29527173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116846189-A-T

29527453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116845943-C-G

http://identifiers.org/hco/3/GRCh38#29527524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116845872-A-C

29527524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116845872-A-G

29527561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116845836-A-G

29527608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116845788-T-G

http://identifiers.org/hco/3/GRCh38#29527809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116845605-A-C

29527920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116845485-A-T

29528064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116845292-C-G

29528619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116844638-A-T

29529671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116843002-G-C

29531365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116840453-C-T

http://identifiers.org/hco/3/GRCh38#29531497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116840322-A-C

29532041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116839786-A-G

29532436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116839069-G-T

29532454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116839051-G-C

29532486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116839023-T-C

29532989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116838446-A-G

29532989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116838446-A-T

29533107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116838331-G-T

29534000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116837938-G-A

29534026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116837673-A-G

29534210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116837500-A-G

29534662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116837046-G-A

29534877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116836501-T-G

29535227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116836159-A-G

29535236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116836129-G-A

29535238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116836127-G-A

http://identifiers.org/hco/3/GRCh38#29536838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116833814-C-A

29536838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116833814-C-T

29538084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116831818-A-G

http://identifiers.org/hco/3/GRCh38#29538085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116831817-A-C

29538085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116831817-A-T

29538102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116831800-T-C

29538146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116831760-T-C

29538279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116831632-C-T

29538413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116831449-G-A

29538437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116831423-A-G

http://identifiers.org/hco/3/GRCh38#29538482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116831379-C-A

http://identifiers.org/hco/3/GRCh38#29538688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116831185-C-A

29538716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116831158-G-A

29538793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116831098-T-C

29539057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116829859-T-A

29539057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116829859-T-C

29539128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116829786-A-G

29548933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116828695-A-G

29549049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116828579-T-C

http://identifiers.org/hco/3/GRCh38#29549098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116828550-C-A

29549182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116828493-C-T

29549277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116828432-T-A

http://identifiers.org/hco/3/GRCh38#29549303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116828402-A-C

29549345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116828367-T-C

29549739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116828274-A-G

29549814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116828206-C-G

29549814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116828206-C-T

29549895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116828123-A-G

29552276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116820778-G-A

http://identifiers.org/hco/3/GRCh38#29552418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116820672-C-A

29552452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116820639-T-C

http://identifiers.org/hco/3/GRCh38#29552540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116820551-A-C

29552540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116820551-A-T

29552678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116820421-A-T

29552693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116820406-A-G

29552766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116820321-A-G

29557333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116810405-T-G

29557719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116809809-C-T

29557774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116809759-T-C

29558504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116808840-T-C

29558504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116808840-T-G

29558669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116808706-T-G

29558747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116808632-T-G

29559549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116807118-A-G

29559648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116807016-G-A

29559686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116806977-A-G

29559715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116806948-C-G

29559898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116806568-A-G

29559946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116806509-C-T

29560042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116806429-C-T

http://identifiers.org/hco/3/GRCh38#29560510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116805966-A-C

29563175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116804437-C-T

29563304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116804311-G-A

29563304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116804311-G-T

29563340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116804275-A-G

29563450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116804177-T-G

29563594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116804039-C-G

29563671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116803974-C-G

29563671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116803974-C-T

29564678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116803152-T-C

29565081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116802800-G-T

29567703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116799955-T-C

29567958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116799651-G-A

29568512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116799118-C-T

29568703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116798934-A-T

29568789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116798846-T-C

29568793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116798842-G-A

29568878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116798764-T-C

29569092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116798525-T-G

29569206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116798348-T-A

29569266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116798289-G-T

29569324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116798089-T-C

29569331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116798079-C-T

29579379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116796594-G-A

29579426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116796543-A-G

29579428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116796541-T-C

29579431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116796537-T-C

29579522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116796450-G-T

http://identifiers.org/hco/3/GRCh38#29579649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116796341-C-A

29579903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116796111-A-G

29580021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116796001-G-C

29580224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116795798-C-G

http://identifiers.org/hco/3/GRCh38#29580299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116795744-C-A

29580299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116795744-C-G

http://identifiers.org/hco/3/GRCh38#29582441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116795034-A-C

29582452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116795023-G-T

29582473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116794990-T-A

29582500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116794963-C-T

29582594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116794881-T-A

29582614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116794876-G-A

29582767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116794726-A-G

29584616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116792052-A-G

29584686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791991-T-C

http://identifiers.org/hco/3/GRCh38#29584696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116791982-C-A

