http://identifiers.org/hco/3/GRCh38#111674703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45830751-A-C

111674703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45830751-A-G

111674703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45830751-A-T

111674841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5 prime UTR variant
orthologous variants: 45830620-G-A

111674841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5 prime UTR variant
orthologous variants: 45830620-G-C

111674841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5 prime UTR variant
orthologous variants: 45830620-G-T

111674901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5 prime UTR variant
orthologous variants: 45830561-T-C

111674901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5 prime UTR variant
orthologous variants: 45830561-T-G

111674936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5 prime UTR variant
orthologous variants: 45830526-A-G

111675061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5 prime UTR variant
orthologous variants: 45830401-G-T

111675076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5 prime UTR variant
orthologous variants: 45830386-G-T

111675092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5 prime UTR variant
orthologous variants: 45830371-G-T

111675394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: missense variant
orthologous variants: 45830069-A-G

111675442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45830021-T-C

http://identifiers.org/hco/3/GRCh38#111675534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45829931-C-A

111675705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45829743-T-C

111676275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45829179-G-A

111676337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45829123-A-G

111676609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45828846-G-T

http://identifiers.org/hco/3/GRCh38#111676678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45828777-C-A

111676704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45828754-G-A

http://identifiers.org/hco/3/GRCh38#111676760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45828696-C-A

111677010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45828466-G-A

111677032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45828450-C-T

111677243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45828243-A-G

111677304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45828182-T-C

111677378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45828109-G-A

111677504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45827831-G-T

http://identifiers.org/hco/3/GRCh38#111677579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45827751-C-A

http://identifiers.org/hco/3/GRCh38#111677876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45827089-C-A

111678107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45826836-T-G

111678146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45826797-T-A

111678192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45826740-C-T

111678258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45826673-A-G

http://identifiers.org/hco/3/GRCh38#111678282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45826647-C-A

111678282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45826647-C-T

111678354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45826575-T-C

111678357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45826572-A-G

111679252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45826111-G-A

111679296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45826070-G-A

111679296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45826070-G-C

111679380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45825994-T-C

http://identifiers.org/hco/3/GRCh38#111679439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45825953-C-A

http://identifiers.org/hco/3/GRCh38#111679557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45825829-A-C

111680035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45825241-T-C

111680057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45825223-G-A

111680165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45825091-C-T

111680428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45824445-A-G

111680930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45823614-A-G

111681996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45822389-G-T

111682020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45822365-A-G

111682037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45822348-G-C

111682325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45822068-A-G

111682542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45821800-C-T

111682862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45821405-G-T

111683544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45820380-G-C

111683651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45820260-C-T

111684877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45819586-T-C

http://identifiers.org/hco/3/GRCh38#111684932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45819511-A-C

http://identifiers.org/hco/3/GRCh38#111684945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45819498-A-C

111684997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45819451-A-G

111685458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45818758-C-T

111685506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45818709-C-T

111685556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45818659-T-G

111685932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45818337-G-T

http://identifiers.org/hco/3/GRCh38#111686054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45818207-C-A

111686235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45818043-G-T

111686681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45817598-A-T

111686926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45817370-G-A

111687057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45817230-G-A

111689261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45814013-A-T

111689526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45813742-C-T

111689648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45813626-T-C

111689649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45813625-A-G

111689677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45813597-C-T

111690279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45813028-T-C

111690292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45813015-G-A

111690643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45812711-C-T

111691317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45811923-G-C

111691317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45811923-G-T

111691513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811754-G-A

111691552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811692-T-C

111691961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811393-G-T

111692377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811112-G-T

111692430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45811088-A-T

111692482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45811039-G-T

111693022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810560-G-A

111693323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810305-C-T

111693431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810227-G-A

111693647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810015-C-T

111693649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45810012-C-T

111693864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809804-G-A

111693907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809768-A-G

111693941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45809734-C-T

111696371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808864-A-T

111696526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808707-T-G

111698037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808600-A-G

111698357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808334-C-G

111698409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45808283-T-A

111698993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807442-G-A

111699040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807399-G-A

http://identifiers.org/hco/3/GRCh38#111699207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45807237-C-A

