109560225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: non coding transcript exon variant
orthologous variants: 129763787-G-A

109560225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: non coding transcript exon variant
orthologous variants: 129763787-G-T

109560274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129763750-G-A

109560274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129763750-G-T

109560282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129763744-G-A

109560282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129763744-G-C

109560282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129763744-G-T

109560293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763733-A-G

http://identifiers.org/hco/4/GRCh38#109560298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#129763728-C-A

109560298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763728-C-T

109560306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763720-G-A

109560306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763720-G-T

109560312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763717-G-A

109560312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763717-G-C

109560312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763717-G-T

http://identifiers.org/hco/4/GRCh38#109560318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#129763711-C-A

109560318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763711-C-G

109560318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763711-C-T

http://identifiers.org/hco/4/GRCh38#109560344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129763689-C-A

109560344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 129763689-C-T

109560351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129763682-G-A

109560351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129763682-G-C

109560351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129763682-G-T

109560370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 129763663-G-A

109560370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 129763663-G-T

109560406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 129763627-G-A

109560406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 129763627-G-T

http://identifiers.org/hco/4/GRCh38#109560410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#129763623-C-A

109560410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763623-C-T

http://identifiers.org/hco/4/GRCh38#109560423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#129763610-C-A

109560423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763610-C-G

109560423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 129763610-C-T

109560458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129763585-T-C

109560494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129763549-G-A

109560494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129763549-G-C

109560494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129763549-G-T

109560495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129763548-G-A

109560495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129763548-G-C

109560495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129763548-G-T

109560933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129763231-C-G

109560971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129763214-G-A

109561004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129763183-T-C

109561122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129763069-A-G

109561140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129763052-G-T

109561240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129762989-C-T

109561292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129762950-G-T

109561407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129762791-G-C

http://identifiers.org/hco/4/GRCh38#109561420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#129762776-A-C

109561420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129762776-A-G

109561615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129762632-A-T

109561638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129762619-G-A

109562604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129762174-A-T

109562609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129762169-T-C

109562630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129762146-C-T

109562776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129761997-T-C

109562784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129761989-T-C

http://identifiers.org/hco/4/GRCh38#109563108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129761672-A-C

109563148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129761632-C-G

109563148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129761632-C-T

109563288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129761490-A-G

109563349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129761422-T-C

109563440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129761331-T-C

109563491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129761305-A-G

109563571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129761254-A-G

http://identifiers.org/hco/4/GRCh38#109563631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129761194-C-A

109563631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129761194-C-T

109567210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129756895-A-G

http://identifiers.org/hco/4/GRCh38#109567943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129756592-C-A

109567977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129756559-G-A

109567977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129756559-G-T

http://identifiers.org/hco/4/GRCh38#109567988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129756548-C-A

109567988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129756548-C-G

109567988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129756548-C-T

109568004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129756532-A-G

109568070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129756440-C-T

109568406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129756120-C-T

109568460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129756071-A-G

109568910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129755576-G-A

109568918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129755568-C-G

109568932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129755554-A-G

109569034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129755476-A-G

109569522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129755117-G-A

109569522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129755117-G-T

109570166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129752995-C-T

109570655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129752579-T-A

109570703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129752531-G-A

109570753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129752494-A-G

109570777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129752469-A-G

109571064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129752201-C-T

http://identifiers.org/hco/4/GRCh38#109571082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129752192-A-C

109571082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129752192-A-G

http://identifiers.org/hco/4/GRCh38#109571817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129750555-A-C

109571817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129750555-A-G

109571989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129750384-A-G

109572102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129750283-C-T

http://identifiers.org/hco/4/GRCh38#109572243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129750117-A-C

109572338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129750026-T-C

109572338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129750026-T-G

http://identifiers.org/hco/4/GRCh38#109572414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129749952-C-A

109572429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129749937-A-G

http://identifiers.org/hco/4/GRCh38#109574241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129749728-A-C

