125946148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35429368-C-T

http://identifiers.org/hco/11/GRCh38#125946154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35429362-C-A

125946154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35429362-C-G

125946154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35429362-C-T

http://identifiers.org/hco/11/GRCh38#125946241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35429301-C-A

125946241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35429301-C-T

125946259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35429282-G-T

125947575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35428499-G-A

125947575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35428499-G-T

125947606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35428470-A-G

125947614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35428462-T-C

125947622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35428453-A-G

http://identifiers.org/hco/11/GRCh38#125947672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35428401-C-A

http://identifiers.org/hco/11/GRCh38#125947691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35428384-C-A

125947691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35428384-C-T

http://identifiers.org/hco/11/GRCh38#125947694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35428381-C-A

125947694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35428381-C-T

125947769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35428306-T-A

125947769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35428306-T-C

125947844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35428231-G-A

125947909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: synonymous variant
orthologous variants: 35428166-G-T

http://identifiers.org/hco/11/GRCh38#125947951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35428124-C-A

125948178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427891-A-T

125948186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427883-G-A

125948186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427883-G-T

125948193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427876-T-A

125948193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427876-T-C

125948211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427857-T-C

http://identifiers.org/hco/11/GRCh38#125948281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35427797-C-A

125948281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427797-C-T

125948282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427796-G-A

125948282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427796-G-C

125948282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427796-G-T

http://identifiers.org/hco/11/GRCh38#125948285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35427793-C-A

125948285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427793-C-T

125948300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 35427778-G-A

125948300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 35427778-G-T

125948437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35427641-G-A

125948437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35427641-G-T

http://identifiers.org/hco/11/GRCh38#125948439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35427639-C-A

125948439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35427639-C-G

125948439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35427639-C-T

125948646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427447-T-C

125948685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427408-G-A

125948729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427365-T-G

125948824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427278-A-G

125948872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35427230-C-T

125949205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35426893-G-C

125949382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35426604-G-A

125949382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35426604-G-T

125949406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35426584-C-T

125949717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35426269-G-C

125949758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35426205-A-G

http://identifiers.org/hco/11/GRCh38#125949944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35426012-C-A

125949947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35426009-A-G

125949947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35426009-A-T

http://identifiers.org/hco/11/GRCh38#125949954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35426002-C-A

125949954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35426002-C-T

125949956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35426000-T-C

125949961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425995-G-A

125949961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425995-G-T

http://identifiers.org/hco/11/GRCh38#125950154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35425802-C-A

125950154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35425802-C-G

125950269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35425687-C-T

125950301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425655-G-A

125950301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425655-G-C

125950301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425655-G-T

125950309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425647-G-A

125950309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425647-G-T

125950364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425616-T-C

125950378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425602-C-T

http://identifiers.org/hco/11/GRCh38#125950384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35425598-C-A

125950384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425598-C-T

125950414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35425574-G-C

125950956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35425129-G-T

125951003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35425082-A-G

125951050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35425035-A-T

125951074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35425011-G-A

125951074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35425011-G-T

125951143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense variant
orthologous variants: 35424942-T-C

125951192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35424892-A-G

125951199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35424885-G-A

125951199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35424885-G-T

125951226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35424860-A-G

125951294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35424798-G-T

125951520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35424607-C-T

http://identifiers.org/hco/11/GRCh38#125951654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35424470-C-A

125951667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35424457-A-G

125951700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35424420-A-G

125951759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron variant
orthologous variants: 35424395-C-T

125951795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35424361-A-T

125951807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35424350-T-A

125951807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35424350-T-C

http://identifiers.org/hco/11/GRCh38#125951862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35424295-C-A

125951892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35424265-T-C

125951908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35424249-G-C

125952039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35424121-C-T

125952157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35424009-T-C

125952157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35424009-T-G

125952266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35423875-T-C

125952266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35423875-T-G

125952301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35423840-T-C

125952429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35423736-A-G

125952474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35423694-G-T

125952771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35423379-T-C

125952974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35423196-G-A

125953056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35423136-G-T

125953317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422922-T-C

125953340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422883-G-A

125953340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422883-G-T

125953382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422836-T-C

http://identifiers.org/hco/11/GRCh38#125953427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35422791-C-A

