94703826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118464620-C-G

94703942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118464732-G-A

94704041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118464884-C-T

94704090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118464935-G-T

94704169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118465014-G-T

94704514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118465415-G-C

94704853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118465749-A-T

94704871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118465761-G-A

94704877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118465766-G-T

94704960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118465848-G-A

94705613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118466500-G-T

94705787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118466764-A-G

94705964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118466977-C-T

94706241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118467265-T-C

94706244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118467268-C-T

94706245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118467269-G-A

94706248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118467272-T-C

94706286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118467309-C-T

94706590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118467636-C-T

94707206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118468265-A-G

94707449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118468509-G-A

94707463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118468523-T-C

94707619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118468671-C-T

94707731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118468790-C-T

http://identifiers.org/hco/13/GRCh38#94708174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118469198-A-C

http://identifiers.org/hco/13/GRCh38#94708387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118469399-C-A

94709122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118470141-G-A

94709198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118470217-C-T

http://identifiers.org/hco/13/GRCh38#94709249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118470268-C-A

94710270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118471309-T-C

94710308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118471347-G-T

94710477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118471499-G-A

94710756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118471790-G-A

94710756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118471790-G-T

http://identifiers.org/hco/13/GRCh38#94710877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118471882-C-A

94710877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118471882-C-T

94711145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472156-G-A

94711145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472156-G-T

94711146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472157-G-A

94711146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472157-G-T

http://identifiers.org/hco/13/GRCh38#94711324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118472322-C-A

94711324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472322-C-T

http://identifiers.org/hco/13/GRCh38#94711354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118472352-C-A

94711354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472352-C-T

http://identifiers.org/hco/13/GRCh38#94711363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118472361-C-A

94711363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472361-C-G

94711363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472361-C-T

http://identifiers.org/hco/13/GRCh38#94711390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118472388-C-A

94711390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472388-C-G

94711390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472388-C-T

94711429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472427-G-A

94711429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472427-G-T

94711447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472445-G-A

94711447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472445-G-C

94711447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472445-G-T

http://identifiers.org/hco/13/GRCh38#94711498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118472496-C-A

94711498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472496-C-G

94711498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472496-C-T

http://identifiers.org/hco/13/GRCh38#94711552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118472550-C-A

94711552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472550-C-G

94711552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472550-C-T

94711652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472650-T-C

94711652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472650-T-G

http://identifiers.org/hco/13/GRCh38#94711672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118472670-C-A

94711672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472670-C-G

94711804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472802-C-T

94711915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472913-C-G

94711915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118472913-C-T

http://identifiers.org/hco/13/GRCh38#94712427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118473427-C-A

http://identifiers.org/hco/13/GRCh38#94712437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118473437-C-A

94712459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118473459-T-C

94712488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118473488-G-C

http://identifiers.org/hco/13/GRCh38#94712489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118473489-A-C

94712489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118473489-A-G

94712615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118473608-G-T

94712668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118473641-G-A

94712668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118473641-G-T

94712730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118473700-G-T

http://identifiers.org/hco/13/GRCh38#94712752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118473720-C-A

94712752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118473720-C-G

94712752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118473720-C-T

94712840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118473789-G-T

94712856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118473809-C-T

http://identifiers.org/hco/13/GRCh38#94712895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118473849-C-A

94712895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118473849-C-G

94712895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118473849-C-T

http://identifiers.org/hco/13/GRCh38#94712920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118473874-C-A

94712920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118473874-C-T

http://identifiers.org/hco/13/GRCh38#94712992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118473946-C-A

94713008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118473961-G-C

94713008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118473961-G-T

94713250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474206-A-G

http://identifiers.org/hco/13/GRCh38#94713333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118474297-C-A

94713344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474306-C-T

94713357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474319-C-T

94713358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474320-C-T

http://identifiers.org/hco/13/GRCh38#94713446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118474409-A-C

94713446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118474409-A-G

94713446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118474409-A-T

94713476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118474450-G-C

94713476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118474450-G-T

http://identifiers.org/hco/13/GRCh38#94713506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118474475-C-A

94713506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118474475-C-T

94713654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118474579-A-G

94713702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118474618-C-T

94713729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474646-G-A

94713729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474646-G-C

94713729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474646-G-T

94713744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118474662-T-C

94713816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118474725-G-A

94713816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118474725-G-T

94713965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474876-G-A

94713968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474879-G-A

94713978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474885-G-T

http://identifiers.org/hco/13/GRCh38#94714048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118474953-A-C

