25734664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84631504-G-A

25734664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84631504-G-T

http://identifiers.org/hco/21/GRCh38#25734673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84631513-C-A

25734673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84631513-C-G

25734673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84631513-C-T

25734744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84631584-A-G

http://identifiers.org/hco/21/GRCh38#25734965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#84631806-C-A

25734965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84631806-C-T

http://identifiers.org/hco/21/GRCh38#25735005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#84631846-C-A

25735005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84631846-C-G

25735005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84631846-C-T

http://identifiers.org/hco/21/GRCh38#25735129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#84631971-C-A

http://identifiers.org/hco/21/GRCh38#25735144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#84631982-C-A

25735144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84631982-C-T

25735185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84632019-G-A

25735185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84632019-G-C

25735185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84632019-G-T

25735237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84632071-T-A

25735251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84632085-A-G

25735286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84632146-G-A

25735286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 84632146-G-T

25735316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 84632168-T-A

25735316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 84632168-T-C

25735382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84632234-G-A

25735382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84632234-G-T

25735436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84632288-G-A

25735436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84632288-G-T

http://identifiers.org/hco/21/GRCh38#25735454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#84632306-C-A

http://identifiers.org/hco/21/GRCh38#25735485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#84632337-A-C

25735485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84632337-A-G

http://identifiers.org/hco/21/GRCh38#25735487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#84632339-C-A

25735487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 84632339-C-T

25735566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84632419-G-A

25735566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84632419-G-C

25735566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 84632419-G-T

25735645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84632497-T-G

25735745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84632586-G-A

25735745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84632586-G-T

25735817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84632646-G-A

25735817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84632646-G-T

25740918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84634929-C-T

25740986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84634985-C-T

25741477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84635872-G-T

25741480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84635875-G-A

25741480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84635875-G-T

http://identifiers.org/hco/21/GRCh38#25741581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84635977-C-A

25741581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84635977-C-T

25741682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84636078-G-A

25741682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84636078-G-C

http://identifiers.org/hco/21/GRCh38#25741733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84636126-C-A

25741733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84636126-C-G

25741734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84636127-A-G

25741800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84636182-G-A

25741808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84636193-T-G

25741817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84636202-C-G

25741817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84636202-C-T

25741818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84636203-T-C

25741823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84636208-T-C

25741891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84636277-A-G

25744594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84637355-T-C

http://identifiers.org/hco/21/GRCh38#25744622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84637382-C-A

25744622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84637382-C-G

25744626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84637386-T-C

25744779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84637524-T-C

25744863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84637762-C-T

25744917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84637815-C-T

25745054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84638056-A-G

25745054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84638056-A-T

http://identifiers.org/hco/21/GRCh38#25745068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84638064-A-C

25745143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84638163-G-A

25745149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84638169-T-A

25745166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84638174-G-A

25745166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84638174-G-C

25745166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84638174-G-T

25745309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84638316-A-G

25745459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84638396-A-T

25745837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84638770-C-T

25746408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84638993-G-A

25746683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84639289-G-A

25746842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84639467-G-A

25747466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84639808-G-T

http://identifiers.org/hco/21/GRCh38#25747601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84639933-A-C

25747601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84639933-A-G

http://identifiers.org/hco/21/GRCh38#25748396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84640474-A-C

25748396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84640474-A-T

25748413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84640490-A-G

25748601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84640650-C-T

25748648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84640697-T-C

25748895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84641043-T-C

http://identifiers.org/hco/21/GRCh38#25749134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84641268-C-A

25749134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84641268-C-T

http://identifiers.org/hco/21/GRCh38#25749248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84641375-C-A

25751978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84643002-C-T

25752053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84643076-T-A

25752134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84643157-C-T

25752191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84643214-G-A

25752267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84643286-A-G

25752289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84643305-T-A

25752289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84643305-T-C

25752311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84643330-T-C

25752429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84643448-A-G

25752470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84643491-G-A

25752470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84643491-G-T

25752475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84643496-G-A

25752643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84643664-G-T

25752673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84643701-G-T

25752814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84643863-G-A

25752848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84643925-A-G

25753094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84644122-G-A

25753148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84644252-G-A

25753211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84644313-T-C

25753329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84644407-T-C

25753383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84644459-G-C

http://identifiers.org/hco/21/GRCh38#25753583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84644768-A-C

