243917426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 177150446-G-C

243917426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 177150446-G-T

243917571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177150589-G-A

243917571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177150589-G-T

http://identifiers.org/hco/1/GRCh38#243917616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#177150633-C-A

243917616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177150633-C-T

243917655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177150672-G-A

243917676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177150693-C-T

243917795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177150823-C-T

243918056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177151123-C-T

243918115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177151180-T-C

243918152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177151222-G-A

243918531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177151720-T-C

243918681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177151832-C-T

243920030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177152377-A-T

243920053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177152397-G-C

http://identifiers.org/hco/1/GRCh38#243920186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177152730-C-A

243920632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177153488-C-G

243920663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177153526-C-G

243920692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177153552-C-G

243920698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177153561-A-G

243920753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177153620-C-T

243920761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177153626-G-A

243920788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177153648-C-G

243920788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177153648-C-T

243924876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177159318-T-C

243924876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177159318-T-G

243925305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177159664-G-A

243925321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177159680-A-G

243925368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177159726-C-T

243925459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177159820-T-C

243926082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177160328-T-A

243926129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177160377-G-A

243926154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177160401-C-T

243926351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177160707-C-G

243926514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177160865-G-T

243926569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177160995-G-C

243926754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177161413-A-G

http://identifiers.org/hco/1/GRCh38#243926757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177161416-A-C

243926757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177161416-A-G

243926906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177161557-C-T

243926913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177161564-A-G

243927322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177161961-G-A

243927372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177162010-C-T

243927609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177162265-G-A

243927866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177162523-T-G

243927925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177162582-A-G

243928066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177163038-A-G

243928346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177163320-C-T

243928395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177163368-G-A

243929583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177165100-G-A

243929782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177165410-C-T

243929956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177165585-T-C

243930218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177165740-G-T

243930235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177165757-A-G

243931063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177166296-A-G

243931182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177166414-C-G

243931336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177166565-A-G

243932717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177167779-A-G

243932807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177167875-T-C

243932807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177167875-T-G

243933275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177168297-G-T

243933380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177168374-A-G

243933399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177168391-C-T

243933405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177168397-C-G

243933405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177168397-C-T

http://identifiers.org/hco/1/GRCh38#243933606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177168742-C-A

243935444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177170233-C-G

243935641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177170405-G-T

http://identifiers.org/hco/1/GRCh38#243935785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177170533-A-C

243936119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177170860-C-T

http://identifiers.org/hco/1/GRCh38#243936124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177170865-A-C

243936124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177170865-A-G

243936322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177171065-C-T

243936374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177171090-C-G

243936388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177171104-G-A

243937082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177171496-G-A

243939016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177171863-G-T

243939411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177172226-T-G

http://identifiers.org/hco/1/GRCh38#243939413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177172228-A-C

243939413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177172228-A-T

243939880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177173204-G-A

243940165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177173480-A-G

243941345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177174196-A-G

243941370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177174221-G-A

243941429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177174273-C-T

243942296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177174901-T-A

243942617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177175240-T-C

243942758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177175626-G-A

http://identifiers.org/hco/1/GRCh38#243942811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177175676-C-A

243943080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177175913-G-A

243943118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177175951-G-T

243943187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177176023-T-C

http://identifiers.org/hco/1/GRCh38#243943727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177176498-C-A

243943931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177176863-G-A

243944663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177177477-C-G

243944663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177177477-C-T

243944704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177177525-G-A

243944704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177177525-G-T

243944731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177177554-T-C

243944779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177177595-A-G

243944983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177177795-C-G

243944983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177177795-C-T

243945564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177178056-A-G

243946346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177178532-A-G

243946401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177178587-T-G

243947150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177179430-G-T

243947164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177179480-G-A

243947164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177179480-G-T

243947282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177179622-C-G

243947484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177179800-G-A

243947670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177179970-G-A

243948919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177181853-C-T

http://identifiers.org/hco/1/GRCh38#243948954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177181889-C-A

243948976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177181908-G-A

243950272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177182736-C-T

243950298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177182761-G-T

http://identifiers.org/hco/1/GRCh38#243950461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177182923-A-C

243950476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177182938-C-T

243950479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177182943-C-T

243950480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177182944-T-C

243950481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177182945-G-T

243950495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177182959-T-C

243950499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177182963-G-C

243950578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177183043-C-T

http://identifiers.org/hco/1/GRCh38#243950882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177183453-C-A

243951000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177183775-G-A

243951000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177183775-G-T

243951117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177183891-A-G

243954672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177185504-A-G

243954967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177185769-G-A

243954973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177185775-G-A

243955042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177185844-C-T

243955156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177185966-G-A

243956302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177187256-A-G

243956736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177188191-C-T

243956774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177188210-C-T

243957576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177190124-A-G

243957577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177190125-C-T

243957760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177190306-G-A

243957881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177190428-T-C

243958030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177190573-T-C

243958030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177190573-T-G

243958041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177190580-G-T

243959309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177191176-A-G

243959957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177191847-T-C

243959957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177191847-T-G

243960918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177192833-T-A

243960918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177192833-T-C

243961434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177193770-T-C

243962658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177195021-C-G

243964038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177198865-T-G

243964174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177198993-G-A

243964201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177199020-G-T

243964392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177199206-T-C

243964806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177199259-G-A

243964813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177199266-A-G

243964904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177199360-C-T

243964979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177199463-A-T

243964996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177199501-A-T

243965779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177199682-A-G

http://identifiers.org/hco/1/GRCh38#243965972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177199864-A-C

