http://identifiers.org/hco/5/GRCh38#127517657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57487847-A-C

http://identifiers.org/hco/5/GRCh38#127517730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57487917-C-A

127517809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57487988-G-T

127517897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488039-G-A

127517963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57488054-C-T

http://identifiers.org/hco/5/GRCh38#127517994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57488087-C-A

127517994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57488087-C-T

127518111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488153-A-G

127518307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488262-C-T

127518325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488278-G-A

127518869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57488958-G-A

127518902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57489001-C-T

127519163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57489254-T-C

127519219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57489311-T-G

127519276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57489362-G-T

127519372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57489450-A-G

127519664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57489693-T-C

127519936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57489950-A-G

127520166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57490171-T-G

127520350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57490364-T-A

127520509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57490577-A-T

127520759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57490801-A-G

127520996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57491012-G-A

127521007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57491019-T-C

127522296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57494626-C-G

127522314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57494644-A-T

127522363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57494684-G-A

127522405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57494725-T-C

127523384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57495440-G-A

127523384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57495440-G-T

127523393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57495449-T-C

127523395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57495451-T-G

http://identifiers.org/hco/5/GRCh38#127523397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57495453-C-A

127523397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57495453-C-T

127523411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57495458-A-G

127523411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57495458-A-T

127523444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57495489-T-G

127523463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57495508-A-G

127523463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57495508-A-T

127523466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 57495511-A-G

127523512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57495557-A-G

http://identifiers.org/hco/5/GRCh38#127523599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57495629-A-C

127523599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495629-A-G

127523602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495632-A-G

127523647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495661-A-G

127523647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495661-A-T

127523694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495700-T-A

127523694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495700-T-C

127523703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495709-G-T

127523719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495726-T-C

127523719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495726-T-G

127523720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495727-T-A

127523720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495727-T-G

127523725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495732-T-C

127523725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495732-T-G

127523734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495741-A-G

http://identifiers.org/hco/5/GRCh38#127523752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57495766-A-C

http://identifiers.org/hco/5/GRCh38#127523856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57495823-A-C

127523856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57495823-A-G

http://identifiers.org/hco/5/GRCh38#127524216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57495877-C-A

127524216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57495877-C-T

127524233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57495894-T-C

127524257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57495918-G-A

127524257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57495918-G-T

http://identifiers.org/hco/5/GRCh38#127524258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57495919-C-A

127524258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57495919-C-T

127524412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496038-T-C

127524418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496044-G-C

127524418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496044-G-T

127524457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496083-G-A

127524457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496083-G-C

127524457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496083-G-T

http://identifiers.org/hco/5/GRCh38#127524489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57496106-C-A

127524489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496106-C-T

127524490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496107-A-G

http://identifiers.org/hco/5/GRCh38#127524534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57496151-C-A

127524534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense variant
orthologous variants: 57496151-C-T

http://identifiers.org/hco/5/GRCh38#127524565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57496182-C-A

127524578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense variant
orthologous variants: 57496195-T-C

127524590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense variant
orthologous variants: 57496207-G-A

127524590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense variant
orthologous variants: 57496207-G-T

http://identifiers.org/hco/5/GRCh38#127524591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57496208-C-A

127524673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: synonymous variant
orthologous variants: 57496290-T-G

127524701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense variant
orthologous variants: 57496318-C-T

http://identifiers.org/hco/5/GRCh38#127524927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57496545-C-A

127524930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496548-T-C

127524949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496569-T-A

127524964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496580-G-A

127524964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496580-G-T

127525636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496689-C-T

127525775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496818-G-A

127525911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57496992-G-A

127526008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57497058-T-C

http://identifiers.org/hco/5/GRCh38#127526115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57497160-C-A

127526453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498098-A-G

127526461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498106-T-C

127526467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498112-G-T

127526585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498230-A-G

127526609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498252-A-G

127526682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: synonymous variant
orthologous variants: 57498325-C-T

127526757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: synonymous variant
orthologous variants: 57498400-T-A

127526757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: synonymous variant
orthologous variants: 57498400-T-C

http://identifiers.org/hco/5/GRCh38#127526819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57498460-A-C

127526819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498460-A-G

127526825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498466-A-G

127526828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498469-A-G

127526879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498520-A-G

http://identifiers.org/hco/5/GRCh38#127526913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57498550-C-A

127526913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498550-C-T

127526934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57498588-A-G

127530231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504381-T-A

127530231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504381-T-C

127530308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense variant
orthologous variants: 57504453-T-A

127530407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504552-A-G

127530418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504562-G-A

127530423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504567-T-C

127530467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504607-T-A

127530467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504607-T-C

http://identifiers.org/hco/5/GRCh38#127530517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57504652-A-C

