62680304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859382-G-C

62680376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859456-A-G

62680388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89859468-C-T

http://identifiers.org/hco/13/GRCh38#62689667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89863200-C-A

62689667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863200-C-G

62689765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863299-A-G

62689795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863329-A-T

62689797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863331-C-G

62689797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863331-C-T

62689880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863399-C-T

62690108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863600-A-G

62690267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863755-G-T

62690327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863811-C-G

62690458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89863940-C-T

62692306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865230-T-C

http://identifiers.org/hco/13/GRCh38#62692355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89865268-C-A

62692409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865307-C-G

62692409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865307-C-T

62692464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865354-T-C

62692465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865355-C-T

62692497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865386-C-T

62692501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865390-T-C

62692501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865390-T-G

62692667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865551-A-G

62692722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865594-T-G

http://identifiers.org/hco/13/GRCh38#62693219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89865758-C-A

62693219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89865758-C-T

62693395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89866867-T-C

62693607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867048-T-C

62693607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867048-T-G

62693615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867056-C-G

62693622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867063-A-G

62693724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867157-A-T

62693731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867164-C-G

62693781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867234-T-C

62693830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867282-T-C

62693879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867328-A-G

62694093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867532-T-C

62694232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867666-C-G

62694232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867666-C-T

62694248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867682-C-G

62694248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867682-C-T

62694330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867762-C-G

http://identifiers.org/hco/13/GRCh38#62694364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89867796-C-A

62694364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867796-C-T

62694379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89867811-A-G

62697467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89869913-A-T

62697666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89870103-G-A

http://identifiers.org/hco/13/GRCh38#62697711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89870148-C-A

62697914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89870332-G-A

62698271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89870675-T-C

62698494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89870887-T-C

62698514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89870906-G-T

62698734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871037-T-A

62698843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871134-A-G

62698843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871134-A-T

62698933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871218-C-T

62699027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871303-T-A

62699028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871304-G-A

62699083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871346-T-C

62699141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871400-A-G

62699233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871482-T-A

62699234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871483-T-A

http://identifiers.org/hco/13/GRCh38#62699245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89871494-C-A

62699288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871539-A-T

62699319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871570-A-T

62699401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871626-T-G

62701658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89871901-C-G

http://identifiers.org/hco/13/GRCh38#62702333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89874002-A-C

62702333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874002-A-G

62702654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874264-G-A

62702654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874264-G-T

62702685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874296-C-G

62702685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874296-C-T

62702689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874300-C-T

62702759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874366-G-A

62702764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874371-C-T

62703018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874628-A-T

62703199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874794-C-T

62703243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874833-A-G

62703376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89874966-G-A

62703472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89875039-T-C

http://identifiers.org/hco/13/GRCh38#62703602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89875155-C-A

62703602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89875155-C-T

62703938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89875589-A-G

62704383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89876024-C-T

62704550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89876180-T-G

62704741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89876286-G-T

62704849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89876337-C-T

62704877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89876365-A-G

62705393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89878303-C-G

http://identifiers.org/hco/13/GRCh38#62705399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89878309-A-C

62707062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879124-T-C

62707077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89879139-C-T

62707273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880345-T-C

62707390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880445-G-A

62707397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880452-C-G

62707410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880465-T-A

62707410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880465-T-C

62707473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880528-T-C

62707690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880740-T-G

62707800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880815-T-C

62707917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880899-A-G

62707949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89880920-C-G

62708200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881137-A-G

62708200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881137-A-T

62708235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881166-C-T

62708258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881191-C-T

62708456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881368-G-C

62708463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881375-C-T

62708464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881376-A-G

62708482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881394-A-G

62708577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881450-C-T

62708619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881482-T-C

62708627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881490-G-A

62708650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881508-C-T

62708701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881559-C-T

62708711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881569-A-T

62708735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881597-T-A

62708764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881624-T-C

62708819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881688-A-T

62709005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881876-T-A

62709005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881876-T-C

62709024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881897-T-C

62709034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89881912-A-G

62709134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89882063-C-T

62709158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89882076-G-T

62709379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89882299-T-C

62709502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89882484-A-T

62709537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89882535-T-A

62709724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89882751-T-G

62709775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89882797-G-A

62709775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89882797-G-C

62709969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883000-T-A

62709990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883021-G-A

62710071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883096-G-A

http://identifiers.org/hco/13/GRCh38#62710098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89883124-A-C

62710098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883124-A-T

62710122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883148-C-T

62710161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883188-G-T

62710208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883230-T-G

62710429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883457-G-C

62710429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883457-G-T

62710487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883515-T-C

62710662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883695-C-G

62710672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883705-T-C

62710878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883906-T-C

62710884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883912-A-T

62710930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883952-G-A

62710953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89883974-T-C

http://identifiers.org/hco/13/GRCh38#62711064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89884082-C-A

