http://identifiers.org/hco/6/GRCh38#109444123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41362964-C-A

109444123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41362964-C-T

http://identifiers.org/hco/6/GRCh38#109444315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41362776-C-A

109444315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41362776-C-T

109444647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41362699-C-T

109444784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41362602-T-C

109444847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41362539-G-T

109444864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41362522-A-G

109444883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41362504-C-T

109445074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41362316-G-A

109445074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41362316-G-T

109445268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41362044-T-A

109445268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41362044-T-C

109445308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41362004-G-A

109445315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41361997-C-T

109445554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41361735-G-T

109445603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41361688-G-A

109445661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41361629-A-G

109445667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41361623-G-A

109445667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41361623-G-T

http://identifiers.org/hco/6/GRCh38#109445682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41361610-C-A

109445732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41361566-G-A

109445732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41361566-G-T

109445799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41361452-T-G

109445811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41361440-T-A

109445811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41361440-T-C

109445900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41361398-G-A

109446131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41361257-G-T

109446142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41361243-G-A

109446142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41361243-G-T

109446149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41361236-G-A

109446212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41361173-G-T

109446342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41361043-G-A

109446342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41361043-G-T

http://identifiers.org/hco/6/GRCh38#109446346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41361039-C-A

109446369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 41361022-G-C

109446369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 41361022-G-T

109446599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41360894-G-A

109446600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41360893-A-T

109446604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41360889-C-T

109446658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41360836-C-G

http://identifiers.org/hco/6/GRCh38#109446659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41360835-C-A

109446659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41360835-C-T

109446797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41360711-G-A

109446805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41360703-G-A

109446815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41360702-C-T

109446877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41360662-G-A

109446877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41360662-G-T

109447189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41360410-A-G

109447227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 41360372-G-A

109447338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41360267-C-T

109447434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41360165-C-T

http://identifiers.org/hco/6/GRCh38#109447577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41360050-C-A

109447577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41360050-C-G

109447577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41360050-C-T

109447599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41360028-G-A

109447623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41360011-A-G

http://identifiers.org/hco/6/GRCh38#109447660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41359989-C-A

109447660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359989-C-G

109447660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359989-C-T

109447758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359897-T-C

109447759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359896-T-G

109447767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359890-C-T

109447775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359882-C-G

http://identifiers.org/hco/6/GRCh38#109447805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41359851-C-A

109447805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359851-C-T

109447879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41359792-G-A

109447944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41359730-G-T

http://identifiers.org/hco/6/GRCh38#109448179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41359649-C-A

109448179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359649-C-T

109448395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 41359433-T-C

109448396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41359432-G-A

109448396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41359432-G-T

109448418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359411-C-G

http://identifiers.org/hco/6/GRCh38#109448460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41359363-C-A

109448516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359148-G-A

109448516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359148-G-T

109448566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41359011-C-T

109448629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358881-C-G

109448667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358826-T-C

109448873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 41358604-G-T

109448909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358567-G-T

109449209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358405-G-A

109449209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358405-G-C

http://identifiers.org/hco/6/GRCh38#109449240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41358385-C-A

109449240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358385-C-T

http://identifiers.org/hco/6/GRCh38#109449275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41358360-C-A

109449275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358360-C-T

http://identifiers.org/hco/6/GRCh38#109449278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41358353-C-A

109449278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358353-C-T

109449296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358335-G-A

109449296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358335-G-T

109449315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358323-A-G

109449315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358323-A-T

109449523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358161-C-T

109449559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358126-T-C

109449560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358125-A-T

http://identifiers.org/hco/6/GRCh38#109449573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41358112-A-C

109449573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358112-A-G

http://identifiers.org/hco/6/GRCh38#109449584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41358098-C-A

109449646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358037-G-A

109449646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358037-G-C

109449646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41358037-G-T

109449649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41358029-G-A

109449815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357866-G-A

109449815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357866-G-T

109449896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357785-A-G

http://identifiers.org/hco/6/GRCh38#109449927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41357752-A-C

109449982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41357687-A-G

http://identifiers.org/hco/6/GRCh38#109450144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41357526-C-A

http://identifiers.org/hco/6/GRCh38#109450213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41357468-C-A

109450261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357411-C-T

http://identifiers.org/hco/6/GRCh38#109450337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41357348-C-A

109450337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41357348-C-T

109450357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41357328-C-T

109450560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41357125-G-A

109450607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357077-G-T

http://identifiers.org/hco/6/GRCh38#109450654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41357037-C-A