127530540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504675-T-C

127530662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504781-T-A

127530663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504782-T-A

127530699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57504804-A-G

127530942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57505037-A-G

127531022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57505130-A-G

127531149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57505252-G-A

127531292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57505399-A-T

http://identifiers.org/hco/5/GRCh38#127531418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57505662-A-C

127531510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57505788-C-T

http://identifiers.org/hco/5/GRCh38#127531532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57505810-A-C

127531535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57505813-A-G

127531582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57505842-C-G

127533560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57507522-G-A

127533560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57507522-G-T

127533822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57507791-C-T

http://identifiers.org/hco/5/GRCh38#127533924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57507863-C-A

127533924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57507863-C-T

http://identifiers.org/hco/5/GRCh38#127533967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57507907-A-C

127533968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57507908-A-G

127533992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57507943-T-C

127534008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57507972-A-G

127534293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57508243-A-G

127534383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57509263-G-A

127534524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57509494-A-G

127534582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57509555-T-G

127534585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57509558-G-A

http://identifiers.org/hco/5/GRCh38#127534754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57509730-A-C

127534790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57509764-G-A

127534932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57509931-G-C

127535279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57510270-G-A

127535279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57510270-G-C

127535343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57510338-C-T

127535409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57510530-A-G

127535490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57510642-T-A

127535536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57510689-A-G

127535604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57510764-G-A

127535727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57510853-C-T

127536006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57511066-G-A

127536104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57511150-T-C

127536443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57511441-T-A

127536443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57511441-T-C

127536443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57511441-T-G

127536716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57512043-A-G

127536944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57512239-T-G

127537225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57512630-G-T

127537398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57512796-G-C

127537401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57512799-G-A

127537502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57512904-A-G

127537515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57512917-T-A

127537592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57512986-G-T

127537665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57513048-C-T

http://identifiers.org/hco/5/GRCh38#127537730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57513107-A-C

127537775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57513154-A-G

127537831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57513208-G-A

127537903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57513272-T-C

127538089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57513428-T-C

127538106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57513441-C-T

127538303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57513775-T-A

127538321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57513796-C-G

127538509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57513974-G-A

127538565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514030-G-A

127538707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514167-C-T

127538776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514225-T-C

127538854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514439-G-A

127538900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514578-T-G

127538904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514582-G-C

127538904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514582-G-T

127538954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514616-G-A

127538954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514616-G-T

127539042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 57514702-T-C

127539067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense variant
orthologous variants: 57514727-C-G

127539067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense variant
orthologous variants: 57514727-C-T

127539099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: synonymous variant
orthologous variants: 57514759-A-G

127539163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514823-C-T

127539164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514824-T-C

127539176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514834-T-C

127539178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514836-T-C

127539178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514836-T-G

127539185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514843-G-A

127539223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514868-T-C

127539239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514885-G-C

127539255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514901-T-C

http://identifiers.org/hco/5/GRCh38#127539291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57514912-C-A

127539291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514912-C-G

127539315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57514936-A-G

127539399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57515020-T-C

127539404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57515025-A-G

127539540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57515144-G-A

127539540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57515144-G-C

127539688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57515309-T-C

http://identifiers.org/hco/5/GRCh38#127546849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57516075-C-A

127546858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516084-T-G

http://identifiers.org/hco/5/GRCh38#127546885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57516108-C-A

127546885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516108-C-T

127546904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516127-T-C

127547046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516263-C-T

127547094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516314-C-T

127547261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516465-T-G

127547297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516501-C-T

127547391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516595-T-G

127547464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516663-A-G

127547491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516689-T-A

127547491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516689-T-G

127547493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516701-C-T

127547494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516702-A-G

127547552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516949-C-T

127547577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57516986-T-C

127547657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57517067-T-G

127547680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57517089-T-C

http://identifiers.org/hco/5/GRCh38#127547708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57517106-C-A

127547708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57517106-C-T

127547715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57517113-A-G

127547730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57517128-G-A

127547730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57517128-G-T

127547756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57517184-T-C

127547806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron variant
orthologous variants: 57517233-A-G

127547852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57517279-T-A

http://identifiers.org/hco/5/GRCh38#127548034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57517410-A-C

127548038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57517414-A-G

127548068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57517427-T-A

127548068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57517427-T-C

http://identifiers.org/hco/5/GRCh38#127548107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57517461-C-A

127548389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519048-A-G

127548389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519048-A-T

127548414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519071-G-C

127548414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519071-G-T

http://identifiers.org/hco/5/GRCh38#127548454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57519084-C-A

127548454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519084-C-T

127548474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519104-T-G

127548475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519105-G-T

http://identifiers.org/hco/5/GRCh38#127548514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57519145-A-C