62711064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884082-C-T

62711124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884142-T-C

62711405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884398-A-G

62711466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884458-T-A

62711466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884458-T-C

http://identifiers.org/hco/13/GRCh38#62711557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89884536-A-C

62711557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884536-A-T

62713279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89884965-G-A

62713587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89885252-T-C

62713611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89885295-C-T

62713669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89885342-G-A

62713678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89885351-A-G

http://identifiers.org/hco/13/GRCh38#62717230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89885510-A-C

62717897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887248-G-T

http://identifiers.org/hco/13/GRCh38#62718149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89887497-A-C

62718174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887522-T-C

62718219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887567-G-T

62718317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887682-C-T

62718414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887786-T-C

http://identifiers.org/hco/13/GRCh38#62718442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89887814-A-C

62718473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887845-C-T

62718479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89887851-T-C

62719774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888085-G-T

62720263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888486-A-G

62720265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888488-C-G

62720265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888488-C-T

62720299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888524-C-G

62720603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888832-T-C

62720631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888860-C-T

http://identifiers.org/hco/13/GRCh38#62720644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89888873-C-A

62720746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89888974-A-G

62721054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889306-C-G

62721261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889471-T-C

62721270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89889480-A-T

62744544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89891434-G-A

62744544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89891434-G-T

62748963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89896821-T-G

62749066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89896921-A-G

http://identifiers.org/hco/13/GRCh38#62749218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89897070-A-C

62749218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89897070-A-T

62749329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89897183-C-G

62749377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89897233-C-T

62749454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89897305-G-T

62749854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89897635-G-A

http://identifiers.org/hco/13/GRCh38#62749882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89897661-C-A

62749913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89897692-T-A

62749913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89897692-T-G

http://identifiers.org/hco/13/GRCh38#62749924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89897708-C-A

http://identifiers.org/hco/13/GRCh38#62749961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89897752-A-C

62753747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89901597-A-G

62754357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89903633-T-C

62754527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89903756-C-T

62754580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89903794-C-T

62754599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89903825-C-T

http://identifiers.org/hco/13/GRCh38#62754648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89903887-C-A

62754648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89903887-C-G

62754717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89903951-T-C

http://identifiers.org/hco/13/GRCh38#62754827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89904071-C-A

62754891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89904135-C-T

http://identifiers.org/hco/13/GRCh38#62754915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89904159-C-A

62754956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89904199-C-T

62754991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89904233-G-A

62765814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89911377-A-G

62765925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89911491-T-C

62766102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89911650-A-G

62766565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89912159-G-C

62766637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89912229-T-C

62777013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89932559-A-G

62780767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935087-G-A

62780994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935316-G-T

62781078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935378-A-G

62781168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935474-T-A

62781178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935484-A-T

62781316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935642-A-G

62781428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935752-C-T

62781492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935821-G-T

62781514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935845-T-A

62781592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935923-G-A

62781612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89935938-A-G

62781923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89936240-G-A

62781923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89936240-G-T

62784282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89936935-A-G

62784405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89937055-T-G

62784457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89937107-T-C

62784494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89937136-T-G

62784499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89937141-T-C

62794831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89940821-T-C

http://identifiers.org/hco/13/GRCh38#62794859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89940849-C-A

62794859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89940849-C-T

62794901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89940887-G-A

62794945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89940931-T-A

http://identifiers.org/hco/13/GRCh38#62794985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89940971-A-C

62795052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941049-G-A

62795101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941098-G-C

62795101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941098-G-T

62795146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941118-C-T

62795252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941218-G-C

62795291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941255-G-A

http://identifiers.org/hco/13/GRCh38#62795293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89941257-C-A

62795296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941260-T-A

62795296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941260-T-C

62795375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941342-A-T

62795445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941402-A-G

62795549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941503-A-G

62795588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941548-A-G

62795651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941827-T-A

62795651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941827-T-C

62795677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941928-T-C

http://identifiers.org/hco/13/GRCh38#62795688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89941939-C-A

http://identifiers.org/hco/13/GRCh38#62795695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89941946-A-C

http://identifiers.org/hco/13/GRCh38#62795704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89941955-C-A

62795722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89941973-C-G

62796121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89942324-T-C

62796129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89942332-C-T

62796147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89942349-T-C

62796208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89942402-T-C

http://identifiers.org/hco/13/GRCh38#62796268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#89942461-A-C

62796268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89942461-A-G

62796382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89942564-T-G

62796399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 89942578-G-A