111699383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45807063-C-T

111699623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806754-A-G

111699784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806594-G-T

http://identifiers.org/hco/3/GRCh38#111700461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45806151-A-C

111700461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45806151-A-G

111703991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804700-T-G

111704395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45804101-C-G

111707518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801443-T-C

http://identifiers.org/hco/3/GRCh38#111707786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45801160-C-A

111707842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45801112-G-T

http://identifiers.org/hco/3/GRCh38#111708297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45800686-C-A

111708297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: missense variant
orthologous variants: 45800686-C-T

http://identifiers.org/hco/3/GRCh38#111708432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45800552-C-A

http://identifiers.org/hco/3/GRCh38#111708514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45800474-A-C

111708514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45800474-A-G

111708535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45800453-T-C

111710570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45797128-C-T

111710584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45797115-C-G

111710641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45797088-G-T

111710660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45797069-G-T

111711532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45796107-A-T

111711538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45796101-G-A

111711546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45796090-G-A

111711570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45796066-G-C

111711584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45796052-A-G

111712234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45795006-G-A

111712234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45795006-G-T

111712348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45794890-G-A

http://identifiers.org/hco/3/GRCh38#111712655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45794598-C-A

111712655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45794598-C-T

111712678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45794577-G-C

111712744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45794524-G-A

111713209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45794071-C-T

111713282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45793995-A-G

111713394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45793878-C-T

111713673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45793616-C-T

111714138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45792460-T-C

111714147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45792451-C-T

111714150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45792448-A-G

http://identifiers.org/hco/3/GRCh38#111714249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45791667-C-A

111714254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45791662-A-G

111714259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45791657-T-C

111714382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45791539-C-T

111714397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45791521-C-T

111714433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45791479-G-A

http://identifiers.org/hco/3/GRCh38#111714652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45791286-C-A

111714778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45791154-G-A

111714784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45791148-A-G

111715015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45790700-T-A

111715015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45790700-T-G

111715170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45790508-T-G

111715209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45790347-T-C

111715237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45790188-C-T

http://identifiers.org/hco/3/GRCh38#111715410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45790003-A-C

111715423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45789990-T-G

http://identifiers.org/hco/3/GRCh38#111715517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45789908-A-C

111715824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45789613-T-G

111715958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45789489-A-T

111715999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45789449-G-T

111716021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45789439-C-T

111716022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45789438-G-A

http://identifiers.org/hco/3/GRCh38#111716098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45789391-A-C

http://identifiers.org/hco/3/GRCh38#111716131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45789359-C-A

111716131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45789359-C-T

111716207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45789284-T-C

http://identifiers.org/hco/3/GRCh38#111716228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45789261-A-C

http://identifiers.org/hco/3/GRCh38#111716351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45789119-C-A

111716756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45788675-A-T

111716764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45788667-G-A

111717014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45788301-G-T

111717140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45788179-T-G

111717702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45788069-T-C

111717799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45787976-A-G

111717971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45787815-T-C

111718783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45787320-G-T

111719137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45787007-A-G

111720658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45785603-T-C

111720662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45785599-G-A

111720871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, missense_variant
orthologous variants: 45785390-G-T

111721129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45785129-G-T

http://identifiers.org/hco/3/GRCh38#111721309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45784958-C-A

111721309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784958-C-T

111721365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784902-A-G

111721640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784645-C-T

111721746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784539-G-A

111721746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784539-G-T

111721775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784512-A-G

111721794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784493-G-A

http://identifiers.org/hco/3/GRCh38#111721873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45784431-C-A

111721879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784425-A-G

111721880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784421-G-A

111721880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784421-G-T

111721962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784339-G-A

111722223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45784073-A-T

http://identifiers.org/hco/3/GRCh38#111722384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45783914-C-A

111722426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45783872-A-G

111722519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45783788-T-A

111722555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45783751-G-A

111722559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45783747-T-C

111722666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45783642-G-A

http://identifiers.org/hco/3/GRCh38#111722706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45783605-C-A

