30726300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115905316-A-G

30726416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115905199-A-G

30726457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115905165-C-T

30726464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115905152-G-A

30726464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115905152-G-C

30726570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115905064-T-C

30726602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115905032-G-T

30726633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904989-A-G

http://identifiers.org/hco/3/GRCh38#30726779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115904900-C-A

30726779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904900-C-T

30726854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904820-T-C

30726854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904820-T-G

30726876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904798-A-G

30726889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904789-A-G

http://identifiers.org/hco/3/GRCh38#30726907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115904771-C-A

30726935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904740-A-T

30727020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904644-G-A

http://identifiers.org/hco/3/GRCh38#30727046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115904617-C-A

30727076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904286-A-G

30727115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904248-G-A

30727117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904246-A-G

30727201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904145-C-T

30727391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904017-G-T

30727400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904007-A-G

30727406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115904001-A-G

30727420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115903987-G-A

30727420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115903987-G-C

http://identifiers.org/hco/3/GRCh38#30727424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115903983-A-C

30727424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115903983-A-G

30727756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115903660-C-T

30727776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115903640-T-A

30727776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115903640-T-C

http://identifiers.org/hco/3/GRCh38#30727851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115903578-A-C

30727919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115903509-A-G

http://identifiers.org/hco/3/GRCh38#30727953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115903476-C-A

30728045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115903379-T-C

30728084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115903340-A-G

30728084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3 prime UTR variant
orthologous variants: 115903340-A-T

30728115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115903309-G-T

30728116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115903308-G-C

30728116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115903308-G-T

30728152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115903273-A-G

30728219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115903203-C-T

30728220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115903202-C-T

30728235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115903186-G-A

30728236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 115903185-C-T

30728246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115903175-A-G

http://identifiers.org/hco/3/GRCh38#30728346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/9/GRCm39#115903075-C-A

30728346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115903075-C-G

30728346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115903075-C-T

30728352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115903069-G-A

http://identifiers.org/hco/3/GRCh38#30728365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115903056-C-A

30728422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 115902999-G-A

30728422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 115902999-G-T

30728425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115902996-G-C

30730618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115901929-C-T

30730924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115901627-C-G

http://identifiers.org/hco/3/GRCh38#30731028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115901534-C-A

30731141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115901382-G-A

30731184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115901337-G-A

30731240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115901222-G-A

30731240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115901222-G-T

30731249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115901159-G-A

30731495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115900738-C-G

30731600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115900642-C-T

http://identifiers.org/hco/3/GRCh38#30731642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115900595-C-A

30731801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115900426-A-G

30732033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115900221-A-G

30732094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115900166-A-G

http://identifiers.org/hco/3/GRCh38#30732127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115900132-C-A

http://identifiers.org/hco/3/GRCh38#30732151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115900107-C-A

30732151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115900107-C-T

30732267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115899989-G-A

30732390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115899864-G-A

30732451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115899803-C-T

30732613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115899639-T-A

30736537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115898795-T-G

30736541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115898791-T-C

30736860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115898443-T-C

30737103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115898239-T-C

30737170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115898170-C-T

30737197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115898149-G-A

30737806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115897552-T-C

30737944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115897409-A-G

30737992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115897360-C-T

30738168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115897185-G-A

30738196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115897158-T-A

30742431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894387-T-G

30742441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894379-C-G

30742453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894367-C-T

30742477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894330-T-G

http://identifiers.org/hco/3/GRCh38#30742604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115894203-C-A

30742612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894195-G-C

30742636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894180-A-T

30742669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894147-C-T

30742674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894142-C-T

30742698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894119-G-C

30742701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894113-G-A

30742719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894095-T-C

30742738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894075-T-C

30742744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115894069-A-G

30742775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115893961-C-T

http://identifiers.org/hco/3/GRCh38#30742802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115893924-C-A

30742812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115893905-A-T

30742925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115893788-A-G

30743011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115893702-T-C

30743056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115893664-C-T

30743094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115893627-G-T

30743157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115893565-A-G

30743181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115893541-C-T

http://identifiers.org/hco/3/GRCh38#30743233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115893489-C-A