127548514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519145-A-T

http://identifiers.org/hco/5/GRCh38#127548643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57519184-C-A

127548710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519248-A-G

127548712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519250-G-A

127548714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519252-G-A

127548714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519252-G-C

127548714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519252-G-T

http://identifiers.org/hco/5/GRCh38#127548761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57519294-C-A

127548761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519294-C-T

127549036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519484-A-G

127549192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519631-C-T

127549552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519943-C-T

127549587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519979-C-G

127549587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57519979-C-T

127549675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520066-C-G

http://identifiers.org/hco/5/GRCh38#127549789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57520179-A-C

127549789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520179-A-G

http://identifiers.org/hco/5/GRCh38#127549794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57520184-C-A

127549958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520319-A-G

127550072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520427-T-C

127550078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520433-T-A

127550108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520454-G-T

127550111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520457-A-G

127550124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520464-A-G

127550146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520486-A-G

127550192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520517-T-G

127550194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520519-T-C

127550410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520904-A-G

127550410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57520904-A-T

127550484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521074-G-A

127550494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521084-C-T

127550538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521128-A-G

http://identifiers.org/hco/5/GRCh38#127550611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57521193-C-A

127550611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521193-C-T

127550613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521204-G-A

127550622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521213-G-A

127550688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521279-T-G

http://identifiers.org/hco/5/GRCh38#127550809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57521343-C-A

127550829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521356-G-A

127550829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521356-G-C

127550835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521362-G-A

127550837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521364-C-T

127550839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521366-G-A

127550908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521431-G-C

127550908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521431-G-T

127551010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521532-T-C

http://identifiers.org/hco/5/GRCh38#127551163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57521646-C-A

127551163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521646-C-T

127551280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521772-G-A

http://identifiers.org/hco/5/GRCh38#127551306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57521803-C-A

http://identifiers.org/hco/5/GRCh38#127551397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57521892-C-A

127551397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57521892-C-T

127551505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57522084-T-C

127551513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57522092-T-C

127551547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57522123-G-T

127551637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57522220-G-A

127551637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57522220-G-T

127551647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57522230-G-C

127551674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57522260-A-G

127551938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522519-T-G

127552007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522573-A-G

127552084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522669-A-G

127552142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522727-A-G

127552158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522740-A-G

127552158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522740-A-T

127552171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522753-C-T

127552181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522763-T-C

127552188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522770-G-A

127552188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522770-G-T

127552254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522831-T-A

127552254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522831-T-C

127552335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522870-G-A

127552335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522870-G-T

127552426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522946-G-A

127552426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57522946-G-T

127552505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523019-A-G

127552510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523024-G-A

127552510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523024-G-C

127552518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523032-G-A

127552540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523053-T-C

127552562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523074-T-A

127552562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523074-T-C

127552611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523124-T-C

127552611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523124-T-G

127552686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523209-G-A

127552686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523209-G-C

127552686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523209-G-T

http://identifiers.org/hco/5/GRCh38#127552934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57523956-C-A

127552992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57523984-T-C

127553048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524041-T-A

127553048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524041-T-C

127553048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524041-T-G

http://identifiers.org/hco/5/GRCh38#127553054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57524046-C-A

127553107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524099-A-G

127553107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524099-A-T

127553182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524153-G-C

http://identifiers.org/hco/5/GRCh38#127553284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57524234-C-A

127553321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524260-T-A

127553341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524278-T-C

127553342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524279-A-G

127553343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524280-T-C

127553380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524322-A-T

http://identifiers.org/hco/5/GRCh38#127553726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57524719-C-A

127553726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524719-C-T

127553739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524732-T-G

127553784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 57524782-G-A

127553795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, splice_acceptor_variant
orthologous variants: 57524793-A-G

http://identifiers.org/hco/5/GRCh38#127553803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57524801-A-C

127554012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57524973-G-A

127554012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57524973-G-T

127554017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57524978-T-C

127554058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525016-T-C

127554101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525058-A-G

127554203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525135-T-C

http://identifiers.org/hco/5/GRCh38#127554261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57525191-C-A

127554262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525192-T-C

127554265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525195-T-C

127554285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525219-G-T

127554289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525223-G-A

127554289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525223-G-T

127554342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525272-G-T

127554378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525319-T-A

127554378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525319-T-C

127554518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525435-A-G

http://identifiers.org/hco/5/GRCh38#127554577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#57525520-C-A

127554622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525606-A-G

127554768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525695-G-C

127554768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525695-G-T

127554942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525882-A-G

127554985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525925-T-C

127555011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28164
most severe consequence: 3 prime UTR variant
orthologous variants: 57525951-G-T