111722706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45783605-C-T

111722753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45783561-C-T

http://identifiers.org/hco/3/GRCh38#111722856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45783461-A-C

111723051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45783257-C-T

111723120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45783178-T-G

111723206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45783093-A-G

http://identifiers.org/hco/3/GRCh38#111723369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45782936-C-A

111723400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782910-G-T

111723428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782882-C-T

111723431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782879-G-A

111723569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782737-A-G

111723657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782673-A-G

111723674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782659-A-G

111723715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782619-A-G

111723759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782577-T-G

http://identifiers.org/hco/3/GRCh38#111723825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45782508-C-A

http://identifiers.org/hco/3/GRCh38#111724044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45782314-C-A

111724044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782314-C-T

111724141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782210-G-A

111724147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782204-G-A

111724147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782204-G-T

111724148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45782203-A-G

111724665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781654-G-T

111724805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781565-G-T

111724969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781433-A-G

111724980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781422-C-T

111724993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781409-C-T

111724995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781407-G-T

111725002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781399-T-C

111725009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781392-C-T

111725018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781382-G-T

http://identifiers.org/hco/3/GRCh38#111725054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45781349-C-A

111725054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781349-C-T

111725077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781326-C-T

111725092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781311-C-T

111725102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781301-G-A

111725103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781300-A-T

http://identifiers.org/hco/3/GRCh38#111725106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45781297-C-A

111725106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781297-C-T

111725149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781259-T-A

111725150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781258-A-G

111725169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781239-G-T

111725172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781236-C-T

111725237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781199-A-G

http://identifiers.org/hco/3/GRCh38#111725247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45781189-C-A

111725266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781170-G-T

111725274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781162-T-C

http://identifiers.org/hco/3/GRCh38#111725331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45781101-C-A

111725354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781079-G-A

111725354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781079-G-T

111725368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781065-T-C

111725386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781047-T-A

111725407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45781024-G-C

111725544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780884-G-A

http://identifiers.org/hco/3/GRCh38#111725545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45780883-C-A

http://identifiers.org/hco/3/GRCh38#111725571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45780859-C-A

111725571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780859-C-T

111725634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780809-C-T

111725669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780785-G-A

111725757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780713-C-T

111725763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780707-A-T

111725772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780698-G-A

111725775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780695-T-C

111725783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780687-C-T

111725787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780684-A-G

http://identifiers.org/hco/3/GRCh38#111725807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45780664-C-A

111725810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780661-C-T

111725825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780646-T-A

111725825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780646-T-C

111725830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780642-T-C

111725874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780598-T-A

111725898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780575-T-A

111725904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780569-G-T

111725910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780563-T-A

111725910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780563-T-C

http://identifiers.org/hco/3/GRCh38#111725971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45780539-A-C

111725971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780539-A-G

111726007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780503-T-C

http://identifiers.org/hco/3/GRCh38#111726043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45780468-C-A

111726176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780331-T-A

111726176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780331-T-C

111726203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780304-T-C

111726206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780301-G-T

111726229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780278-A-T

111726245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780262-T-C

111726352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45780170-G-A

http://identifiers.org/hco/3/GRCh38#111726400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45780119-C-A

http://identifiers.org/hco/3/GRCh38#111726432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45780088-C-A

111726530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45779990-A-G

111726777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45779748-A-G

111726892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45779620-G-A

111727024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45779508-T-C

111727076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45779495-T-C

http://identifiers.org/hco/3/GRCh38#111727136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45779434-C-A

111727272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45779313-A-T

111727379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45779204-G-A

111727485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45779099-G-A

111727485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45779099-G-C

111727633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45778970-C-G

111727657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45778950-T-C

111727944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45778676-A-G

http://identifiers.org/hco/3/GRCh38#111727958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45778662-C-A

111727958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45778662-C-G

http://identifiers.org/hco/3/GRCh38#111727971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45778646-A-C

111728277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45778446-G-A

111729075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45777582-T-A

http://identifiers.org/hco/3/GRCh38#111729121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45777529-A-C