125953427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35422791-C-G

125953427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35422791-C-T

125953483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35422735-G-A

125953574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35422644-C-T

125953593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35422625-C-T

125953697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35422518-G-T

125953779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422459-A-G

125953779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422459-A-T

125953837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422420-G-T

125953916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422342-T-C

http://identifiers.org/hco/11/GRCh38#125953967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35422299-C-A

125953967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422299-C-G

125953967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422299-C-T

125953977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422290-G-T

125953997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422274-G-A

125953997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422274-G-C

125953997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422274-G-T

125954069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422210-G-A

125954069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422210-G-C

125954069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35422210-G-T

http://identifiers.org/hco/11/GRCh38#125954104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35422175-A-C

125954104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35422175-A-G

125954164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35422115-G-A

125954237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35422042-G-A

125954237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35422042-G-T

125954283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35421996-A-G

125954411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35421867-A-G

125954456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35421818-A-G

125954479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35421797-T-C

125954788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35421516-A-G

125954948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35421355-G-T

125954995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35421322-G-T

http://identifiers.org/hco/11/GRCh38#125954997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35421320-C-A

http://identifiers.org/hco/11/GRCh38#125955048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35421270-C-A

125955048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35421270-C-T

125955167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35421151-G-A

125955167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 35421151-G-T

125955241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35421077-T-C

http://identifiers.org/hco/11/GRCh38#125955319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35421043-A-C

125955428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35420934-T-C

http://identifiers.org/hco/11/GRCh38#125955584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35420782-C-A

125955584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35420782-C-T

125955637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35420725-G-T

125955643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35420719-A-G

125955658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35420704-G-A

125955658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35420704-G-T

125955677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35420685-T-C

125955916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420496-G-A

http://identifiers.org/hco/11/GRCh38#125956003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35420346-C-A

125956003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420346-C-G

125956003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420346-C-T

125956034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420267-T-G

http://identifiers.org/hco/11/GRCh38#125956045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35420256-C-A

125956061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420240-A-G

125956087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420220-A-T

http://identifiers.org/hco/11/GRCh38#125956115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35420195-C-A

125956115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420195-C-T

125956146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420179-A-G

125956251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420075-G-A

125956251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420075-G-T

125956262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35420011-A-G

125956315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35419958-G-A

125956411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419879-T-C

125956495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419807-G-A

125956495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419807-G-T

125956502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419800-G-C

125956502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419800-G-T

http://identifiers.org/hco/11/GRCh38#125956767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35419591-C-A

http://identifiers.org/hco/11/GRCh38#125956799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35419559-A-C

125956799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419559-A-T

125956845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419511-T-A

125956845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419511-T-C

125956904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419453-G-T

http://identifiers.org/hco/11/GRCh38#125956943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35419414-C-A

125956943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419414-C-T

http://identifiers.org/hco/11/GRCh38#125956957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35419400-A-C

125956957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419400-A-G

http://identifiers.org/hco/11/GRCh38#125957013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#35419345-C-A

125957013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419345-C-T

125957065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419297-T-A

125957065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3 prime UTR variant
orthologous variants: 35419297-T-G

125957122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 35419243-C-G

125957122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 35419243-C-T

125957357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 35419061-A-G

125957358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 35419060-G-T

125957372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 35419046-G-A

125957372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 35419046-G-T

125957442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 35418951-G-T

http://identifiers.org/hco/11/GRCh38#125957501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#35418892-C-A

125957601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418791-A-G

125957690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418701-T-A

http://identifiers.org/hco/11/GRCh38#125957829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#35418582-C-A

125957829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418582-C-G

125957872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418538-A-G

125957983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418446-T-C

125958027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418381-G-T

125958096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418309-C-G

125958185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418248-C-T

125958202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418233-A-G

125958244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418201-A-G

125958252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418193-G-A

125958252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418193-G-T

http://identifiers.org/hco/11/GRCh38#125958277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#35418169-C-A

125958297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418151-G-A

125958297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35418151-G-T

http://identifiers.org/hco/11/GRCh38#125958434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#35418013-A-C

http://identifiers.org/hco/11/GRCh38#125958461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#35417986-C-A

125958461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27879
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35417986-C-T