243966185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177200065-C-T

http://identifiers.org/hco/1/GRCh38#243966231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177200113-A-C

243966326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177200189-A-T

243966612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177200467-A-G

243966873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177200713-G-A

243967335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177200895-A-G

243967418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177200978-C-T

243968029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177201628-A-G

http://identifiers.org/hco/1/GRCh38#243968349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177201942-A-C

243968355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177201948-A-G

243968523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177204380-A-T

http://identifiers.org/hco/1/GRCh38#243968557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177204404-A-C

243968578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177204425-T-A

243968595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177204442-A-G

243968597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177204444-G-A

243968882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177204651-T-C

243968897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177204666-A-G

243968947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177204719-G-C

243968954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177204726-C-T

243969079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177204844-A-G

243969110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177204875-G-A

243969403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177205184-G-A

243970166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206103-T-C

243970189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206126-G-A

243970216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206154-A-G

243970296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206232-G-A

243970343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206277-G-A

243970375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206306-C-T

243970390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206321-G-A

http://identifiers.org/hco/1/GRCh38#243970499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177206427-A-C

243970499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206427-A-T

243970518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206449-C-T

243970526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206457-A-G

243970527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206458-G-T

243970528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206459-A-T

243970864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177206822-A-G

http://identifiers.org/hco/1/GRCh38#243970886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177206844-C-A

243971129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177207017-T-A

243971251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177207101-T-G

243971263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177207113-A-G

http://identifiers.org/hco/1/GRCh38#243971377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177207224-A-C

243971377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177207224-A-G

243971640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177207532-C-T

243972746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177207735-A-G

243972773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177207760-C-T

243973115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177208264-A-T

http://identifiers.org/hco/1/GRCh38#243973244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177208359-C-A

http://identifiers.org/hco/1/GRCh38#243973324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177208437-C-A

243973415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177208515-G-A

243973423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177208523-T-G

http://identifiers.org/hco/1/GRCh38#243973495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177208596-C-A

http://identifiers.org/hco/1/GRCh38#243973763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177209492-A-C

243973763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177209492-A-G

243973919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177209637-T-C

243973985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177209704-T-A

243973985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177209704-T-C

243974229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177209944-T-A

243974229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177209944-T-C

243974269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177209978-A-G

243974748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177210463-G-A

243974869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177210581-C-G

243974980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 177210689-A-T

http://identifiers.org/hco/1/GRCh38#243975166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177210836-C-A

243975166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177210836-C-T

243975171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177210841-G-C

243975171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177210841-G-T

243975230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177210875-G-A

243975567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177211179-T-C

243975728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177211315-T-A

http://identifiers.org/hco/1/GRCh38#243977358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177211869-C-A

243977358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177211869-C-T

243977404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177211915-C-T

243977883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177212344-G-A

243977939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177212400-A-G

243978051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177212497-G-A

243978246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177212681-G-A

243978246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177212681-G-C

243978276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177212712-G-A

243978356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177212787-C-G

243978401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177212842-T-G

243982448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177213611-T-C

243982601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177213805-G-A

http://identifiers.org/hco/1/GRCh38#243982745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177213935-C-A

243982745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177213935-C-G

243982821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177214008-G-C

243983166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177218126-C-T

243983763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177218895-T-A

243984476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177219038-G-A

243984750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177219567-G-T

243984868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177219663-G-A

243984868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177219663-G-C

243988057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177221853-G-A

243988180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177221969-C-G

243988361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177222159-G-A

243993220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177223505-A-G

243993235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177223520-A-G

243993324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177223601-C-T

243993417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177223638-T-C

243993581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177223798-C-T

243993586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177223803-G-T

243993687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177223890-G-A

243995371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177226553-A-T

243995416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177226572-T-C

243995470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177226634-G-A

243995522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177226680-C-T

243995809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177226879-G-A

243995831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177226922-G-T

243996384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177227179-C-T

243996434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177227233-C-G

243996667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177227467-A-G

243996689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177227487-A-G

243996902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177227737-T-A

243996902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177227737-T-C

243997005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177227827-T-C

243998971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177228368-T-C

243998977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177228374-C-T

http://identifiers.org/hco/1/GRCh38#243999024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177228420-A-C

243999200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177228631-T-C

244001444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177232030-C-T

http://identifiers.org/hco/1/GRCh38#244001815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177232326-A-C

http://identifiers.org/hco/1/GRCh38#244010599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177237784-C-A

244010599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177237784-C-T

http://identifiers.org/hco/1/GRCh38#244010694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177237872-C-A

244010694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 177237872-C-T

http://identifiers.org/hco/1/GRCh38#244010783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177237957-C-A