30743233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115893489-C-T

30746574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115891798-A-T

30746754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115891633-A-G

30746795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115891608-T-A

30746818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115891590-C-T

30747037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115891145-G-A

30747075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115891111-G-A

30747075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115891111-G-T

http://identifiers.org/hco/3/GRCh38#30747205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115890992-C-A

30747216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115890984-G-A

30747232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115890968-T-C

http://identifiers.org/hco/3/GRCh38#30747238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115890964-A-C

30747238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115890964-A-G

30747238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115890964-A-T

30747364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115890742-A-G

30747388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115890718-G-A

30747634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115890443-A-G

http://identifiers.org/hco/3/GRCh38#30747884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115890160-C-A

30748205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115889877-G-A

30748205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115889877-G-T

30748209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115889873-T-G

30748289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115889802-T-C

30748573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115888997-A-G

30748637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115888934-T-G

30748710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115888864-A-G

30748760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115888814-G-A

30754263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115887140-A-G

30754285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115887119-C-G

30754285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115887119-C-T

30754396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115887004-G-A

30754439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115886957-G-C

30754515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115886895-T-C

30754812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115886618-A-G

30755024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115886335-T-C

30755236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115886097-T-G

30755239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115886094-T-C

30755280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115886045-G-A

30755291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115886034-T-G

30755427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115885129-A-G

30755473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115885070-C-T

30755554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115884986-T-C

30755563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115884976-A-T

30755609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115884933-G-A

30755617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115884925-A-G

30756812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115883633-C-G

30756816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115883629-T-C

30756824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115883621-C-T

30756934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115883525-A-G

30756970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115883491-G-A

30756973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115883488-A-G

30757076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115883327-G-A

30757373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115883049-G-A

30758059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115882206-C-T

30758080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115882184-T-C

30758081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115882178-A-G

30758104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115882158-C-G

30759728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115879739-A-G

30759995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115879513-A-G

http://identifiers.org/hco/3/GRCh38#30760190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115879315-C-A

30760198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115879286-A-T

30760334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115879106-T-C

30760360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115879080-G-A

30760360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115879080-G-C

30760585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115878792-C-G

30760604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115878773-A-G

http://identifiers.org/hco/3/GRCh38#30760655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115878672-A-C

30760685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115878638-T-C

30761017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115878287-T-C

http://identifiers.org/hco/3/GRCh38#30761123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115878173-C-A

30761123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115878173-C-T

30761226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115878066-G-A

30761298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115877990-C-T

30768467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115872019-A-T

30768541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871946-G-C

30768541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871946-G-T

30768544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871943-G-A

30768544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871943-G-T

30768548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871939-A-G

30768549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871938-G-C

30768569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871921-G-A

30768668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871833-C-G

30768734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871190-A-T

30768779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871148-T-C

30768874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115871068-C-G

30768945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115870997-A-G

30768975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115870966-G-T

30769110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115870832-T-C

30769170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115870774-T-C

30769179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115870762-C-T

http://identifiers.org/hco/3/GRCh38#30769199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115870742-C-A

30769199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115870742-C-T

30771737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115868559-C-G

30771748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115868548-A-G

30771779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115868508-T-C

30771797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115868490-C-T

30772251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115868085-C-T

30772550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115867825-T-C

30774365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115865170-C-G

30774479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115865066-A-G

30774479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115865066-A-T

30774542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115864996-T-C

http://identifiers.org/hco/3/GRCh38#30774663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115864864-C-A

30774896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115864672-G-A

30775041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115864537-G-A

30775066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115864509-A-T

30775075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115864497-G-A

30775191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115864388-C-T

http://identifiers.org/hco/3/GRCh38#30775259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115864337-C-A

30775259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115864337-C-T

30775375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115864195-G-A

30775476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115864136-C-T

30776545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115862482-T-G

30776555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115862476-T-A

30776701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115862336-T-C

30776921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115862150-T-A

30776953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115862117-T-C

30777112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115861974-A-T

30777383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115861699-G-A

30777383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115861699-G-T

30777397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115861685-A-G

30777503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115861608-G-C

http://identifiers.org/hco/3/GRCh38#30777823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115860315-C-A

30777823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115860315-C-T

30777830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115860308-G-C

http://identifiers.org/hco/3/GRCh38#30777891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115860233-C-A

