http://identifiers.org/hco/1/GRCh38#26281359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133854877-A-C

http://identifiers.org/hco/1/GRCh38#26281360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133854876-A-C

26281365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854871-T-G

26281410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854826-T-G

http://identifiers.org/hco/1/GRCh38#26281471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133854766-C-A

26281471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854766-C-T

26281557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854697-G-C

26281721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854574-T-C

26281750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854548-T-A

26281876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854446-T-C

26281876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854446-T-G

http://identifiers.org/hco/1/GRCh38#26281890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133854434-C-A

26281890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854434-C-T

26281892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854432-G-A

26281909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854415-G-A

26281909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854415-G-T

26282013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854309-G-A

26282013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854309-G-T

26282022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854300-T-C

26282054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854262-G-C

26282103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854231-A-G

26282103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854231-A-T

26282111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854223-T-C

http://identifiers.org/hco/1/GRCh38#26282125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133854211-A-C

26282125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854211-A-G

26282149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854187-G-A

26282149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854187-G-T

26282176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854164-T-C

http://identifiers.org/hco/1/GRCh38#26282270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133854095-C-A

26282270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 3 prime UTR variant
orthologous variants: 133854095-C-T

26282313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133854074-G-A

26282313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133854074-G-C

26282313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133854074-G-T

26282324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133854063-G-T

http://identifiers.org/hco/1/GRCh38#26282327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133854060-C-A

26282404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133854043-A-G

26282404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 133854043-A-T

http://identifiers.org/hco/1/GRCh38#26282429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133854035-C-A

26282429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133854035-C-T

http://identifiers.org/hco/1/GRCh38#26282447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133854017-C-A

26282447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133854017-C-G

26282447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133854017-C-T

26282468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133853996-G-A

26282572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 133853892-G-A

26282622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133853842-G-A

26282705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133853759-C-G

26282877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133853576-C-T

26283416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133853115-G-A

26283677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133852876-G-A

26283882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133852698-G-A

26284315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133852303-T-C

26284350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133852275-G-A

http://identifiers.org/hco/1/GRCh38#26284548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133852076-C-A

26284556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133852068-G-A

http://identifiers.org/hco/1/GRCh38#26284789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#133851906-C-A

26284789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133851906-C-T

26284869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133851828-A-G

26284937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133851766-G-A

26284937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133851766-G-T

26284961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133851758-A-G

26285018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133851705-T-C

http://identifiers.org/hco/1/GRCh38#26285055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#133851653-A-C

26285055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133851653-A-G

26285055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133851653-A-T

http://identifiers.org/hco/1/GRCh38#26285120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#133851589-C-A

26285165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133851543-T-C

26285189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133851508-A-T

26285240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133851456-G-A

26285240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133851456-G-T

26285392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133851302-T-C

26285392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133851302-T-G

26285443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 133851248-G-A

http://identifiers.org/hco/1/GRCh38#26285574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133851119-C-A

26285614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133851070-G-A

26285614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133851070-G-T

http://identifiers.org/hco/1/GRCh38#26285772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133850953-C-A

26285772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133850953-C-T

26285784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133850938-G-A

26285784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133850938-G-T

26285886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133850849-G-C

26285999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133850739-G-A

26285999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133850739-G-T

http://identifiers.org/hco/1/GRCh38#26287030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#133849905-A-C

26287030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133849905-A-G

26287091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133849843-G-A

26287322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133849699-C-T

26287466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133849471-C-G

26287702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133849033-C-T

26288020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133848817-A-G

26288330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133848620-G-A

26288330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133848620-G-T

26288599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133848320-C-G

26288942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133847921-G-A

26289007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133847858-T-C

26289160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133847695-C-G

26289160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133847695-C-T

26289249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133847617-T-C

26289443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133847508-C-T

26289627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133847321-C-T

26289926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133847081-A-G

26290374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133846819-C-G

26290393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133846803-T-C

26291055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133846313-C-T

26291118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133846259-A-G

26291126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133846251-G-C

http://identifiers.org/hco/1/GRCh38#26291304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133846114-C-A

26291304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133846114-C-T

26291381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133846042-C-G

26291381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133846042-C-T

http://identifiers.org/hco/1/GRCh38#26291418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133846009-A-C

26291479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133845953-A-G

26291480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133845952-C-T

26291550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133845853-G-A

26291592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133845799-C-T

26291732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133845673-C-T

26291939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133845544-C-T

26292025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133845462-C-G

26292085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133845414-C-T

26292333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133845179-C-T

26293998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133843617-T-C

http://identifiers.org/hco/1/GRCh38#26294060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133843585-C-A

26294320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 133843351-A-G

26296573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133841063-G-A

26296589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133841047-G-A

26296827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840820-A-T

26296835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840812-G-A

26296835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840812-G-T

http://identifiers.org/hco/1/GRCh38#26296897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133840754-C-A

