119557217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54702428-T-C

119557236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54702447-A-G

http://identifiers.org/hco/8/GRCh38#119557334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54702545-A-C

119557340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54702551-C-T

119557513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54702754-T-G

119557607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54702848-G-A

119557611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54702852-G-A

119557698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54702939-T-A

119557698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54702939-T-C

http://identifiers.org/hco/8/GRCh38#119557718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54702951-A-C

119557718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54702951-A-T

http://identifiers.org/hco/8/GRCh38#119557721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54702954-C-A

119557755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54702986-G-A

119557755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54702986-G-T

http://identifiers.org/hco/8/GRCh38#119557831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54703029-C-A

http://identifiers.org/hco/8/GRCh38#119557832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54703030-C-A

119557832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54703030-C-T

119557988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54703185-G-A

119558048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54703244-A-G

119558256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54703437-C-T

119558261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54703442-G-A

119558499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54703688-T-G

119558647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54703842-T-C

119558866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54704060-C-T

119559094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54704271-C-T

119559255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54704421-G-C

119559411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54704574-G-C

119559548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54704696-G-A

119559880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54705264-G-A

119560099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54705484-C-G

119560099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54705484-C-T

119560135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54705507-C-T

119560168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54705540-C-G

119560334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54705693-T-C

119560698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54706034-G-A

119560799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54706097-T-C

http://identifiers.org/hco/8/GRCh38#119560869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54706149-C-A

119561039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54706331-T-A

http://identifiers.org/hco/8/GRCh38#119561048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54706338-C-A

119561048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54706338-C-G

119561048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54706338-C-T

119561513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54706817-G-A

119561554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54706860-C-T

119561555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54706861-C-T

http://identifiers.org/hco/8/GRCh38#119562718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54707654-C-A

119562734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54707670-T-A

119562734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54707670-T-C

http://identifiers.org/hco/8/GRCh38#119562756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54707700-C-A

119562756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54707700-C-T

119562786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54707725-T-C

119562884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54707802-G-A

119562884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54707802-G-T

119562935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54707853-A-T

119563348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54708222-G-T

119563523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54708375-A-G

119563594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54708430-C-T

119563683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54708520-T-C

119563964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54708749-G-A

119564018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54708764-A-T

119564129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54708825-C-T

119564195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54708891-T-G

119564317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54709012-A-G

http://identifiers.org/hco/8/GRCh38#119564360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54709049-C-A

119564360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54709049-C-T

119564697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54709112-T-A

119564697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54709112-T-C

119564697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54709112-T-G

119564857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54709243-C-T

119564858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 54709244-A-G

119564858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 54709244-A-T

119565033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54709411-C-T

119565187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54709541-G-A

119568095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54710567-A-G

119568102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54710574-G-T

119568144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54710614-T-A

119568144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54710614-T-C

119568358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54710814-T-C

119568362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54710818-G-A

119568362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54710818-G-C

119568362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54710818-G-T

119568402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54710859-T-C

119568402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54710859-T-G

119568958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54711265-C-G

http://identifiers.org/hco/8/GRCh38#119568969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54711276-A-C

119569045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54711342-T-C

http://identifiers.org/hco/8/GRCh38#119569157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54711437-C-A

119569210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54711545-T-C

119569266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54711602-C-T

http://identifiers.org/hco/8/GRCh38#119569311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54711647-A-C

119569397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54711733-A-G

119569411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54711739-G-T

119569553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54711869-C-T

119569645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54711990-A-G

119570309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54712887-G-A

119570309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54712887-G-C

119570326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54712892-T-A

119570326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54712892-T-G

119570341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54712907-G-C

119570458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54713007-A-G

119570559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54713104-T-C

http://identifiers.org/hco/8/GRCh38#119570590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54713177-C-A

119570608-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54713202-T-A

119570608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54713202-T-C

119570630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54713280-T-C

http://identifiers.org/hco/8/GRCh38#119570658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54713316-A-C

119570658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54713316-A-G

119570664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54713344-G-A

119570664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54713344-G-T

119570726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54713408-T-C

119570737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54713419-G-A

119570737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54713419-G-C

119570737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 54713419-G-T

http://identifiers.org/hco/8/GRCh38#119570889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54713573-C-A