30777891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115860233-C-G

30777920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115860204-C-T

http://identifiers.org/hco/3/GRCh38#30777929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115860195-A-C

30777937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115860187-T-C

30777971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115860130-A-G

30778034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115860057-G-T

http://identifiers.org/hco/3/GRCh38#30778073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115860006-C-A

30778073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115860006-C-G

30778105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859984-T-C

30778158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859917-T-C

30778231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115859844-G-A

30778231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115859844-G-C

30778231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 115859844-G-T

30778299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859771-T-C

http://identifiers.org/hco/3/GRCh38#30778367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115859701-C-A

http://identifiers.org/hco/3/GRCh38#30778377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115859691-A-C

30778377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859691-A-G

30778399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859665-T-A

30778399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859665-T-C

30778399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859665-T-G

30778402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859662-A-T

30778428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859640-T-A

30778428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859640-T-C

30778433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859635-T-C

30778473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115859612-A-G

30779381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115859046-A-G

30779468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115858945-A-G

http://identifiers.org/hco/3/GRCh38#30779479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115858932-C-A

30779479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115858932-C-G

30779728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115858700-T-C

30779749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115858666-A-G

30779767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115858648-T-C

http://identifiers.org/hco/3/GRCh38#30779778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115858637-C-A

30779778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115858637-C-T

30779925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115858490-G-A

http://identifiers.org/hco/3/GRCh38#30779939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115858477-A-C

30779939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115858477-A-G

30779939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115858477-A-T

30780045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115858410-T-C

30780470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115857983-C-T

30780927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115857242-G-A

http://identifiers.org/hco/3/GRCh38#30780949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115857220-A-C

30780949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115857220-A-G

http://identifiers.org/hco/3/GRCh38#30780958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115857206-A-C

http://identifiers.org/hco/3/GRCh38#30780999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115857165-C-A

30780999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115857165-C-T

http://identifiers.org/hco/3/GRCh38#30781084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115857082-C-A

30781103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115857061-G-A

30781110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115857055-T-C

30781560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115856721-T-C

30781739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115856066-C-T

http://identifiers.org/hco/3/GRCh38#30781910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115855891-A-C

30782135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115855508-G-A

30782197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115855434-C-G

30782242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115855391-G-C

30782242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115855391-G-T

30782275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115855357-G-A

30782447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115855230-G-T

30782721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115854981-G-T

30782993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115854744-G-T

30783086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115854583-C-T

http://identifiers.org/hco/3/GRCh38#30783095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115854573-A-C

30783122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115854547-C-T

30783605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115854025-G-T

http://identifiers.org/hco/3/GRCh38#30783691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115853939-C-A

30783691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115853939-C-T

30783765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115853488-A-T

30783833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115853427-T-C

30783929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115853327-C-T

30783982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115853270-C-T

http://identifiers.org/hco/3/GRCh38#30785793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115852118-A-C

30785793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115852118-A-G

http://identifiers.org/hco/3/GRCh38#30785858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115851373-A-C

30785916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115851318-G-A

30785918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115851316-A-G

30785918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115851316-A-T

30786209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115851036-T-C

30786220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115851025-G-C

30786220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115851025-G-T

30786311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850940-C-T

30786313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850938-G-A

30786313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850938-G-C

30786313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850938-G-T

30786392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115850860-T-C

30786495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850733-G-A

30786495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850733-G-T

http://identifiers.org/hco/3/GRCh38#30786496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115850732-C-A

30786496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850732-C-T

30786505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850723-A-G

30786584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850655-G-T

30786612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850628-T-C

30786612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115850628-T-G

30791343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115847669-T-C

30791460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115847517-G-A

30791501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115847478-T-C

30791514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115847465-C-T

30791624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115847369-T-C

30792799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115846432-A-G

30793233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115846002-A-G

http://identifiers.org/hco/3/GRCh38#30793299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115845947-C-A

30793347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115845904-T-C

http://identifiers.org/hco/3/GRCh38#30793443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115845845-A-C