111729224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45777420-T-C

111729674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45777019-A-G

111729697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776998-A-G

111729723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776976-C-T

111729733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776965-G-C

111729733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776965-G-T

111729764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776936-T-A

111730081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776637-C-G

111730081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776637-C-T

111730175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776555-T-G

111730239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776266-T-C

111730308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776198-T-C

111730409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776100-G-T

111730496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45776020-G-A

111730556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45775981-C-T

111730741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45775810-A-G

111730747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45775804-A-T

111730805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45775734-G-T

111730829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45775703-T-A

111731185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45775224-G-T

111731284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45775064-T-C

111731344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45775007-G-T

111731880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45774437-T-G

111731936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45774385-A-T

111731982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45774338-G-T

http://identifiers.org/hco/3/GRCh38#111732329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45774033-C-A

111732329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45774033-C-T

111732340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45774022-T-C

111732369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45773991-T-C

111732369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45773991-T-G

111732481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773893-A-G

111732520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45773876-A-G

http://identifiers.org/hco/3/GRCh38#111732769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45773671-C-A

111732769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773671-C-T

111732793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773647-G-A

111732793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773647-G-C

111732793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773647-G-T

111732921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773517-G-A

111733076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773359-T-C

111733359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773126-T-G

111733384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773101-G-C

111733391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773094-C-G

111733391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773094-C-T

111733396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45773086-C-G

111733622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772860-G-A

111733816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772683-A-G

111733825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772674-C-T

111733938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772558-G-A

111734083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772412-A-G

111734120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772376-T-C

http://identifiers.org/hco/3/GRCh38#111734124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45772372-A-C

111734124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772372-A-G

111734166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772344-G-T

111734218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772288-G-T

111734247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772259-G-A

111734247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772259-G-C

111734274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772245-T-C

http://identifiers.org/hco/3/GRCh38#111734567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45772129-A-C

111734567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772129-A-G

111734645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772062-G-T

111734680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45772026-A-G

111734802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771891-A-G

111734982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771688-G-A

111735050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771632-T-C

111735099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771582-C-T

111735412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45771069-A-G

111735485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770896-A-G

111735680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770701-C-G

111735695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770684-A-G

111735913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770467-G-C

111735937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770443-C-T

111735969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770411-A-G

111736016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770366-T-A

111736130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770256-C-T

111736157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770229-T-C

111736348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45770058-G-A

111736521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769868-T-C

111736521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769868-T-G

111736619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769739-C-G

http://identifiers.org/hco/3/GRCh38#111736754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45769612-A-C

111736834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769539-T-G

111736876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769508-G-A

111737513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45769226-C-T

111737780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768927-T-C

111737909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768799-A-G

111737961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768747-A-T

111738121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768591-G-A

http://identifiers.org/hco/3/GRCh38#111738167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45768554-A-C

111738376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768376-C-T

111738382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768370-G-A

111738563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768185-T-A

111738563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768185-T-G

111738620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45768103-G-A

111739740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45765553-G-A

http://identifiers.org/hco/3/GRCh38#111739827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45765457-C-A

111739829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45765455-C-T

111740013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45765275-A-G

111740042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45765238-A-G

111740042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45765238-A-T

111740065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45764177-C-T

111740493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763861-G-A

111740532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763823-C-T

111740606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763752-A-G

111741254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763362-C-T

http://identifiers.org/hco/3/GRCh38#111741293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45763330-C-A

111741386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763238-T-C

111741789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763123-T-A

111741837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45763075-T-C

111742179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762743-C-G

111742954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762485-T-C

111743017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762428-G-A

111743102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762345-A-G

111743135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762312-G-C

111743260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762197-G-C

111743331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45762102-G-A

http://identifiers.org/hco/3/GRCh38#111743382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45762051-A-C

111743455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761979-T-G

111743514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761924-G-T

111743535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761906-A-T

111743594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761850-A-G

111743629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761821-T-C

111743775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761674-T-C

111743803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761647-G-C

111744082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45761364-T-C

111747139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45760147-T-C

111747825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45759424-T-C

http://identifiers.org/hco/3/GRCh38#111747837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45759412-C-A