119570889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54713573-C-G

119570889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54713573-C-T

119571003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54713683-T-G

119571005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54713685-T-A

119571061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54713725-G-A

119571061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54713725-G-T

119571187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54713823-C-T

119571455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714054-T-C

119571462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714060-C-G

119571533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714115-A-T

119571610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714192-A-G

119571644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714227-G-T

119571689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714264-A-G

http://identifiers.org/hco/8/GRCh38#119571690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54714265-C-A

119571690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714265-C-G

119571715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714290-G-T

119571930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714498-A-G

119571930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714498-A-T

http://identifiers.org/hco/8/GRCh38#119572022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54714590-C-A

119572022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714590-C-T

119572044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714612-A-G

119572052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714620-G-T

119572204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54714772-G-A

119572204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54714772-G-T

119572265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54714833-A-G

http://identifiers.org/hco/8/GRCh38#119572274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54714842-C-A

119572274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54714842-C-G

119573470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54716463-T-A

119574170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54716816-G-C

http://identifiers.org/hco/8/GRCh38#119574185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54716829-C-A

119574185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54716829-C-G

119574214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54716856-G-A

119574360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54717005-G-A

119574389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54717762-G-A

119574789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54718160-A-G

119574806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54718194-T-A

119574806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54718194-T-C

119574806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54718194-T-G

119574807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54718195-G-A

http://identifiers.org/hco/8/GRCh38#119574898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54718496-C-A

119575099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54718691-T-C

119575167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54718762-G-A

http://identifiers.org/hco/8/GRCh38#119575257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54718832-A-C

119575257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54718832-A-T

119575621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54719123-A-G

119575650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54719149-A-G

119575901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54719389-T-C

119576076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54719552-C-T

119576461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54719608-A-G

119576485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54719632-A-G

http://identifiers.org/hco/8/GRCh38#119576508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54719652-A-C

119576508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54719652-A-T

119576726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54719835-C-T

119576730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54719839-C-T

119577120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54720212-G-A

119577124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54720216-C-G

119577124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54720216-C-T

119577162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54720244-A-T

119577355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54720444-G-A

119577654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54720702-T-C

119577654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54720702-T-G

http://identifiers.org/hco/8/GRCh38#119577907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54721276-C-A

119577907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54721276-C-T

119577911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54721280-C-T

119577969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54721327-G-A

119578396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54721409-A-G

119578701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54721687-A-G

http://identifiers.org/hco/8/GRCh38#119578733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54721719-C-A

119579030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54722010-G-A

119579112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54722083-C-G

119579213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54722360-T-A

119579280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54722427-C-T

119579535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54722648-C-T

119579612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54722743-C-T

119580003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54723114-A-G

119580015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54723126-T-A

119580019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54723130-A-G

119580069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54723393-C-T

119580078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54723402-G-T

119580273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54723599-C-T

119580288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54723615-A-G

119580307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54723634-G-A

119580307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54723634-G-T

119580308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54723635-G-A

119580308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54723635-G-T

119580412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54723736-A-G

119580483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54723804-G-A

119580483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54723804-G-C

http://identifiers.org/hco/8/GRCh38#119580663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54723992-C-A

119582038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725507-T-G

119582086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725572-C-G

119582164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725642-G-A

119582318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725793-A-G

119582318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725793-A-T

119582323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725798-T-C

119582344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725819-C-T

http://identifiers.org/hco/8/GRCh38#119582360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54725835-C-A

119582393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54725868-T-C

119582610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54726086-A-G

119582623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726098-G-A

119582623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726098-G-C

119582661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726136-T-C

119582668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726143-T-A

119582668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726143-T-G

119582688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726163-G-A

119582688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726163-G-C

119582688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726163-G-T

http://identifiers.org/hco/8/GRCh38#119582692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54726167-C-A

119582740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726211-G-T

119582828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726302-C-T

119583033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726455-A-G

119583033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54726455-A-T

119583595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727027-T-G

119583601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727033-G-T

119583651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727077-A-G

119583651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727077-A-T

119583692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727109-G-T

119583829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727245-A-G

119583891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727312-C-T

119584079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727497-G-T

119584086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727504-T-A

119584240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727655-A-G

119584268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727683-T-A

119584268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727683-T-C

119584289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727701-G-A

119584409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727737-T-G

119584567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54727834-A-G

http://identifiers.org/hco/8/GRCh38#119584660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54727925-A-C