30793525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115845779-T-C

30793619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115845676-G-A

30793881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115845119-T-C

30793950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115845048-A-T

30793968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115845031-A-G

30794417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115842941-A-G

30794440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115842919-T-C

30794556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115841754-C-T

30794598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115841712-A-G

30794611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115841699-A-G

30794749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115841577-C-T

30794759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115841567-G-C

30795777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115839791-G-T

http://identifiers.org/hco/3/GRCh38#30796050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115839494-C-A

30796050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115839494-C-T

30796247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115839297-C-G

30796308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115839240-C-T

30800800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115835827-C-T

30800877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 115835777-A-G

30800985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115835668-C-T

http://identifiers.org/hco/3/GRCh38#30801048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115835605-A-C

http://identifiers.org/hco/3/GRCh38#30801153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115835505-C-A

30801153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115835505-C-T

30801527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115835133-G-A

30801553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115835120-G-C

30801586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115835083-G-T

30806281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115832797-A-G

30806299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115832793-A-G

30806377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115832719-G-T

30806389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115832707-A-G

30806724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831865-G-A

30806734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831855-A-G

30806737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831852-T-G

30806769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831801-C-T

30806906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831669-C-T

30807184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831429-C-T

30807281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831335-A-G

30807361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831274-C-T

30807445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831172-A-G

30807460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831157-T-C

30807523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115831101-A-T

30808944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115829650-T-G

http://identifiers.org/hco/3/GRCh38#30808950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115829644-C-A

30808950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115829644-C-T

30808969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115829627-T-C

30809077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115829525-C-G

30809078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115829524-T-C

30809084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115829518-C-T

30809091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115829511-G-A

30809231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115829374-G-A

30809341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115829260-T-G

30810019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115829043-T-C

30810276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115828794-G-A

30810287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115828778-T-C

http://identifiers.org/hco/3/GRCh38#30810441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115828694-C-A

30810441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115828694-C-T

30810463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115828672-G-A

http://identifiers.org/hco/3/GRCh38#30810803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115828403-C-A

30810933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115828066-G-A

30810933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115828066-G-T

30811202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115827843-A-G

30811219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115827826-G-T

30811238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115827807-G-C

30811798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115827262-T-A

30811798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115827262-T-C

30811872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115827183-G-A

30811901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115827152-T-A

30811981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115827028-T-G

30812848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115825678-T-C

30813104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115825489-T-C

30813207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115825375-C-T

30813823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115824574-A-G

30813986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115824403-T-C

http://identifiers.org/hco/3/GRCh38#30814253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115824169-C-A

30814261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115824161-A-G

30814316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115824107-A-G

http://identifiers.org/hco/3/GRCh38#30814976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115823490-A-C

30815023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115823436-T-A

30815109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115823354-T-C

http://identifiers.org/hco/3/GRCh38#30815128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115823335-A-C

30815146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115823318-G-C

30815227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115823253-C-T

30815325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115822927-T-A

30815325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115822927-T-C

30815500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115822760-T-C

30815515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115822746-G-A

30815534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115822729-A-G

30815678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115822589-C-G

30815822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115822510-T-A

30815850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115822471-C-G

30816913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821889-T-C

30816915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821887-G-A

30816966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821833-A-G

30816970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821829-C-T

30816978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821821-G-A

30817012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821787-G-A

30817040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821750-T-G

http://identifiers.org/hco/3/GRCh38#30817114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115821710-A-C

30817114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821710-A-G

30817127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821701-A-G

30817301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821526-G-A

30817303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821524-T-C

30817379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115821453-A-G

30818110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115820811-C-T

30818981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115819573-C-G

30818981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115819573-C-T

http://identifiers.org/hco/3/GRCh38#30819024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115819528-C-A

30819038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115819510-T-C

30819178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115819355-T-A

30819243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115819301-C-T

http://identifiers.org/hco/3/GRCh38#30819266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115819282-C-A

30819266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115819282-C-T

30819294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115819251-T-A

30819406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115819150-A-G

30819770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115818789-A-G

30820503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115816909-G-A

30823033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115813287-G-A

30823316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115813026-T-C

30823356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115812989-A-G

30823454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115812893-T-C

30823503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115812844-T-C

http://identifiers.org/hco/3/GRCh38#30823516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115812831-C-A