29584701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791977-T-C

29584861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791833-G-A

29584861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791833-G-C

29584887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791808-A-G

29584922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791779-C-T

29584969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791740-A-G

29585145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791559-A-G

29585344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791372-T-G

29585372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791344-G-A

29585492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791236-T-C

29585559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791179-T-C

29585639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116791100-C-T

29585796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116790984-C-G

29586064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116790732-T-C

29586087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116790710-C-G

29586101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116790702-T-G

29586702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116789010-T-C

29586756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788953-A-G

29586843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788867-T-C

29586861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788849-T-C

29586900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788812-C-G

29586999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788721-G-A

29586999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788721-G-T

29587042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788680-T-C

29587210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788529-G-A

29587210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788529-G-T

29587211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788528-A-G

29587211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788528-A-T

29587212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 116788527-T-A

29587212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 116788527-T-C

29587212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 116788527-T-G

29587223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788515-G-A

29587223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788515-G-C

29587223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788515-G-T

29587224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788514-G-A

29587224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788514-G-C

29587224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788514-G-T

29587230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788508-T-A

29587230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788508-T-C

29587230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788508-T-G

29587236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788502-T-C

29587236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788502-T-G

29587237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788501-T-C

29587237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788501-T-G

29587275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788468-T-A

29587275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788468-T-C

29587275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788468-T-G

http://identifiers.org/hco/3/GRCh38#29587279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116788464-A-C

29587279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788464-A-G

29587279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788464-A-T

29587294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788449-G-C

29587294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788449-G-T

29587296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788447-T-A

29587296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788447-T-C

29587296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788447-T-G

29587303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788442-G-A

29587303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788442-G-T

29587321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788385-T-A

29587321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788385-T-C

29587321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788385-T-G

http://identifiers.org/hco/3/GRCh38#29587332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116788374-C-A

29587332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788374-C-T

29587408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788303-C-T

29587411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788300-C-T

29587473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788243-A-G

29587481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788228-A-G

29587562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788153-C-G

29587609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788065-G-T

29587619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116788046-C-G

29587694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116787973-T-C

http://identifiers.org/hco/3/GRCh38#29587753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116787920-A-C

29587922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116787756-A-G

29588267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116787298-A-G

29588269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116787296-C-T

http://identifiers.org/hco/3/GRCh38#29588541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116787023-C-A

29589072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116785722-A-G

29589230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116785528-C-T

29589287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116785471-A-G

29589403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116785357-A-G

29589680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116785060-G-A

29589724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116785016-G-A

29590237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116783938-T-G

29590260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116783915-T-C

29590271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116783904-A-G

29590285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116783884-G-T

29590681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116783092-A-G

http://identifiers.org/hco/3/GRCh38#29594580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116782064-C-A

29594657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116781983-G-T

29594867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116781754-G-A

29597563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116780806-C-T

29597686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116780688-G-C

29597814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116780586-C-T

29597832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116780568-T-A

29597832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116780568-T-C

29598122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116780075-G-A

29598361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116779860-A-G

29598374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116779847-T-G

29598445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116779777-A-G

29598445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116779777-A-T

29598449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116779771-A-G

29598706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116779171-T-C

http://identifiers.org/hco/3/GRCh38#29598717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116779160-C-A

29598717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116779160-C-T

29598809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116779072-G-A

29598815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116779066-C-T

http://identifiers.org/hco/3/GRCh38#29598876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116779001-C-A

29599077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116778791-A-G

29599079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116778789-T-G

29601781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116777770-G-A

29602007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116777590-T-A

29602317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116777295-T-C

29602401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116777212-T-C

http://identifiers.org/hco/3/GRCh38#29602414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116777199-A-C

29604643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116775496-A-G

http://identifiers.org/hco/3/GRCh38#29605073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116775105-C-A

29605239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774945-T-C

29605321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774865-G-A

29605321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774865-G-T

29605331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774855-A-T

29605344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774835-A-G

29605346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774833-G-A

29605492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774700-G-C

29605514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774680-G-C

29605558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774636-G-A

29605706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774491-C-T

29605844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774313-T-A

29605863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774294-G-A

29606015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774134-G-T

29606096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774051-A-G

29606108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116774039-T-C

http://identifiers.org/hco/3/GRCh38#29606124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116774023-C-A

29606183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116773973-C-G

29606194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116773962-A-G

29606231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116773927-C-T

29606845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116773040-A-G

29606927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116772965-C-T

29606955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116772946-G-A

29607008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116772903-T-C

29607008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116772903-T-G

29607112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116772800-G-A

29607113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116772799-T-A

29607124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116772788-T-C

29607130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116772780-A-G

http://identifiers.org/hco/3/GRCh38#29607400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116772591-C-A

29607400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116772591-C-G

http://identifiers.org/hco/3/GRCh38#29607523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116772483-C-A

29607594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116772413-T-C

http://identifiers.org/hco/3/GRCh38#29607775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116772225-A-C

http://identifiers.org/hco/3/GRCh38#29607799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116772184-C-A

29608289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116770697-C-T

29608318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116770679-T-C

http://identifiers.org/hco/3/GRCh38#29608330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116770667-A-C

29608401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116770612-G-A

29608517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116770522-G-A

29608724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116770357-G-T

29608762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116770320-C-T

29608827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116770270-A-G

29608835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116770262-G-A

29608857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116770239-T-C

http://identifiers.org/hco/3/GRCh38#29608951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116770149-C-A