119584766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728030-T-A

119585017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728250-C-T

119585098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728329-C-T

119585156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728392-G-A

119585156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728392-G-C

119585157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728393-G-A

119585188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728417-T-C

119585239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728458-G-A

119585334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728535-T-G

119585465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728628-G-C

119585572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728735-T-C

119585590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728755-C-T

119585616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728780-T-A

119585616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728780-T-C

119585619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728783-G-A

119585619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728783-G-C

http://identifiers.org/hco/8/GRCh38#119585750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54728905-A-C

119585769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54728921-C-T

119586122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54729249-A-G

119586138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54729265-G-A

119586167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54729291-T-C

119586177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54729299-A-G

119586230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54729352-A-G

119586343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54729465-A-G

119586527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54729651-G-A

119586650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54729761-G-C

119586846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54729947-A-G

119586963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54730057-G-A

119587004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54730109-G-A

119587004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54730109-G-T

119587092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54730174-G-T

http://identifiers.org/hco/8/GRCh38#119587217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54730274-A-C

119587218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54730275-T-C

119587218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54730275-T-G

http://identifiers.org/hco/8/GRCh38#119587250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54730307-A-C

119587335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54730389-C-T

119587404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54730457-A-T

119587722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54730791-G-T

119587874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54730925-G-T

119589100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54732167-T-C

119589118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54732184-A-G

119589118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54732184-A-T

119589194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54732254-T-C

119589432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54732506-C-T

119589687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54732743-T-C

119590038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733207-C-T

119590207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733364-T-C

119590388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733510-G-A

119590388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733510-G-T

119590426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733533-T-C

119590426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733533-T-G

http://identifiers.org/hco/8/GRCh38#119590447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54733554-C-A

119590447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733554-C-G

119590620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54733714-A-G

119590649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733743-A-G

119590683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733787-T-A

119590683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733787-T-C

http://identifiers.org/hco/8/GRCh38#119590693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54733803-A-C

119590699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733809-G-A

119590699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733809-G-C

119590699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733809-G-T

119590716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733834-T-A

119590716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733834-T-C

119590771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54733887-G-T

119590978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54734231-G-A

119590978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54734231-G-T

119591020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54734291-T-A

119591020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54734291-T-C

119591485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54734937-G-C

119591542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54735495-T-G

119591994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54736131-A-T

119592093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54736232-C-T

119592109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54736248-T-A

119592109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54736248-T-C

119592109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54736248-T-G

119592815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54736646-A-T

119592910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54736731-G-A

119592910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54736731-G-C

119592910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54736731-G-T

119593349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54738503-G-C

119593357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54738512-T-C

119593440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54738594-C-T

http://identifiers.org/hco/8/GRCh38#119593623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54738743-C-A

119593623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54738743-C-G

http://identifiers.org/hco/8/GRCh38#119593965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54739269-C-A

119593965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54739269-C-T

http://identifiers.org/hco/8/GRCh38#119593997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54739302-C-A

http://identifiers.org/hco/8/GRCh38#119594672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54739975-C-A

119594888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54740240-G-A

http://identifiers.org/hco/8/GRCh38#119594927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54740280-A-C

119594927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54740280-A-T

119595270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54740600-T-C

http://identifiers.org/hco/8/GRCh38#119595404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54740716-C-A

119595698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741025-A-G

119595707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741034-T-C

http://identifiers.org/hco/8/GRCh38#119595782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54741107-C-A

119595782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741107-C-T

119595790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741115-G-A

119595790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741115-G-T

119595976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 54741301-A-T

119596027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741352-G-T

119596083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741409-T-C

119596134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741465-T-C

119596144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741471-G-T

119596159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741486-G-A

119596165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741492-T-C

119596628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741906-C-G

119596790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54741969-A-G

119597101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54742258-G-C

119597276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54742432-C-T

119597655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54742819-C-T

119597844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54743027-A-G

http://identifiers.org/hco/8/GRCh38#119597991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54743181-C-A

119597991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54743181-C-T

119597992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54743182-G-A

119597992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54743182-G-T

119598038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54743221-T-G

119598808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54743968-G-T

119599299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54744455-T-C

http://identifiers.org/hco/8/GRCh38#119599446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54744552-C-A