30823516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115812831-C-T

30825180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115808216-G-A

30825180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115808216-G-C

30825238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115808190-T-A

30826481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115807238-T-A

30826673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115807042-G-A

30826729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115806983-A-G

30826733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115806979-A-T

http://identifiers.org/hco/3/GRCh38#30827416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115806153-C-A

30828445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115804268-C-T

30828447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115804266-T-A

30828448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115804265-T-C

30828456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115804257-T-C

http://identifiers.org/hco/3/GRCh38#30829030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115802629-C-A

30829400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115802208-T-C

30829420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115802186-T-C

30829598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115802015-G-C

http://identifiers.org/hco/3/GRCh38#30832009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115797491-C-A

30832009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115797491-C-T

http://identifiers.org/hco/3/GRCh38#30832121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115797378-A-C

http://identifiers.org/hco/3/GRCh38#30832261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115797244-A-C

30832409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115797097-T-A

30832746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115796758-A-G

30832771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115796732-C-T

30832924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115796309-A-G

30833415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115795809-T-A

30833603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115795624-G-C

30833807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115795431-G-T

http://identifiers.org/hco/3/GRCh38#30833817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115795421-C-A

30833817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115795421-C-T

30833890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115795352-C-G

30833973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115795271-C-G

30833973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115795271-C-T

30834080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115795179-A-G

30834101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794925-T-C

30834101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794925-T-G

30834115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794855-A-G

30834132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794838-T-A

http://identifiers.org/hco/3/GRCh38#30834152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115794811-C-A

30834152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794811-C-T

30834177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794777-C-T

30834304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794648-A-G

30834578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794397-C-G

30834803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794163-A-G

30834828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794140-G-T

30834891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115794063-A-G

30835060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115793893-A-G

30835063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115793890-T-G

30835177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115793759-G-A

30835177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115793759-G-C

30835254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115793683-G-A

30835464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115793476-T-C

30835554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115793394-T-C

30835590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115793358-G-A

30835605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115793342-G-A

http://identifiers.org/hco/3/GRCh38#30835681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115793266-C-A

30835962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115793105-A-G

http://identifiers.org/hco/3/GRCh38#30836255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115792964-C-A

http://identifiers.org/hco/3/GRCh38#30836258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115792961-C-A

30836334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792905-A-T

30836379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792869-A-G

http://identifiers.org/hco/3/GRCh38#30836395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115792853-C-A

30836395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792853-C-T

30836456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792770-C-T

30836458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792768-T-C

http://identifiers.org/hco/3/GRCh38#30836554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115792677-A-C

30836554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792677-A-G

30836557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792674-T-C

30836563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792668-G-A

30836567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792664-C-T

30837259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792094-C-G

30837259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792094-C-T

30837299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792054-C-T

30837300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792053-C-T

30837308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115792045-A-G

http://identifiers.org/hco/3/GRCh38#30837353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115791997-A-C

30837436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115791871-G-T

30837552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115791758-C-T

http://identifiers.org/hco/3/GRCh38#30837669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115791678-A-C

http://identifiers.org/hco/3/GRCh38#30838017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115791342-A-C

30838253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115791096-A-G

30838731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789789-A-G

30838784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789735-T-A

30838854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789669-G-A

30838917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789614-T-C

30838954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789589-A-G

30838980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789556-C-T

30839061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115789475-G-A

30839061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115789475-G-T

30839134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789400-C-T

30839185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789349-A-G

30839211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789334-A-G

30839211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789334-A-T

30839212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789333-T-C

30839212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789333-T-G

30839227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789318-G-A

30839227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789318-G-T

30839322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789221-T-C

30839332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789211-T-C

30839473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789049-A-G

30839494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115789028-T-G

30839816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115788719-T-C

30839908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115788063-C-T

30840139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115787904-G-A

30840705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115787330-G-A

30840835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115787201-G-A

30840854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115787182-A-G

30841055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115786984-G-A

http://identifiers.org/hco/3/GRCh38#30841095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115786949-C-A

30841157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115786888-G-A

30841157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115786888-G-C

30841584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115786248-C-T

30841738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115786104-T-C

http://identifiers.org/hco/3/GRCh38#30841801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115786045-C-A