109574255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129749716-T-C

109574272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129749695-C-G

109574272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129749695-C-T

109574303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129749664-A-G

109574308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129749659-G-A

109574401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129749576-A-T

109574674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129749321-C-T

109574935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129749074-G-A

109575029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129748981-A-G

109575168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129748881-G-A

109575707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129748445-C-T

109575972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129747982-C-T

109576013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129747942-C-T

109576166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129747836-A-G

109576349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129747639-T-C

109576349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129747639-T-G

109577261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129746716-T-A

109577261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129746716-T-C

109577378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129746590-T-C

109577400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129746568-A-G

109577457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129746518-A-G

http://identifiers.org/hco/4/GRCh38#109577589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129746326-A-C

109577589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129746326-A-T

109610434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129744528-T-C

http://identifiers.org/hco/4/GRCh38#109611771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129743673-C-A

109611771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129743673-C-G

109615868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129738284-T-G

109615875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129738277-C-T

http://identifiers.org/hco/4/GRCh38#109616326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129737848-A-C

109616351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129737814-T-C

109616438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129737720-T-C

109616501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129737650-C-G

109619847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129735905-C-T

http://identifiers.org/hco/4/GRCh38#109619909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129735848-A-C

http://identifiers.org/hco/4/GRCh38#109619955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129735823-C-A

109620170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129735671-A-G

109620192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129735649-C-T

109620197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129735644-A-G

109620297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129735556-G-A

109620303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129735550-C-G

109620419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129735444-A-G

109620580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129735299-C-T

109620814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129735117-T-C

109620833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129735099-T-G

109621372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129734713-T-C

109621445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129734647-T-A

109621453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129734642-G-A

109621522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129734568-A-G

109621545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129734547-G-A

109621765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129734340-C-T

109621799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129734304-A-G

109626046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129733777-G-A

109633681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129732986-G-A

109633741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129732927-G-A

109633845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129732824-T-G

109634005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129732700-T-C

109636886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129731765-G-A

109636886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129731765-G-T

109641755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129731241-T-G

109641924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129731067-A-G

109642188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129730640-T-C

109642215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129730616-C-T

109642221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129730610-C-T

109642399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129730460-T-G

109658936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129728394-T-A

109658936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129728394-T-C

109658936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129728394-T-G

109658938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129728392-G-T

109658981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129728368-A-T

109659073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 129728285-G-A

109659073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 129728285-G-T

109659150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129728153-G-T

http://identifiers.org/hco/4/GRCh38#109659151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129728152-C-A

109659151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129728152-C-T

109659177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129728129-T-C

109660164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129727431-A-G

109660164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129727431-A-T

109660269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129727326-T-C

109660290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129727305-T-A

109660323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129727272-A-G

109660371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129727224-T-C

109660425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129727184-G-A

109660425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129727184-G-T

109660449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129727160-G-T

109660465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129727152-A-G

109660701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129727021-A-G

109660719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129727004-G-A

109660764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129726975-C-T

http://identifiers.org/hco/4/GRCh38#109660816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129726949-C-A

109660877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129726888-A-T

109660897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129726868-T-C

109661133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129726642-T-C

http://identifiers.org/hco/4/GRCh38#109661157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129726619-A-C

109661166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129726610-A-G

109661554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129726021-G-A

109662973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129724346-G-C

109663146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129724190-C-G

109663146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129724190-C-T

109663336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129724016-A-G

109663336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129724016-A-T

109663410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129723944-T-A

109663429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129723904-T-C

http://identifiers.org/hco/4/GRCh38#109663883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129722008-C-A

109664158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129720239-G-C

109664185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129720214-A-G

109664185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129720214-A-T

http://identifiers.org/hco/4/GRCh38#109664202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129720197-A-C