119599483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54744597-A-G

119600398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745251-T-G

119600520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745372-A-G

119600532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745384-A-T

119600639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745487-G-A

119600639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745487-G-T

119600684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: synonymous variant
orthologous variants: 54745532-G-A

119600684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: synonymous variant
orthologous variants: 54745532-G-T

119600785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745631-A-G

119600829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745804-T-A

119600829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745804-T-C

119600883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745858-G-A

119600883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745858-G-C

119600883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745858-G-T

119600900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54745877-T-C

119601118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54746077-A-G

http://identifiers.org/hco/8/GRCh38#119601279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54746232-C-A

119601279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54746232-C-G

119601302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54746258-A-G

119601324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54746280-A-G

119601402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: synonymous variant
orthologous variants: 54746374-A-G

119601468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 54746440-G-A

119603127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54747120-A-T

119603334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54747327-T-C

119603769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54747963-G-A

119603777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54747971-G-A

119603837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54748029-C-G

119603845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54748038-T-G

http://identifiers.org/hco/8/GRCh38#119604340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54748216-A-C

http://identifiers.org/hco/8/GRCh38#119604560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54748426-C-A

119604611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54748521-T-A

119604611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54748521-T-G

119605936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54749187-T-C

119606400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54749650-A-T

119606483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54749712-A-T

119606589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54749820-C-T

119606646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54749870-C-T

119606719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54749944-T-G

119606848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54750100-G-A

119607297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54750543-A-G

119607352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54750599-C-T

119607649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54750716-T-G

119607691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54750729-G-A

119607691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54750729-G-T

http://identifiers.org/hco/8/GRCh38#119607775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54750800-C-A

119607775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54750800-C-T

119607884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54750911-G-T

119608163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54751186-C-G

119608265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54751283-G-A

http://identifiers.org/hco/8/GRCh38#119608414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54751429-A-C

119608629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54751714-G-A

http://identifiers.org/hco/8/GRCh38#119608650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54751756-C-A

119608711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54751900-G-A

119608766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54751954-T-C

http://identifiers.org/hco/8/GRCh38#119609269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54752431-C-A

119609269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54752431-C-T

119609449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54752571-T-C

119609829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54752949-T-C

119609971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54753090-G-A

119610429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54754176-A-G

119610439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54754186-A-G

119610443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54754190-T-G

119610640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54754509-C-T

119610641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54754510-G-A

119610669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54754532-G-A

119611020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54754852-T-C

119611035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54754867-C-G

119612365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54758201-G-C

119613122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54758597-T-C

119613158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54758631-C-G

119613217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54758692-C-T

119613280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54758756-C-T

119613641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54759096-G-A

119614700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54759620-G-C

119614725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54759645-T-C

119615099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54760031-A-T

119615731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54760612-T-C

119615745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54760626-C-T

119615753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54760634-T-C

119615999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54760861-C-T

119616083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54760954-T-C

119616184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54761023-C-T

119616624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54761429-T-G

119616985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54761755-C-T

119616986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54761756-C-T

119617042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54761795-G-A

http://identifiers.org/hco/8/GRCh38#119617077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54762203-C-A

119617077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762203-C-T

119617122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762254-A-G

119617263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762383-T-C

http://identifiers.org/hco/8/GRCh38#119617373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54762594-C-A

119617395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762615-G-A

119617449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762656-G-A

119617449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762656-G-C

119617449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762656-G-T

119617595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762801-C-T

119617643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762851-G-A

119617643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762851-G-T

http://identifiers.org/hco/8/GRCh38#119617674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54762880-C-A

119617674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54762880-C-T

119619124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764632-A-G

119619125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764633-G-A

119619125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764633-G-C

119619125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764633-G-T

http://identifiers.org/hco/8/GRCh38#119619200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54764700-C-A

119619204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764704-T-C

119619225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764725-A-G

119619236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 54764741-A-G

119619237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 54764742-C-T

119619247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 54764752-G-A

119619247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 54764752-G-T

119619258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 54764763-T-C

119619318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764824-T-A

119619318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764824-T-C

119619325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764831-A-G

119619325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764831-A-T

119619412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764919-T-A

119619412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764919-T-C

119619412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764919-T-G

http://identifiers.org/hco/8/GRCh38#119619435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54764938-C-A