30841897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115785958-A-G

30841898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115785957-T-A

30841898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115785957-T-C

http://identifiers.org/hco/3/GRCh38#30842175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115785634-A-C

30842271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115785537-T-G

30842469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115785371-G-T

30842474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115785366-T-G

30842517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115785324-G-A

30842616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115785138-C-T

http://identifiers.org/hco/3/GRCh38#30842786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115784944-C-A

30842786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784944-C-T

http://identifiers.org/hco/3/GRCh38#30842850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115784878-C-A

30842850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784878-C-T

30842877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784851-A-T

30842881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784847-T-C

30842936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784819-C-T

30842964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784799-G-A

30843563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784311-A-G

30843611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784272-G-T

30843668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784205-G-T

30844014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784053-G-A

30844014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784053-G-C

http://identifiers.org/hco/3/GRCh38#30844015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115784052-C-A

http://identifiers.org/hco/3/GRCh38#30844087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115784001-C-A

30844087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115784001-C-T

30844094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783994-T-A

30844094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783994-T-C

30844100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783988-T-C

30844111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783976-G-A

30844111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783976-G-T

30844124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783963-C-T

30844165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783940-G-A

30844165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783940-G-T

http://identifiers.org/hco/3/GRCh38#30844170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115783935-C-A

30844170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783935-C-T

http://identifiers.org/hco/3/GRCh38#30844176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115783929-C-A

30844176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783929-C-G

30844176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783929-C-T

http://identifiers.org/hco/3/GRCh38#30844184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115783924-C-A

30844184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783924-C-T

30844235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115783878-T-C

30844235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115783878-T-G

30844289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783824-T-C

30844318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783795-G-A

30844318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783795-G-T

30844348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783768-C-G

30844348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783768-C-T

30844353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783761-C-T

30844462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115783642-T-A

30844462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115783642-T-C

http://identifiers.org/hco/3/GRCh38#30844513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115783595-C-A

30844518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783590-A-G

30844535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783573-A-G

30844606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783489-A-G

http://identifiers.org/hco/3/GRCh38#30844616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115783479-C-A

30844616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783479-C-G

http://identifiers.org/hco/3/GRCh38#30844763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115783369-C-A

30844763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783369-C-G

30844763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783369-C-T

30844902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783250-T-C

30844948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783206-T-C

30845012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115783153-G-A

http://identifiers.org/hco/3/GRCh38#30845043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115783122-C-A

30845195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115782738-A-G

30845223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115782713-C-G

30845223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115782713-C-T

30845313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115782624-C-T

http://identifiers.org/hco/3/GRCh38#30845410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115782529-C-A

http://identifiers.org/hco/3/GRCh38#30845418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115782521-A-C

30845625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115782307-A-G

30845874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115782056-T-C

30846000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115781923-C-T

30846009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115781914-C-T

http://identifiers.org/hco/3/GRCh38#30846068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115781860-A-C

30846124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115781805-C-T

30846161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115781768-A-T

30846583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115781409-A-T

http://identifiers.org/hco/3/GRCh38#30846747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115781240-C-A

30846918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115780653-C-T

30846931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115780641-C-T

http://identifiers.org/hco/3/GRCh38#30847274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115780303-A-C

http://identifiers.org/hco/3/GRCh38#30847292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115780284-C-A

30847329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115780247-C-T

30847330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115780246-T-C

30847362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115780214-G-A

30849803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778899-A-T

30849864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778818-A-G

http://identifiers.org/hco/3/GRCh38#30849909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115778772-C-A

30849909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778772-C-T

30850189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778484-T-A

30850189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778484-T-C

30850189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778484-T-G

http://identifiers.org/hco/3/GRCh38#30850191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115778482-A-C

30850242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778431-A-G

30850312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778377-T-C

30850525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778149-C-G

30850582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778092-T-C

30850589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115778085-G-A

30850763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115777905-G-T

30850802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115777864-G-A

30850802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115777864-G-T

30850888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115777778-T-C

30851063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115777599-A-T

http://identifiers.org/hco/3/GRCh38#30851091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115777572-C-A

30851091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115777572-C-T

http://identifiers.org/hco/3/GRCh38#30851354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115777341-A-C

