http://identifiers.org/hco/1/GRCh38#66925181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#102971798-C-A

66925181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: 102971798-C-G

66925181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: 102971798-C-T

66925200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: 102971819-G-A

66925200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: 102971819-G-T

66925223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: 102971842-T-C

66925223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: 102971842-T-G

66925258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: 102971875-T-A

66925258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: 102971875-T-C

66925258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: 102971875-T-G

66925297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, undefined
orthologous variants: 102971923-C-T

66925496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102972152-C-T

66925779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 102972417-C-T

66925911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102972535-T-A

66926332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 102972940-A-G

66926469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102973088-T-C

66926874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102973415-A-G

66926924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102973461-T-C

66926931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102973468-A-G

66926931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102973468-A-T

66927007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102973544-A-G

66927128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102973722-A-G

66927340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974006-A-G

66927487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974161-T-C

66927487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974161-T-G

66927575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974241-A-G

66927622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974288-A-G

66927721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974388-T-C

66927748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102974419-A-G

66927766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974437-G-A

66927766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974437-G-T

66927786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974462-G-A

66928128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974759-A-G

66928162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102974786-C-T

66928442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102975037-T-C

66928541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102975139-T-A

66928541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102975139-T-C

66929226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102975777-G-A

66929226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102975777-G-T

66929318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102975849-C-T

66929916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102976336-T-A

http://identifiers.org/hco/1/GRCh38#66930154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102976488-C-A

66930154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102976488-C-T

66930163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102976496-G-A

66930163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102976496-G-T

66930184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102976517-A-G

66930184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102976517-A-T

http://identifiers.org/hco/1/GRCh38#66930236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#102976567-C-A

66930236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102976567-C-G

66930236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102976567-C-T

66930281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102976600-G-C

66930360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102976666-C-T

66930429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102976730-C-T

http://identifiers.org/hco/1/GRCh38#66930491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#102976778-C-A

66930491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102976778-C-G

66930491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102976778-C-T

66930552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102976832-G-A

66930552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102976832-G-T

66930764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102977002-T-C

66930764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102977002-T-G

66930803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102977064-A-G

66931100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102977305-T-C

66931100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102977305-T-G

66931504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102977750-G-A

66931999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102978413-G-C

66932220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102978557-A-G

66932287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102978627-T-C

66932662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102978980-A-G

66932789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102979064-G-A

66932789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102979064-G-T

66933008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102979271-G-A

66933089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102979348-G-A

66933655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102979904-A-G

66933731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102979977-A-G

http://identifiers.org/hco/1/GRCh38#66934072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102980170-A-C

66934243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102980341-C-T

66934868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102980594-G-A

66934937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102980655-G-C

66935105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102980776-C-G

66935107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102980778-A-G

http://identifiers.org/hco/1/GRCh38#66935592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102981213-A-C

66937628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102982050-T-A

66938378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102982901-A-G

66938550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102983127-G-T

66938768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102983313-G-A

66938794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102983338-A-G

66938887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102983444-T-C

66939300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102983808-A-G

66939338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102983846-G-T

http://identifiers.org/hco/1/GRCh38#66939941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102984392-C-A

66939941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102984392-C-T

http://identifiers.org/hco/1/GRCh38#66940094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102984538-C-A

66940094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102984538-C-T

66940155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102984580-T-C

66940265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102984594-G-C

66940265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102984594-G-T

http://identifiers.org/hco/1/GRCh38#66940384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102984699-C-A

66940384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102984699-C-T

66940549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102984826-G-A

http://identifiers.org/hco/1/GRCh38#66941152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102985115-C-A

66941389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102985319-A-T

66942239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102985594-G-A

66942239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102985594-G-T

66942337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102985687-G-A

http://identifiers.org/hco/1/GRCh38#66942515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102985843-A-C