94714048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118474953-A-G

94714142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118475051-G-T

94714223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118475112-T-C

http://identifiers.org/hco/13/GRCh38#94714250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118475138-C-A

94714332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118475213-G-T

94714360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118475230-A-T

94714492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118475316-C-T

http://identifiers.org/hco/13/GRCh38#94714637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118475410-C-A

94714637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118475410-C-G

94714637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118475410-C-T

94715111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118475898-G-T

94715342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476116-A-T

94715496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476240-T-C

94715571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476315-A-G

94715580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476326-T-C

94715602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476356-C-G

94715602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476356-C-T

94715616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476371-T-A

94715816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476605-G-T

94715937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476729-G-T

94716227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476999-T-A

94716227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118476999-T-G

94716265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477039-G-A

94716265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477039-G-T

94716328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477107-C-T

94716485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477256-G-A

94716485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477256-G-T

94716514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477294-T-C

94716532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477312-G-A

94716550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477331-T-C

94716550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477331-T-G

94716652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477414-G-A

94717253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118477920-G-A

94721944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480341-T-C

94722014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480413-G-A

94722014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480413-G-T

94722049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480458-A-T

94722165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480571-T-G

94722169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480575-G-A

94722246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480614-C-T

94722290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480650-G-A

94722452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480876-C-T

94722472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118480894-C-G

94722822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118481256-G-C

http://identifiers.org/hco/13/GRCh38#94723194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118481585-C-A

94723194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118481585-C-T

94725839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118482959-A-G

94726231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118483967-A-G

94726400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484142-G-A

94726487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484222-T-A

94726512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484232-A-T

94726592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484312-G-T

94726695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484407-G-A

94726701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484412-A-T

94726720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118484431-A-G

94727836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485738-G-C

94727836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485738-G-T

94727970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485863-C-T

94728039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118485933-C-G

94728560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118486137-C-T

94728580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118486157-G-A

94728666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118486225-A-T

94738931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118491778-C-T

94739335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118492158-T-C

94739441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118492273-C-T

94739540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118492389-T-G

94739703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118492518-G-A

94743629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118493049-G-A

94743679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118493100-C-G

http://identifiers.org/hco/13/GRCh38#94743796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118493215-C-A

94743809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118493228-C-T

94743933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118493336-A-G

http://identifiers.org/hco/13/GRCh38#94744000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118493401-A-C

94744174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118493618-T-C

94747877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498457-T-G

94747918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498487-C-G

94748070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498640-T-A

94748070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498640-T-C

94748136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118498700-T-C

94749349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118499855-A-G

http://identifiers.org/hco/13/GRCh38#94749437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118499940-C-A

94749437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118499940-C-T

http://identifiers.org/hco/13/GRCh38#94749514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118500006-C-A

94749514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500006-C-G

94749592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500063-G-T

94750046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500259-A-G

94750235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500450-A-G

94750257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500471-C-T

94750540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500722-A-G

94750663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500847-T-C

94750668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500852-T-A

94750675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500859-C-G

94750746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500986-G-A

94750746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118500986-G-T

94750881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501121-T-C

94750927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501167-G-A

94750927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501167-G-C

http://identifiers.org/hco/13/GRCh38#94751282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118501514-C-A

94751459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501673-G-A

94751513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501725-C-T

94751687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501899-T-C

94751776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118501989-A-G

http://identifiers.org/hco/13/GRCh38#94751788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118502003-C-A

94751833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502045-T-C

94752170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502204-G-A

94752273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502312-T-G

94752317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502356-G-A

94752350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502393-T-C

94752568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502600-T-C

http://identifiers.org/hco/13/GRCh38#94752573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118502605-C-A

94752667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118502719-A-G

94753321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118503023-G-A

94753475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118503170-A-G

http://identifiers.org/hco/13/GRCh38#94753682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118503376-C-A

94753682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118503376-C-T

94761284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118508048-T-G

94761294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118508057-C-G

94761318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118508080-C-G

94761318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118508080-C-T

94761480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118508204-G-A

http://identifiers.org/hco/13/GRCh38#94761741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#118508499-C-A

94761745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118508503-A-G

http://identifiers.org/hco/13/GRCh38#94762118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118508694-C-A

94762118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118508694-C-T

94762357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118508780-A-G

94762441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118508867-T-C

94762501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118508923-T-C

http://identifiers.org/hco/13/GRCh38#94762533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118508952-A-C