109450654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357037-C-T

109450672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357026-T-A

109450672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41357026-T-G

109450937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41356725-T-C

109450983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41356675-C-T

109451493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41356482-G-A

109451493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41356482-G-T

http://identifiers.org/hco/6/GRCh38#109451510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41356465-C-A

109451510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41356465-C-G

109451510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41356465-C-T

109451703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 41356276-G-A

109452060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41355941-G-A

109452122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41355893-G-A

109452122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41355893-G-T

http://identifiers.org/hco/6/GRCh38#109452188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41355828-C-A

109452188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41355828-C-T

109452237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41355777-G-A

109452368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41355646-G-A

109452506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355498-C-T

109452585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41355419-T-C

109452585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41355419-T-G

http://identifiers.org/hco/6/GRCh38#109452766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41355248-C-A

109452766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355248-C-T

109452782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355232-G-A

109452848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41355178-G-C

109453375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41354946-G-A

109453381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41354940-G-A

http://identifiers.org/hco/6/GRCh38#109453420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41354913-C-A

109453420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41354913-C-T

109453521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41354736-T-C

109453536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41354721-G-A

109453536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41354721-G-C

109453536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41354721-G-T

http://identifiers.org/hco/6/GRCh38#109453545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41354712-C-A

109454544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353697-G-T

109454591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353650-G-T

http://identifiers.org/hco/6/GRCh38#109454622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41353606-C-A

109454622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41353606-C-T

109454652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41353579-T-G

109454752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41353477-A-G

109454989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353246-G-A

109454989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353246-G-T

109455007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353241-G-A

109455007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353241-G-T

109455224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353022-G-C

http://identifiers.org/hco/6/GRCh38#109455244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41353004-C-A

109455246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41353002-G-C

http://identifiers.org/hco/6/GRCh38#109455522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41352745-C-A

109455522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41352745-C-T

109455528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41352739-G-A

109455528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41352739-G-T

109455593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41352669-A-G

109455593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41352669-A-T

109455617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41352645-G-A

109455617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41352645-G-T

http://identifiers.org/hco/6/GRCh38#109455658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41352614-C-A

109455658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41352614-C-T

109455681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41352572-G-A

109455681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41352572-G-T

http://identifiers.org/hco/6/GRCh38#109455682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41352571-C-A

109455682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41352571-C-T

109455696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41352557-G-A

109455807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41352456-G-A

109455840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352441-G-T

109455871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352416-G-A

109455871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352416-G-C

109455871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352416-G-T

http://identifiers.org/hco/6/GRCh38#109455891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41352396-C-A

109455891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41352396-C-G

109456049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, undefined
orthologous variants: 41352260-T-C

109456049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, undefined
orthologous variants: 41352260-T-G

109456098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, undefined
orthologous variants: 41352229-T-C

109456367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, undefined
orthologous variants: 41352029-G-A

109456379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron_variant, undefined
orthologous variants: 41352019-G-C

109456480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41351931-A-G

109456493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41351918-A-G

109456598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41351820-G-A

109456598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41351820-G-T

109456759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41351686-T-G

109456838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41351636-T-C

109456904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41351561-G-A

109457383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41351095-A-G

109457720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41351002-G-C

109457743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41350972-T-A

109457794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41350913-A-G

109458300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41350465-G-C

109458988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41350024-A-T

109459064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41349946-A-G

109459064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41349946-A-T

109459381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41349653-A-G

109459392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: intron variant
orthologous variants: 41349642-A-G

109460687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41345696-T-C

http://identifiers.org/hco/6/GRCh38#109460891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41345493-A-C

109463345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41344184-A-G

109463391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41344140-A-G

http://identifiers.org/hco/6/GRCh38#109463662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41343957-C-A

109464003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41342784-A-G

109464276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41342096-T-C

109464326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41342054-T-C

109464476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41341927-T-A

109464858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41341749-T-C

109464914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41341690-T-C

109465236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41341391-T-G

109465251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41341376-T-G

http://identifiers.org/hco/6/GRCh38#109465267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41341366-C-A

109465481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41341231-G-A

109465481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41341231-G-T

109465607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41341135-T-C

109465617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41341125-A-T

109465761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41341008-G-T

http://identifiers.org/hco/6/GRCh38#109465927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41340883-A-C

109465927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41340883-A-G

109465945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20619
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 41340865-G-T