29610036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116767818-T-G

29610065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116767786-C-G

29610065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116767786-C-T

29610271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116767608-A-G

29610459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116767301-A-G

29610481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116767286-C-T

29610482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116767285-C-T

29610523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116767259-C-G

29611702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116766923-G-A

29611784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116766242-A-G

29611784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116766242-A-T

29611925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116766095-T-C

29611970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116766063-C-T

29612035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116765991-T-G

29612817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116764492-A-T

29612839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116764470-T-C

29614675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116762904-G-T

29614680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116762899-A-G

29614778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116762813-A-T

29614906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116762695-T-G

29614989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116762627-A-T

29615177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116762470-G-T

http://identifiers.org/hco/3/GRCh38#29615582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116762103-A-C

29616630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759709-G-A

29616630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759709-G-T

29616659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759680-A-G

29616686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759650-G-A

29616686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759650-G-C

29616686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759650-G-T

29616791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759553-T-A

29616796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759548-G-A

29616796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759548-G-T

29616920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759424-T-C

29616924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116759420-T-C

29623213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116757304-C-G

29623214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116757303-T-G

29623233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116757284-T-C

29623238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116757279-T-A

29623265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116757254-C-T

29623266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116757253-G-A

29623712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116757114-G-A

29624021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116756837-A-G

29624734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116755588-A-G

29625788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116755273-T-G

29625789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116755272-T-C

29626006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116755060-G-A

29626006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116755060-G-C

29626141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116754600-T-C

29626142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116754599-G-A

29626232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116754522-G-C

29626232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116754522-G-T

29626265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116754455-G-A

29628822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116753530-A-G

http://identifiers.org/hco/3/GRCh38#29628838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116753514-A-C

29628838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116753514-A-G

29628910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116753450-A-G

29628974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116753397-T-A

29629021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116753371-C-T

http://identifiers.org/hco/3/GRCh38#29629106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116753313-C-A

29629249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116753177-G-A

29629249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116753177-G-C

29629298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116753121-T-C

29629392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116753028-A-G

29629721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116752712-T-A

29629740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116752691-C-G

29631525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116749188-A-G

29631624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116749087-A-G

http://identifiers.org/hco/3/GRCh38#29631634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116749077-C-A

29631634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116749077-C-T

http://identifiers.org/hco/3/GRCh38#29631658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116749054-A-C

29631658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116749054-A-G

http://identifiers.org/hco/3/GRCh38#29631734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116748980-A-C

29631855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116748859-T-G

29631938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116748776-C-G

29631938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116748776-C-T

29631952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116748763-A-G

29632163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116748548-G-T

29632190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116748521-T-C

29632264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116748473-G-A

29632265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116748472-A-G

29632281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116748456-A-G

29632325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116748415-A-G

29632666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116747529-G-C

http://identifiers.org/hco/3/GRCh38#29632868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116747313-C-A

29632881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116747301-C-T

29633343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116746295-A-G

29633453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116746186-T-G

http://identifiers.org/hco/3/GRCh38#29633514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116746148-C-A

29633514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116746148-C-T

29633715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116745949-C-G

29633749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116745903-T-C

29633792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116745863-A-T

http://identifiers.org/hco/3/GRCh38#29633900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116745779-C-A

29633937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116745745-A-G

29633947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116745735-A-G

29634049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116745254-A-G

29634191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116745144-G-A

29634266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116745068-T-C

29634284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116745050-G-A

29634429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116744925-A-T

29634439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116744909-G-T

29634442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116744906-G-A

29634632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116744740-A-G

http://identifiers.org/hco/3/GRCh38#29634724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116744693-C-A

29634746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116744670-A-G

29635931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116742780-C-G

29635931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116742780-C-T

29636142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116742547-C-T

29636278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116742406-C-T

29636396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116742287-A-G

29636396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116742287-A-T

29636479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116742217-T-C

29636493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116742203-G-A

29636776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116741922-A-G

29636841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116741857-G-A

29637009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116741696-A-T

29637142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116741629-T-A

29637581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116741067-C-T

29637755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116740018-A-G

http://identifiers.org/hco/3/GRCh38#29637951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116739825-A-C

29637983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116739802-G-T

29638506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116738853-A-T

29638803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116738562-T-A

29638828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116738537-T-A

29638829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116738536-A-G

29639141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116738272-C-T

http://identifiers.org/hco/3/GRCh38#29639257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116738159-A-C

29639257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116738159-A-G

http://identifiers.org/hco/3/GRCh38#29639431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116737991-C-A

http://identifiers.org/hco/3/GRCh38#29639550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116737879-C-A

29641729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116737400-G-A

29641779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116737356-A-G

29641796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116737340-A-T

29641995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116737188-C-G

29642039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116737145-G-T

29642178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 116737004-G-A

http://identifiers.org/hco/3/GRCh38#29642736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116735444-A-C

29642756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116735424-C-T

http://identifiers.org/hco/3/GRCh38#29642778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#116735408-C-A

29642778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39988
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 116735408-C-T