25753623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84644802-C-T

25755934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84647182-G-C

25756373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84647657-C-T

25756385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84647669-C-T

25756393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84647677-T-A

25756522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84647966-C-G

25756525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84647969-T-C

25756525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84647969-T-G

25756598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84648038-C-T

25756877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84648379-C-G

25757257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84648594-G-T

25757401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84648744-G-A

25757844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649198-G-T

25757907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649258-G-T

http://identifiers.org/hco/21/GRCh38#25757916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84649261-C-A

25757916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649261-C-T

http://identifiers.org/hco/21/GRCh38#25757919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84649264-C-A

25757919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649264-C-G

25757919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649264-C-T

25757925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649270-G-A

25757925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649270-G-T

http://identifiers.org/hco/21/GRCh38#25757927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84649272-A-C

25757927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649272-A-G

25757927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649272-A-T

25757933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649278-G-A

25757933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649278-G-C

25757933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649278-G-T

25757948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649293-A-G

http://identifiers.org/hco/21/GRCh38#25758014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84649352-C-A

25758303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649638-T-A

http://identifiers.org/hco/21/GRCh38#25758312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84649649-A-C

25758312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649649-A-G

25758328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649667-A-G

25758419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84649794-G-A

25758546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84650022-C-T

25758608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84650079-G-A

25759180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84650501-G-A

25759303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84650623-G-A

25759342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84650662-A-G

25759522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84650732-G-A

25759856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84650932-G-A

25760164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84651201-C-T

25760256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84651289-A-G

25760385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84651381-A-G

25760608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84651616-G-A

25760864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84651807-C-T

25761211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84652545-G-C

25761370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84652689-A-G

25762195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84653239-G-A

25762195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84653239-G-T

25762218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84653262-T-A

25762218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84653262-T-C

25762334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: synonymous variant
orthologous variants: 84653372-A-G

25762401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84653442-T-A

http://identifiers.org/hco/21/GRCh38#25762451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84653486-A-C

25762451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84653486-A-G

http://identifiers.org/hco/21/GRCh38#25762868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84814640-C-A

25762893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84814625-A-G

25764160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84653874-T-C

25764433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654113-G-A

25764453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654133-G-A

http://identifiers.org/hco/21/GRCh38#25764454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84654134-C-A

25764454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654134-C-G

25764455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654135-A-G

25764474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654154-T-A

25764552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654229-C-G

25764569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654243-A-T

25764632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: synonymous variant
orthologous variants: 84654305-A-G

25764737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: synonymous variant
orthologous variants: 84654410-G-A

http://identifiers.org/hco/21/GRCh38#25764830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84654495-C-A

25764830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654495-C-G

25764830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654495-C-T

http://identifiers.org/hco/21/GRCh38#25764893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84654954-C-A

25764893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654954-C-G

25764894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654955-T-A

http://identifiers.org/hco/21/GRCh38#25764910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84654971-C-A

25764910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654971-C-T

25764934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654999-A-G

25764934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84654999-A-T

25765083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84655166-G-T

25768189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84656459-T-C

25768225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84656497-T-C

25768419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84656703-G-T

25768447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84656736-T-G

http://identifiers.org/hco/21/GRCh38#25768862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84657128-A-C

25768862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84657128-A-G

http://identifiers.org/hco/21/GRCh38#25768885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84657147-A-C

25768885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84657147-A-T

25768930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84657189-T-C

25768971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: intron variant
orthologous variants: 84657232-T-C

25769085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: synonymous variant
orthologous variants: 84657344-T-G

25769115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: synonymous variant
orthologous variants: 84657374-T-C

25769133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: synonymous variant
orthologous variants: 84657392-A-G

25769217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: synonymous variant
orthologous variants: 84657476-G-A

http://identifiers.org/hco/21/GRCh38#25769234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84657493-C-A

25769234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84657493-C-T

25769673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84657908-A-G

25769743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84657977-T-C

25769833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84658056-G-T

http://identifiers.org/hco/21/GRCh38#25770044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84658248-C-A

25770247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84658445-A-G

25770482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84658666-T-A

25770703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84658863-A-G

http://identifiers.org/hco/21/GRCh38#25770718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#84658877-C-A

25770718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84658877-C-T

25770836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84658931-G-A

25771434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84659459-G-T

25771494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84659499-A-T

25771553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84659563-G-T

25771840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84660034-G-A

25771954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4071
most severe consequence: 3 prime UTR variant
orthologous variants: 84660160-G-T