26296897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840754-C-T

26296954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133840707-A-G

http://identifiers.org/hco/1/GRCh38#26297022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133840639-C-A

26297052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840612-C-T

26297240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840444-G-T

26297324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840368-T-C

26297475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 133840230-T-C

26297496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840208-A-G

26297504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840200-A-G

26297511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840193-G-A

26297511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840193-G-T

26297576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840179-G-A

26297601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840154-T-A

26297601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840154-T-C

http://identifiers.org/hco/1/GRCh38#26297739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133840033-A-C

26297747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133840025-C-G

http://identifiers.org/hco/1/GRCh38#26297826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133839978-C-A

26297826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839978-C-G

26297826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839978-C-T

http://identifiers.org/hco/1/GRCh38#26297833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133839971-C-A

26297833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839971-C-T

26297855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839949-G-C

26297855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839949-G-T

26297860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839944-A-G

http://identifiers.org/hco/1/GRCh38#26298096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133839791-C-A

26298096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839791-C-T

26298120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839768-G-A

26298120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839768-G-C

26298120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839768-G-T

26298121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133839767-G-T

26300068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837669-C-T

26300168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837594-C-T

26300232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837539-G-A

26300322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837471-C-G

http://identifiers.org/hco/1/GRCh38#26300825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133837055-C-A

26300825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837055-C-G

26300825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837055-C-T

26300862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133837015-T-C

http://identifiers.org/hco/1/GRCh38#26301107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133836787-C-A

26301107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836787-C-T

26301114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836780-T-A

26301114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836780-T-C

26301119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836775-T-C

26301350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836721-A-T

26301562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836560-G-A

26301562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836560-G-T

26301611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836511-G-A

26301639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836484-T-C

26301704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 133836418-G-A

26301704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133836418-G-C

26301704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 133836418-G-T

26301806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836324-T-A

26301806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133836324-T-G

http://identifiers.org/hco/1/GRCh38#26301872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133836262-C-A

26302528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835922-C-T

26302531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835919-T-C

26302768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835702-G-A

26302768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835702-G-C

26302768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835702-G-T

26302789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835683-A-G

26302849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133835628-C-G

26302849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133835628-C-T

26302944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133835534-C-T

26302954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133835522-A-G

26303032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835461-G-A

26303032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835461-G-T

26303183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835371-G-A

26303183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835371-G-T

26303190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835364-A-G

26303229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835337-G-T

http://identifiers.org/hco/1/GRCh38#26303248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133835319-C-A

http://identifiers.org/hco/1/GRCh38#26303311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133835248-A-C

26303311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835248-A-T

26303317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133835242-A-G

26304155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834403-A-G

26304358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834224-C-T

http://identifiers.org/hco/1/GRCh38#26304387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133834196-C-A

26304387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834196-C-G

26304569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834048-G-A

26304569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834048-G-T

26304645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133834015-T-C

26304966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133833758-T-C

26306453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133830106-C-T

26306621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 133829929-C-T

26306691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5 prime UTR variant
orthologous variants: 133829860-G-A

http://identifiers.org/hco/1/GRCh38#26306718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#133829830-A-C

26306718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, undefined
orthologous variants: 133829830-A-G

26306718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, undefined
orthologous variants: 133829830-A-T

http://identifiers.org/hco/1/GRCh38#26306878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133829753-C-A

26306878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 133829753-C-G

26307164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron_variant, undefined
orthologous variants: 133829516-T-C

26307418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133829083-G-A

26307999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828721-G-A

26308021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828700-T-C

26308037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828684-C-T

26308057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828665-G-A

26308057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828665-G-T

26308136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828552-C-T

26308174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828516-G-A

26308204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828501-T-A

26308204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828501-T-G

26308233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828468-C-T

26308244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828457-G-C

http://identifiers.org/hco/1/GRCh38#26308245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133828456-C-A

26308245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828456-C-T

26308246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133828455-A-G

26311855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133827885-C-G

26311908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133827826-T-G

26312100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133827639-C-T

http://identifiers.org/hco/1/GRCh38#26312167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133827615-A-C

26312167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133827615-A-G

26312169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133827613-G-A

26312213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133827571-C-T

26317709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133822586-A-T

26317788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133822517-T-C

http://identifiers.org/hco/1/GRCh38#26317835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133822457-C-A

26317835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133822457-C-T

http://identifiers.org/hco/1/GRCh38#26317862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133822434-C-A

26317862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133822434-C-G

26317862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133822434-C-T

26317869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: intron variant
orthologous variants: 133822427-T-C

http://identifiers.org/hco/1/GRCh38#26318103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#133822199-C-A

26318103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133822199-C-G

26318103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133822199-C-T

26318157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133822135-G-A

26318282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133822030-G-A

26318282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133822030-G-C

26318326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30600
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133821993-A-G