111747933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45759340-T-G

111747993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45759270-G-C

111748226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45759053-T-C

111748427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758747-A-G

111748774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758381-G-A

111748774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758381-G-T

111748946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758317-C-T

111749022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758243-T-C

111749066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758199-T-A

111749066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45758199-T-C

111749405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45757698-G-A

http://identifiers.org/hco/3/GRCh38#111749467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45757636-C-A

111749549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45757554-T-C

111749763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45757335-T-C

111749880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45757219-A-T

111749881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45757218-T-C

111750378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45756730-T-C

111750418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45756697-G-T

111750967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45756125-T-A

111751158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755869-G-C

111751199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755835-G-A

111751446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755600-C-T

111751500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45755545-A-G

111752212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755143-G-A

http://identifiers.org/hco/3/GRCh38#111752218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45755137-A-C

111752246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755109-G-A

111752248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755107-C-G

111752250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45755105-G-C

111752449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45754186-G-T

111758874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753823-G-T

http://identifiers.org/hco/3/GRCh38#111758916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45753774-C-A

111758947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753749-C-T

111758965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753731-A-G

111758974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753722-C-T

111759551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753068-C-T

111759568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45753051-T-A

111759774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45752871-C-T

111759775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45752870-A-G

111759822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45752823-C-G

111760072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751888-G-C

111760365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751618-G-C

111760365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751618-G-T

111760803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751229-G-A

111760844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751200-G-C

111761288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45751091-G-T

111761338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45751039-G-T

111761394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750983-C-G

111761501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750879-A-G

111761638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750753-T-C

111761676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750715-C-T

111761796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750614-A-G

111761915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750493-A-G

111761984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750326-G-C

http://identifiers.org/hco/3/GRCh38#111761989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45750321-A-C

111761989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750321-A-G

http://identifiers.org/hco/3/GRCh38#111762049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45750285-C-A

111762049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750285-C-G

111762226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45750106-A-G

111762417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45749938-G-A

111762475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45749880-C-T

111763306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45749045-A-G

111763779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45748614-C-T

http://identifiers.org/hco/3/GRCh38#111764321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45748099-C-A

111764411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45748003-G-A

http://identifiers.org/hco/3/GRCh38#111764596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45747809-C-A

111764607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45747798-C-T

111764714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45747720-A-T

111764719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45747716-A-G

http://identifiers.org/hco/3/GRCh38#111764832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45747635-C-A

111764931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45747532-T-C

111764944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45747519-T-A

111765168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45747315-C-T

111765614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45746938-T-C

http://identifiers.org/hco/3/GRCh38#111765760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45746802-A-C

111765845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45746713-T-G

111766084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45746360-T-A

111767252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45746194-G-T

111767609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745859-A-G

111767617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745846-A-G

111767678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745806-A-G

111767976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745551-G-A

111768171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745358-T-G

111768288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45745248-A-G

http://identifiers.org/hco/3/GRCh38#111768322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45745214-A-C

111768798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45744741-T-C

111768864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45744676-T-C

111768867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45744673-T-A

111769366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45744167-A-G

111769379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45744154-C-T

111769736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45743819-C-G

111769828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45743721-A-G

111769945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45743334-A-G

111770439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742824-A-G

111770479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742787-G-A

111770941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742602-C-T

http://identifiers.org/hco/3/GRCh38#111770980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45742550-C-A

111771062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742487-T-C

111771086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742469-T-C

111771135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742421-A-T

111771151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742405-T-C

http://identifiers.org/hco/3/GRCh38#111771349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45742138-A-C

111771349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45742138-A-T

111771715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45741718-G-A

111772087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740706-T-C

111772110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740684-T-C

111772156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740642-C-T

111772205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740592-T-C

111772493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740250-C-T

111772509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740234-C-T

111772673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45740073-G-T

111772821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739970-G-C

111772873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739950-A-G

111772924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739902-C-T

111772977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739851-A-G

111772977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739851-A-T

http://identifiers.org/hco/3/GRCh38#111773047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45739792-A-C