66942613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102985917-G-A

66942646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102985954-A-G

66942668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102985976-C-G

66943096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102986538-G-A

66943817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102986951-T-C

66943866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102987000-C-T

66944017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102987133-A-T

66944084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102987192-A-G

66944168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102987265-C-T

66944717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 102987674-T-G

66946302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 102988315-A-G

66946328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988338-G-A

66946328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988338-G-T

66946391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988393-G-A

66946391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988393-G-T

66946506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988478-A-G

66946556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988505-G-A

66946556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988505-G-T

http://identifiers.org/hco/1/GRCh38#66946564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102988513-A-C

http://identifiers.org/hco/1/GRCh38#66946622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102988571-A-C

66946622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988571-A-G

66946894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988815-T-G

66947028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988971-C-G

66947056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102988999-C-T

66947088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102989013-G-C

66947163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 102989073-G-T

66947416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989470-C-G

http://identifiers.org/hco/1/GRCh38#66947524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102989581-C-A

http://identifiers.org/hco/1/GRCh38#66947619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102989674-C-A

66947619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989674-C-T

66947656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989708-T-C

66947658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989710-C-T

66947802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989839-A-G

66947807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989844-A-G

66947807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989844-A-T

http://identifiers.org/hco/1/GRCh38#66947811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102989848-C-A

66947811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989848-C-G

66947811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989848-C-T

66947852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989893-A-G

66947852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989893-A-T

http://identifiers.org/hco/1/GRCh38#66947879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102989912-C-A

66947968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989974-G-A

66947978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102989984-T-C

66948179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102990087-A-G

http://identifiers.org/hco/1/GRCh38#66948211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102990094-C-A

66948219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102990102-T-C

66948260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102990140-T-C

66948277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102990157-G-A

66948352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102990201-G-A

66948352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102990201-G-T

66949553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102990582-G-A

http://identifiers.org/hco/1/GRCh38#66949805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102990835-A-C

66949805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102990835-A-T

66949871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102990960-T-C

66949886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102990979-C-T

http://identifiers.org/hco/1/GRCh38#66951782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102991666-C-A

66951826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102991714-G-A

66951826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102991714-G-T

66951945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102991811-C-T

66952025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102991880-T-C

66952117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102991963-C-T

66952122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102991968-A-G

66952179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102992022-A-G

66952300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102992134-C-G

66955640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102994144-A-G

http://identifiers.org/hco/1/GRCh38#66955713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102994212-A-C

66955872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102994358-G-A

66955872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102994358-G-T

66957062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102995618-G-A

66957062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102995618-G-C

http://identifiers.org/hco/1/GRCh38#66957140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102995694-C-A

66957267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102995814-C-T

66957277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102995824-G-A

66957549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102996096-C-T

66957763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102996286-T-A

66957956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102996439-T-A

66958024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102996521-G-A

66958024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102996521-G-T

66958032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102996530-G-T

66958044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 102996540-T-G

66958154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102996647-A-G

66958289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102996786-T-G

http://identifiers.org/hco/1/GRCh38#66958351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102996846-C-A

66958351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102996846-C-T

66958449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102996936-T-C

66958683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102997160-T-C

66958731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102997207-T-C

http://identifiers.org/hco/1/GRCh38#66958813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102997275-C-A

66958813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102997275-C-T

66958839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102997296-A-T

66959616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102997971-T-C

66959616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 102997971-T-G

http://identifiers.org/hco/1/GRCh38#66959764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102998107-C-A

66959764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102998107-C-T

http://identifiers.org/hco/1/GRCh38#66959925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102998255-A-C

http://identifiers.org/hco/1/GRCh38#66960078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102998323-A-C

66960078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102998323-A-G

http://identifiers.org/hco/1/GRCh38#66960158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102998402-C-A

66960158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102998402-C-G

66960158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102998402-C-T

66960356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102998506-G-A

66960356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102998506-G-T

66960515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102998667-A-G

66961889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102999292-G-T

66961932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102999335-G-A

66961946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102999347-A-G

66962003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102999407-C-G

66962010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102999414-C-G

66962070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 102999477-T-C

66962946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103000211-G-A

http://identifiers.org/hco/1/GRCh38#66962948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103000213-A-C

66963022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103000276-G-A

66963022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103000276-G-T

http://identifiers.org/hco/1/GRCh38#66963041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103000294-A-C

http://identifiers.org/hco/1/GRCh38#66963249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103000763-C-A