244010838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: 177238007-A-G

244010891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: 177238052-T-A

244011147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238294-C-T

244011236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238380-T-C

http://identifiers.org/hco/1/GRCh38#244011268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177238401-A-C

244011268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238401-A-T

http://identifiers.org/hco/1/GRCh38#244011269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177238402-C-A

244011269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238402-C-T

244011272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238405-T-G

244011279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238412-T-C

244011281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238414-C-T

http://identifiers.org/hco/1/GRCh38#244011320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177238436-C-A

244011349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238465-G-A

244011349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238465-G-T

244011834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238942-C-T

244011866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177238986-A-G

244012469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177239515-G-C

244013008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177240054-A-G

244018787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177242828-G-C

244018814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177242855-G-A

244018825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177242872-G-A

244021160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177243934-C-T

http://identifiers.org/hco/1/GRCh38#244021207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177243981-C-A

244021425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177244194-A-G

244021425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177244194-A-T

244021529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177244300-C-G

244021559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177244334-G-A

http://identifiers.org/hco/1/GRCh38#244021762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177244505-C-A

244025996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177244817-G-C

244026149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177244967-A-G

244026482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177245412-G-T

244027018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177245963-C-G

244027270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: 177246257-T-C

244027281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: 177246268-A-G

244027284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: 177246269-G-A

244027317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: 177246301-A-G

http://identifiers.org/hco/1/GRCh38#244027410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177246393-C-A

244027428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: 177246411-G-A

http://identifiers.org/hco/1/GRCh38#244027437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177246419-A-C

244027437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177246419-A-G

http://identifiers.org/hco/1/GRCh38#244027470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177246444-A-C

244027470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177246444-A-G

244027540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177246499-G-C

http://identifiers.org/hco/1/GRCh38#244027564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177246521-A-C

244027754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177246715-T-G

244027995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177246910-G-A

244028039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177246954-T-A

244028061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177246976-C-T

244028560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177247174-A-G

244028608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177247219-C-G

http://identifiers.org/hco/1/GRCh38#244028609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177247220-A-C

http://identifiers.org/hco/1/GRCh38#244028632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177247243-A-C

244028686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177247288-G-T

244028730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177247332-T-C

244029089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177247670-A-G

244029099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177247680-G-A

244029321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177247895-C-T

244029455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177248034-T-C

244029668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177248250-T-C

244030490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177250013-G-A

244030778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177250324-T-C

244030937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177250483-C-G

244030951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177250497-G-A

244031126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177250664-T-G

244031550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177251450-T-G

http://identifiers.org/hco/1/GRCh38#244031644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177251540-A-C

244031764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177251779-A-G

244032533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177251892-A-G

244032537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177251896-G-A

244033782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177254267-C-T

244034179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177254655-C-T

244034241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177254820-C-T

244035598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177254972-C-G

244035598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177254972-C-T

244035807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177255174-G-A

244035807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177255174-G-C

http://identifiers.org/hco/1/GRCh38#244035857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177255225-C-A

244035902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177255267-A-G

244036079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177255383-A-G

244036592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177255777-A-G

244036625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177255808-T-C

244036695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177255875-T-G

244036753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177255943-T-C

244037099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177256290-A-G

244037131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177256322-T-C

http://identifiers.org/hco/1/GRCh38#244037229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177256440-C-A

244037381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177256624-G-A

244037424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177256645-G-A

http://identifiers.org/hco/1/GRCh38#244038402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177257651-C-A

244038402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177257651-C-T

244039092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177258519-G-T

244039272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177258698-G-C

244039617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177259346-T-A

244039648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177259377-G-A

244040018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177259804-C-T

244040107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177259891-C-G

244040274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177260057-T-C

244040378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177260161-G-A

244040548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177260332-G-A

244040786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177260545-C-T

244041032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177260894-G-A

244041263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177261697-A-G

244041286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177261721-C-T

http://identifiers.org/hco/1/GRCh38#244041407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177261767-C-A

244041697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177262581-G-A

244041697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177262581-G-T

244041708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177262590-G-T

244041712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177262594-G-A

244041802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177262682-A-G

244042322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177262987-G-C

http://identifiers.org/hco/1/GRCh38#244042398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177263052-C-A

244042607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177263370-T-C

244042705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177263527-C-T

244043300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177264069-G-A

244043300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177264069-G-C

244043575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177264359-T-C

244044021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177264856-C-T

244044420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177265318-T-C

244045134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177266304-C-T

244045218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177266383-T-C

http://identifiers.org/hco/1/GRCh38#244045317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177266537-C-A

244045317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177266537-C-T

244045535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177266856-T-G

244045591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 177266895-A-T

244045805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177267072-T-A

244046097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177267353-G-A

244046160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177267416-A-G

244046332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177267546-A-T

244046616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177267822-G-A

244046616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177267822-G-T

244046626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177267832-T-C

244046846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177268083-T-C

244046851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 177268088-A-G

244047068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: 177268480-T-C

http://identifiers.org/hco/1/GRCh38#244047070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#177268482-C-A

244047070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: 177268482-C-T

244047117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27923
most severe consequence: non coding transcript exon variant
orthologous variants: 177268527-G-T