94762544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118508963-G-A

94762608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118509122-C-G

94762770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118509281-T-C

94762846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118509352-A-G

94763356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118510267-T-A

94763356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118510267-T-G

94763392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118510303-T-C

94763430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118510340-T-C

94763810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118510654-A-T

94764080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511307-A-G

94764368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118511641-T-G

94770136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517686-G-A

94770198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517727-G-A

94770261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517794-A-G

94770336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517858-G-T

http://identifiers.org/hco/13/GRCh38#94770425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118517941-C-A

94770425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517941-C-T

94770445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517960-G-A

94770449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517964-A-G

94770463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118517984-G-T

94770567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518087-A-G

94770574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518102-T-C

94770614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518175-G-A

94770843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118518393-G-A

http://identifiers.org/hco/13/GRCh38#94770900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118518440-C-A

94771534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118520001-T-C

94771557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118520015-A-G

94772369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118520751-G-A

94772374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118520756-G-T

94772527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118520909-A-T

94772624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118521052-A-G

94772664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118521088-T-C

94772918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118521309-T-C

94773114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118521498-G-A

94773461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118522021-A-G

94775894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118524206-A-G

94776046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118524345-A-G

94776046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118524345-A-T

94776055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118524352-C-T

94776105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118524410-A-T

94776213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118524495-T-A

94776213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118524495-T-C

94776229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118524548-G-A

94776276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118524578-A-G

94776580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118524827-C-T

http://identifiers.org/hco/13/GRCh38#94776659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118524901-A-C

http://identifiers.org/hco/13/GRCh38#94776671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118524919-C-A

94776932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118525152-C-T

94778179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118526074-T-C

94778310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118526196-A-T

http://identifiers.org/hco/13/GRCh38#94778664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118526449-C-A

http://identifiers.org/hco/13/GRCh38#94778727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118526512-A-C

94780644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528477-C-G

94780697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118528505-T-C

94781548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118529157-G-C

94782828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118530414-C-G

94782996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118530555-T-C

94783180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118530731-C-T

http://identifiers.org/hco/13/GRCh38#94783195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118530748-C-A

94783206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118530818-T-C

http://identifiers.org/hco/13/GRCh38#94784247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118531562-C-A

http://identifiers.org/hco/13/GRCh38#94784523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118531851-C-A

94785214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118532458-T-C

94785216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118532460-G-T

94785630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118532890-C-T

94785675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118532930-A-G

94785675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118532930-A-T

94785749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533003-A-G

94785753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533007-T-G

94785845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533096-C-T

94786695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533884-C-T

94786720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533903-G-A

94786720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118533903-G-T

http://identifiers.org/hco/13/GRCh38#94786978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118534150-C-A

http://identifiers.org/hco/13/GRCh38#94787097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118534205-C-A

94787111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118534219-T-C

94787506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118534613-G-A

94787529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118534636-G-C

94787536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118534642-T-C

94787709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118534847-T-G

94787719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118534857-A-G

94787719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118534857-A-T

94787862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118535003-C-T

94788057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118535170-G-A

94788057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118535170-G-C

94788057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118535170-G-T

94788149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118535250-A-G

94788150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118535251-G-A

94794412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118539118-T-C

94794435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118539141-A-T

94794476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118539218-G-A

94794615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118539385-T-C

94794671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118539461-A-G

94794675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118539465-A-G

94794679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118539469-A-G

94794681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118539471-G-A

94795229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118540021-T-C

94795337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118540134-G-A

94795612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118540407-C-T

94797859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118541489-C-T

94797880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118541510-G-A

94797880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118541510-G-C

94797935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118541589-A-G

94797977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118541632-C-T

94798859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118542017-G-A

94798908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118542066-G-A

94798939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118542077-T-C

94799026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118542167-A-T

94799846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118543124-G-A

94799897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118543170-A-T

94799934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118543210-C-T

94800071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118543333-A-G

94800131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118543369-A-T

http://identifiers.org/hco/13/GRCh38#94800301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#118543534-A-C

94800312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118543544-C-G

94800395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118543631-G-A

94800413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118543649-T-C

94800775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118544002-C-T

94800785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118544011-C-T

94801007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118544228-C-G

94801483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118544332-C-T

94801491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118544340-C-T

94801706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118544482-C-T

94801727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118544503-T-A

94802462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39807
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118545031-A-G