66963249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103000763-C-T

66963536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103000991-C-T

66963539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103000994-A-G

66964996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: -C-G

66965095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: -T-C

66965103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: -T-C

66965166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: -G-C

66965257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: -T-G

66965331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: -A-G

http://identifiers.org/hco/1/GRCh38#66969577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103004344-C-A

66969577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103004344-C-T

66969753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103004504-A-G

66970784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103005473-T-C

66970821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: synonymous variant
orthologous variants: 103005509-T-C

66970845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: missense variant
orthologous variants: 103005533-G-T

66970851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: synonymous variant
orthologous variants: 103005539-A-G

66970851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: missense variant
orthologous variants: 103005539-A-T

66970887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: synonymous variant
orthologous variants: 103005575-A-G

66970905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: missense variant
orthologous variants: 103005593-T-G

66970941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: synonymous variant
orthologous variants: 103005629-C-T

66970944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: missense variant
orthologous variants: 103005632-A-G

66971313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103005969-T-G

66971458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103006131-A-G

66971573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103006230-G-A

66971573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103006230-G-T

66971580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103006237-G-A

66971580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103006237-G-T

66971618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103006283-A-G

66971618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103006283-A-T

66971638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103006303-G-A

http://identifiers.org/hco/1/GRCh38#66971639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103006305-C-A

66971762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103006429-A-G

66971890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103006551-C-T

66972195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103007019-C-G

66972252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103007043-A-G

66972261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103007052-T-C

66972261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103007052-T-G

66972333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103007125-A-G

66972393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103007180-C-G

66972408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103007194-A-G

66972735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103007579-A-G

http://identifiers.org/hco/1/GRCh38#66972775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103007619-A-C

66972802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103007646-A-G

66972815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103007665-G-T

66973003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103007840-T-C

66974835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103009533-T-C

66974867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103009567-G-A

66974972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103009658-A-T

66976449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103012015-A-G

66976519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103012608-T-C

66976783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103012843-T-A

66976783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103012843-T-C

66977291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103013245-T-C

66978260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103013731-G-A

66978376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103013829-G-T

66978466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103014009-T-A

66978542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103014060-G-C

66978749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103014302-A-G

66978749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103014302-A-T

66978886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103014446-T-C

66979107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103014678-T-A

66979108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103014679-A-G

66979108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103014679-A-T

66979415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103015437-T-A

66981463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103016574-A-G

66981512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103016622-C-T

66981634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103016731-G-T

66981761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103016857-T-G

66981791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103016891-T-C

66981917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 103017017-T-C

66981926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 103017026-A-T

http://identifiers.org/hco/1/GRCh38#66982623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103017680-A-C

66982756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103017786-G-A

http://identifiers.org/hco/1/GRCh38#66982800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103017836-C-A

http://identifiers.org/hco/1/GRCh38#66982947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103018044-C-A

66982947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103018044-C-G

66982950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: intron variant
orthologous variants: 103018047-A-G

66984923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103019971-T-G

http://identifiers.org/hco/1/GRCh38#66985404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103020377-A-C

66985751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103020723-T-C

66985751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103020723-T-G

66985897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103020860-T-C

66985897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103020860-T-G

http://identifiers.org/hco/1/GRCh38#66985969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103020932-A-C

66986063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021032-G-T

66986127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021100-T-C

66986127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021100-T-G

66986346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021315-A-G

66986457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 103021429-A-G

http://identifiers.org/hco/1/GRCh38#66986548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103021513-A-C

66986548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021513-A-G

http://identifiers.org/hco/1/GRCh38#66986632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103021570-A-C

http://identifiers.org/hco/1/GRCh38#66986647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103021585-C-A

66986647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021585-C-T

http://identifiers.org/hco/1/GRCh38#66986660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103021596-C-A

http://identifiers.org/hco/1/GRCh38#66986671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103021604-C-A

66986671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021604-C-G

66986671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021604-C-T

66986686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021619-C-G

66986686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021619-C-T

66986704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103021637-C-G

66987267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103022369-A-T

66987443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103022719-T-A

66987480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103022767-G-A

66987489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103022776-T-C

66987495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29657
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103022782-A-G