFKDMNPTLPALNCSVENTHPTVSYYAHPQVASYNTYYHSPPHLPPYSAYDFQHSGVFPSSPPSGLSDEPQSASPS
PSYMWSSSAPPRYSPPYYPPFEKPPPYSP*

Gene Symbol:TMEM255A
Accession:NM_001104544
Location:EXON
Amino Acid Prediction: P to S (nonsynonymous)
Amino Acid Position: 145
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MHQSLTQQRSSDMSLPDSMGAFNRRKRNSIYVTVTLLIVSVLILTVGLAATTRTQNVTVGGYYPGVILGFGSFLGIIGSN
LIENKRQMLVASIVFISFGVIAAFCCAIVDGVFAARHIDLKPLYANRCHYVPKTSQKEAEEVNCSHLSREFCTPRIRGNT
CFCCDLYNCGNRVEITGGYYEYIDVSSCQDIIHLYHLLWSATILNIVGLFLGIITAAVLGGFKDMNPTLPALNCSVENTH
PTVSYYAHPQVASYNTYYHSPPHLPPYSAYDFQHSGVFPSSPPSGLSDEPQSASPSPSYMWSSSAPPRYSPPYYPPFEKP
PPYSP*

Gene Symbol:TMEM255A
Accession:NM_001104545
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001573445 CLINVAR
dbSNP (RS) rs782081123 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TMEM255A CLINVAR