109664206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129720193-G-T

109664230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129720170-G-C

109664242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129720158-T-G

109664270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129720136-G-A

109664298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129720108-A-G

109664313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129720093-A-G

109664313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129720093-A-T

109664366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129720040-A-G

109664373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129720033-G-A

109664373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129720033-G-T

109664423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129719977-T-A

109664423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129719977-T-C

109673389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129717768-A-T

109673405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129717745-G-C

109673424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129717726-T-A

109673723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129717484-T-G

109682545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129712430-G-A

109682758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712217-G-A

109682758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712217-G-C

109682758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712217-G-T

109682763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712213-A-G

109682784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712192-T-A

109682784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712192-T-C

109682812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712157-G-A

109682812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712157-G-T

109682837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712136-G-A

109682837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712136-G-T

http://identifiers.org/hco/4/GRCh38#109682848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129712125-C-A

109682848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712125-C-G

109682848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712125-C-T

109682896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712068-C-T

http://identifiers.org/hco/4/GRCh38#109682915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129712050-C-A

109682922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712043-A-G

109682941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712024-A-G

109682945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712020-G-A

109682945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712020-G-T

109682946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712019-G-A

109682946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129712019-G-T

http://identifiers.org/hco/4/GRCh38#109682989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129711996-C-A

109682989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129711996-C-T

109683070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129711935-G-A

109683171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129711862-A-T

http://identifiers.org/hco/4/GRCh38#109683279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129711705-C-A

109683313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron variant
orthologous variants: 129711658-G-T

109683315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron variant
orthologous variants: 129711644-G-A

109683315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron variant
orthologous variants: 129711644-G-T

109683836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron variant
orthologous variants: 129711225-C-T

109683929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron variant
orthologous variants: 129711165-G-A

109684205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron variant
orthologous variants: 129711033-G-A

109684395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron variant
orthologous variants: 129710831-A-G

109684395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron variant
orthologous variants: 129710831-A-T

109684524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129710708-G-T

109684593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129710639-A-G

109684593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129710639-A-T

109684612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129710620-T-A

109684612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129710620-T-C

http://identifiers.org/hco/4/GRCh38#109684684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129710552-C-A

http://identifiers.org/hco/4/GRCh38#109684716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129709891-C-A

109684734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709874-T-G

109684777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709863-T-G

109684783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709857-T-C

http://identifiers.org/hco/4/GRCh38#109684813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129709826-C-A

http://identifiers.org/hco/4/GRCh38#109684821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129709818-A-C

109684822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709817-A-G

109685037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709632-T-A

109685162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709531-T-C

109685162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709531-T-G

109685164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709529-G-T

109685225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709489-T-C

109685225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709489-T-G

http://identifiers.org/hco/4/GRCh38#109685227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129709487-C-A

109685227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709487-C-G

109685227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709487-C-T

http://identifiers.org/hco/4/GRCh38#109685232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129709482-C-A

109685232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709482-C-G

109685232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129709482-C-T

109685270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129709447-T-C

109685316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129709401-A-T

109687394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129708950-T-A

109687433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129708911-G-A

109687439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129708905-A-T

109687452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129708892-A-G

http://identifiers.org/hco/4/GRCh38#109687487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129708858-C-A

109687487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129708858-C-T

109687522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129708826-A-G

109687541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129708807-T-C

109687555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129708793-T-C

109687568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129708780-A-G

109687593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129708755-T-C

109687597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129708751-A-G

109687649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129708702-G-T

109687730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708612-T-C

109687818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708541-G-A

109687818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708541-G-T

109687821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708538-G-A

109687821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708538-G-T

http://identifiers.org/hco/4/GRCh38#109687830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129708530-A-C

109687846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708514-G-A

109687846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708514-G-T

109687859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708501-T-G

http://identifiers.org/hco/4/GRCh38#109687860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#129708500-C-A

109687869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708490-G-T

109687880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708479-G-T

109687985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708345-C-T

109688188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708155-A-G

109688197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129708146-A-G

109688519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129707695-T-C

109688602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26076
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129707616-G-C