111773117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45739727-T-C

111773523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45738752-C-T

http://identifiers.org/hco/3/GRCh38#111773617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45738657-C-A

111773817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45738493-T-C

111773845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45738454-C-G

111774131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45738183-G-A

111774131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45738183-G-T

111774535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45737806-C-T

111774551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45737790-G-C

111774794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45737534-T-C

111774836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45737492-G-A

111775264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45737129-G-T

111775694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45736370-A-G

111775800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45736246-C-T

111775829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45736217-T-C

http://identifiers.org/hco/3/GRCh38#111775841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45736205-A-C

111776293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45735752-G-A

111776478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45735668-C-T

111776643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45735528-G-C

111776812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45735362-T-A

111777443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45734831-A-G

111777484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45734788-A-G

111777484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45734788-A-T

http://identifiers.org/hco/3/GRCh38#111779936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45732613-C-A

111779985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45732564-T-A

111779985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45732564-T-C

111779985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45732564-T-G

http://identifiers.org/hco/3/GRCh38#111780006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45732543-C-A

http://identifiers.org/hco/3/GRCh38#111781244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45731820-A-C

111781244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45731820-A-G

111781344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45731735-C-G

111781458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45731631-A-G

111781683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45731419-A-G

http://identifiers.org/hco/3/GRCh38#111781707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45731395-C-A

111781717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45731385-C-T

111781798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron variant
orthologous variants: 45731302-G-T

111781933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45731164-G-A

111781966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, undefined
orthologous variants: 45731142-A-G

http://identifiers.org/hco/3/GRCh38#111784047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45730090-C-A

111784248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45729887-T-G

111784450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45729674-T-C

111786850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45725413-T-A

111786920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45725343-G-A

111786930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45725331-G-A

111786986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45725275-A-G

111787318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45722075-C-T

111787595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721840-G-A

111787595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721840-G-T

111787722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721713-A-G

http://identifiers.org/hco/3/GRCh38#111788213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45721232-A-C

111788213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721232-A-G

http://identifiers.org/hco/3/GRCh38#111788292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45721154-C-A

111788293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721153-T-C

111788297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45721149-T-C

111788447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45720991-A-G

111788800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45720723-G-T

111788890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45720626-C-T

http://identifiers.org/hco/3/GRCh38#111789080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45720465-C-A

111789473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45720064-A-T

111789506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45720014-C-T

111789526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719999-A-G

111789526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719999-A-T

111789722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719835-T-G

111790133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719397-C-T

111790236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719295-A-G

111790281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719249-G-A

111790462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719059-C-G

111790486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45719035-G-A

111790530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718991-C-G

111790530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718991-C-T

111791094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718215-A-G

111791094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718215-A-T

111791138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718163-G-A

http://identifiers.org/hco/3/GRCh38#111791280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45718069-C-A

111791324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718034-T-C

111791349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45718009-T-A

http://identifiers.org/hco/3/GRCh38#111792248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45717808-C-A

111792372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45717633-G-A

111792817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

111794592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45717432-T-C

111794771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45717279-T-C

111795373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45716776-C-T

111801682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45715148-C-T

111801862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45714966-C-T

http://identifiers.org/hco/3/GRCh38#111801934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45714917-A-C

111801939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45714912-T-G

111802205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45714680-C-T

111802250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45714635-C-T

111802294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45714585-C-T

111802358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45714541-C-G

http://identifiers.org/hco/3/GRCh38#111803036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#45713825-A-C

111803241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45713655-A-G

http://identifiers.org/hco/3/GRCh38#111807154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45711875-A-C

111807866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45711581-G-C

111808486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45710978-T-C

111808717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45710904-C-G

111809144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45710436-T-G

111810439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708441-C-T

111810481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708371-G-T

111810530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708270-C-T

111810567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45708195-T-C

111811235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45707079-C-T

111811359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706954-G-A

111811402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706912-G-A

111811430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706884-G-T

111811640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706694-C-T

111811653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706681-C-T

http://identifiers.org/hco/3/GRCh38#111811665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45706669-C-A