30851477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115777233-G-T

30851500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115777210-C-G

30851544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115777184-C-G

30851544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115777184-C-T

30851984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115776760-G-T

30852318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115776534-C-T

http://identifiers.org/hco/3/GRCh38#30852609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115776459-C-A

30852620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115776448-A-G

30852623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115776445-T-C

30852893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115776205-G-A

30852893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115776205-G-C

30853117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115775973-A-G

30853407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115775732-C-T

30854519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115773465-G-A

30854586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115773401-G-T

30854590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115773397-T-C

30854663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115773347-A-T

30854806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115773221-G-A

30854806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115773221-G-C

30854806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115773221-G-T

http://identifiers.org/hco/3/GRCh38#30854826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115773201-A-C

http://identifiers.org/hco/3/GRCh38#30854868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115773184-C-A

30854868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115773184-C-G

30854889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115773180-C-T

http://identifiers.org/hco/3/GRCh38#30854890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115773179-A-C

30854891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115773178-C-T

30855238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115772502-G-T

http://identifiers.org/hco/3/GRCh38#30855249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115772491-C-A

30855293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115772451-T-C

30855335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115772410-A-G

30855452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115772353-G-A

30855503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115772303-G-A

30855504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115772302-G-T

30855691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115772089-T-C

http://identifiers.org/hco/3/GRCh38#30855914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115771883-C-A

30855914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115771883-C-G

30855914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115771883-C-T

30856109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115771687-G-A

http://identifiers.org/hco/3/GRCh38#30856184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115771612-C-A

30856330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115771455-C-T

30856398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115771334-C-T

30856500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115771070-T-C

http://identifiers.org/hco/3/GRCh38#30856750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115770711-A-C

30856871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770596-G-A

30856871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770596-G-C

30856871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770596-G-T

30856921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770542-T-C

http://identifiers.org/hco/3/GRCh38#30856935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115770528-C-A

30856935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770528-C-T

30856938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770525-T-C

30856975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770503-G-A

30856975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770503-G-C

30856975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770503-G-T

30857124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: synonymous variant
orthologous variants: 115770357-A-G

30857189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770287-A-G

30857209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770267-G-A

30857209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770267-G-T

30857222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770246-T-C

http://identifiers.org/hco/3/GRCh38#30857254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115770213-C-A

30857254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770213-C-G

30857459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115770046-G-C

http://identifiers.org/hco/3/GRCh38#30857628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115769879-C-A

30857628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769879-C-T

30857755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769750-C-T

30857773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769733-T-C

30858010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769528-T-C

30858197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769346-T-C

30858288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769329-G-T

30858302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769315-C-T

30858320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769312-A-G

30858344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769288-G-A

30858506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769270-G-A

30858506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769270-G-T

30858847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769067-C-G

30858896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115769024-G-A

30859122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115768800-G-A

30860073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115768138-A-G

30860087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115768124-T-C

30860616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115766815-T-C

30860847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115766577-G-C

30861784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115766187-A-G

30861785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115766186-T-C

30861788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115766183-T-C

30861811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115766158-A-G

30861811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115766158-A-T

http://identifiers.org/hco/3/GRCh38#30861849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115766089-C-A

30861868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115765992-C-G

30861912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115765947-T-G

30862000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115765884-A-G

30862238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115765658-C-T

http://identifiers.org/hco/3/GRCh38#30862298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115765601-C-A

30862348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115765536-T-G

30862352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115765423-T-G

30862664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115765065-T-G

30862697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115765036-C-T

30862758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115764975-C-T

30862796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115764935-T-C

30862828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115764903-C-T

30862860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115764871-A-G

30862964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115764776-C-T

30863299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115763636-A-G

30863538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115763412-G-A

30863674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115763274-C-T

http://identifiers.org/hco/3/GRCh38#30863702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115763247-A-C

30863702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115763247-A-G

30863735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115763219-G-C

30863735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115763219-G-T

30863750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115763202-C-T

30863859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115762962-A-G

30863866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115762955-T-C

http://identifiers.org/hco/3/GRCh38#30863925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115762915-C-A

30863941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115762898-G-C

30864012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115762827-A-G

30864416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115762465-A-G

30864437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115762444-T-C

30864481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115762403-A-T

http://identifiers.org/hco/3/GRCh38#30864505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115762379-A-C