111811665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706669-C-T

111811666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706668-G-A

111811702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706574-C-T

111811874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706425-T-A

111811939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706385-C-T

111812062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706285-G-C

111812075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706272-T-A

111812116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706221-G-C

111812116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706221-G-T

111812193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706125-T-C

111812317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45706003-T-A

111812374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45705950-C-T

111812570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704964-C-T

111812776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704762-A-G

111812817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704720-G-A

111812945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704594-C-G

111812945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45704594-C-T

111813434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45703493-T-C

http://identifiers.org/hco/3/GRCh38#111813664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45703277-A-C

http://identifiers.org/hco/3/GRCh38#111813779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45703176-C-A

111813779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45703176-C-T

111819568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45703019-T-C

111821191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701719-C-T

111821198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701712-C-T

111821204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701706-T-C

111821502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701355-G-A

111821567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701317-A-G

111821646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701241-A-G

http://identifiers.org/hco/3/GRCh38#111821801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45701105-C-A

111821801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45701105-C-T

111822978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45699078-G-C

111823410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45698669-T-G

111823594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45698490-A-G

111823883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45698199-T-C

111823899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45698180-G-T

111824731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696654-T-C

111824918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696515-T-C

111824973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45696464-A-G

111825239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695898-A-T

111825255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695884-T-G

111825313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45695834-G-C

111826774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45693966-G-T

111826793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45693947-A-T

111826857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45693882-G-A

111827970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45692054-G-A

111828063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691968-G-A

http://identifiers.org/hco/3/GRCh38#111828615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45691474-C-A

111828615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691474-C-G

111828934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691335-C-T

111829120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691154-C-T

111829121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691153-A-G

111829252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45691036-G-A

111829993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690613-A-T

111830426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45690204-T-C

111831249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689905-A-G

111831389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689761-A-T

111831390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689760-T-C

111831429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689721-A-G

http://identifiers.org/hco/3/GRCh38#111831539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45689603-A-C

111831539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689603-A-G

111831690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45689453-C-T

111832174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45688940-C-T

111832304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45688851-T-C

111832318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45688837-A-G

111832322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45688833-C-T

111834633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687986-T-G

111834676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687943-G-C

111834731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687876-T-C

111834760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687850-A-G

111834761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687849-C-T

http://identifiers.org/hco/3/GRCh38#111834838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45687770-C-A

111834838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687770-C-T

111834997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687657-A-G

111835112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687479-C-T

111835214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687405-T-C

111835247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687372-G-A

111835364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687282-A-G

111835568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45687107-C-G

111835734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45686963-T-A

111835837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45686891-G-A

111835837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45686891-G-C

111835845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45686883-G-C

111836045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686705-T-C

111837221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686550-G-A

http://identifiers.org/hco/3/GRCh38#111837241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45686534-A-C

111837252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686523-G-A

http://identifiers.org/hco/3/GRCh38#111837293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45686479-A-C

111837293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686479-A-T

111837360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686418-A-G

111837431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45686350-T-A

111838692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45685952-T-G

111838891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45685816-C-T

111839207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45685509-A-T

http://identifiers.org/hco/3/GRCh38#111839303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45685442-A-C

111839421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45685343-T-A

http://identifiers.org/hco/3/GRCh38#111844450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45683137-A-C

111844450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45683137-A-T

111844542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682856-C-T

111844590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682775-C-T

111844641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682739-C-T

111844750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682629-T-C

111845479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682259-T-A

111845479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45682259-T-G

111845664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45680975-G-A

111845718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45680911-G-A

111845836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45680782-A-G

111845885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45680733-C-T

http://identifiers.org/hco/3/GRCh38#111845985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45680640-C-A

111845985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45680640-C-T

111845993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45680628-T-C

111846262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45679941-G-A

111846262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45679941-G-T

http://identifiers.org/hco/3/GRCh38#111846287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45679916-C-A

http://identifiers.org/hco/3/GRCh38#111846288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#45679915-A-C

111846412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26462
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45679792-T-C