30864764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115762156-G-A

30864894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115762052-C-T

30864991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115761982-A-G

30865022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115761949-A-G

30865027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115761944-C-T

30865085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115761876-T-A

30865156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115761807-A-G

30865160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115761803-C-T

30865167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115761796-T-C

30865210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115761756-C-G

30871273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115759645-A-T

30871290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115759628-G-C

30871339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115759578-G-A

http://identifiers.org/hco/3/GRCh38#30871348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115759569-C-A

30871421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115759532-C-G

30871421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115759532-C-T

30871515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115759460-C-T

30871558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115759416-C-G

30871558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115759416-C-T

30871766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115759196-C-G

30871852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115759122-C-T

http://identifiers.org/hco/3/GRCh38#30872624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115756898-A-C

30872704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115756825-T-A

30872704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115756825-T-C

30872705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115756824-T-A

30872758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115756769-T-C

30873146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115756321-C-T

30873170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115756296-T-C

30873519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115755652-C-T

30873864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115755305-T-C

30873904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115755259-G-C

30873978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115755182-A-T

30874067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115755106-C-G

30874140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115755056-G-A

30874140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115755056-G-C

30874140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115755056-G-T

30874325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115754887-C-T

30874344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115754868-T-C

http://identifiers.org/hco/3/GRCh38#30874375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115754842-C-A

30874515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115754711-A-G

30874542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115754684-T-C

30874734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115754386-G-A

30875205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115753923-G-A

30875207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115753921-T-A

30875243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115753897-G-T

30875288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115753856-G-A

30875332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 115753812-A-T

30875795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115753370-G-C

30875798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115753367-A-G

30877335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115752305-C-T

30877365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115752275-T-C

30877605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115752021-T-C

http://identifiers.org/hco/3/GRCh38#30877620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115752007-A-C

30877620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115752007-A-G

30877663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115751964-T-G

30877749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115751805-G-C

30877759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115751795-T-C

30877954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115751522-T-C

30878081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115751302-T-C

30878144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115751206-G-A

30878226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115751123-T-C

30879387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115750195-C-T

30881011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115747967-C-T

30881339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115747674-A-T

30881375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115747634-A-T

http://identifiers.org/hco/3/GRCh38#30881403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115747611-C-A

30881403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115747611-C-T

30884671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115746147-G-A

30884820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115746002-G-T

30885080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115745378-T-C

30885253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115745209-C-G

30885253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115745209-C-T

30885275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115745190-T-C

30885434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115745023-T-G

30885681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115744764-T-C

30886197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115744383-T-G

30886390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115744208-C-T

30886417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115744199-C-T

30886468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115744177-A-T

30886519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115744128-G-A

30886824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743610-G-A

30886859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743579-A-G

30886928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743516-A-G

30886948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743494-G-C

30889436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743347-C-T

30889440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743343-C-T

30889455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743328-A-T

30889545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743231-A-G

30889582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743195-A-T

30889625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743157-T-A

30889625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115743157-T-G

30889933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115742639-T-C

30890995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115741463-T-A

30891098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115741365-G-C

http://identifiers.org/hco/3/GRCh38#30891136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115741328-C-A

30891203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115741266-A-G

30891460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115741100-C-T

30891567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115740997-G-C

30891761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115740862-C-T

30891906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115740264-T-C

30892090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115740060-T-C

http://identifiers.org/hco/3/GRCh38#30893868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115738371-C-A

http://identifiers.org/hco/3/GRCh38#30893989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115738256-A-C

30894222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115737979-C-T

30894396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115737828-A-G

30894433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115737798-A-G

http://identifiers.org/hco/3/GRCh38#30894457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115737774-C-A

30894457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115737774-C-T

30894460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: intron variant
orthologous variants: 115737771-A-T

30894598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115737649-T-A

http://identifiers.org/hco/3/GRCh38#30894599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115737644-C-A

30894599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115737644-C-T

30894604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: missense variant
orthologous variants: 115737640-T-C

30894616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 5 prime UTR variant
orthologous variants: 115737628-T-C

http://identifiers.org/hco/3/GRCh38#30894617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27949
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#115737627-C-A