119619435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54764938-C-T

119619553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54765050-G-A

119619663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54765166-G-A

119619689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54765192-G-A

119619718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54765221-A-G

119619747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54765250-T-A

119619826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54765326-G-A

119620373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54766763-C-G

119620796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54767698-A-G

119620814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54767716-C-T

119620843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54767744-C-T

119620844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54767745-C-T

119621287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54770125-C-T

http://identifiers.org/hco/8/GRCh38#119621376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54770207-A-C

119621376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54770207-A-T

119621432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 54770261-C-G

119621432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 54770261-C-T

http://identifiers.org/hco/8/GRCh38#119621532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54770361-C-A

http://identifiers.org/hco/8/GRCh38#119621563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54770392-C-A

119621563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54770392-C-G

119621563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54770392-C-T

119621575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54770404-G-A

119621575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54770404-G-T

http://identifiers.org/hco/8/GRCh38#119621624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54770454-C-A

119621639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54770469-T-C

119622356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771195-C-T

119622394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771227-G-C

119622576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771426-G-A

119622747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771569-A-G

119622747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771569-A-T

119622772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771611-T-C

119622775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771614-A-G

119623084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771874-G-A

119623122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771915-G-A

119623128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771921-T-G

119623158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54771948-G-A

http://identifiers.org/hco/8/GRCh38#119623171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54771961-A-C

119624831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54772143-G-A

119624936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54772243-A-G

119625011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54772321-C-T

119625172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54772465-A-G

119625345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54772634-T-G

119625683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54772916-T-C

119625839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54773070-C-T

119625850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54773081-T-A

http://identifiers.org/hco/8/GRCh38#119625858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54773089-C-A

119626767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54773636-T-A

119626767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54773636-T-C

http://identifiers.org/hco/8/GRCh38#119626832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54773702-C-A

119626881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54773751-T-G

119627063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54773924-C-T

119627073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54773934-T-C

119627080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54773941-C-T

119627562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54774085-T-G

http://identifiers.org/hco/8/GRCh38#119628000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54774516-A-C

119629196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54774862-A-G

119629286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54774945-C-T

119629375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54774993-A-G

119629419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54775017-G-A

119630073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54775591-G-A

119630441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54775729-A-G

119630453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54775741-C-T

119630508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54775804-A-G

http://identifiers.org/hco/8/GRCh38#119630561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54775854-C-A

119630579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54775871-T-C

119630754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54776020-C-T

119631634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54776361-A-G

119631884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54776523-A-G

119632162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54776892-A-G

http://identifiers.org/hco/8/GRCh38#119632235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54776957-C-A

119632287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54777010-G-A

119632287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54777010-G-T

119632474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54777306-C-G

119633098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54777632-A-G

http://identifiers.org/hco/8/GRCh38#119633212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54777755-A-C

119633355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54777908-C-G

119633357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54777910-A-G

119633373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54777927-C-G

119633374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54777928-T-G

119633446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54777994-T-C

119633446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54777994-T-G

119633513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54778057-G-A

119633513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54778057-G-T

119633566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54778109-C-T

119633575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54778282-A-G

119633621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54778330-T-A

119633784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54778471-C-T

http://identifiers.org/hco/8/GRCh38#119634251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54778654-A-C

119634499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54778886-A-G

http://identifiers.org/hco/8/GRCh38#119634547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54778944-C-A

119634863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54779762-A-G

119634955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54779855-C-G

119635123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54780023-C-T

119635142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54780042-A-G

119635245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54780118-A-G

119635495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54780373-T-C

119635689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54780544-C-G

119635941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54780790-A-T

119636108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54780938-T-C

119636187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54781047-T-A

119636743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54781596-C-T

119636948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54781811-T-C

119636986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54781834-A-G

119637074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54781899-T-A

119637179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54781983-T-C

119637182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54781986-G-C

119637300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54782105-C-T

http://identifiers.org/hco/8/GRCh38#119637336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54782142-A-C

http://identifiers.org/hco/8/GRCh38#119637413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54782220-C-A

119637528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54782311-T-G

119637724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54782505-G-A

119638500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 54783067-C-T

119638519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 54783086-G-C

119638519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 54783086-G-T

http://identifiers.org/hco/8/GRCh38#119638624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54783187-A-C

119638691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54783270-A-G

http://identifiers.org/hco/8/GRCh38#119638697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54783274-C-A

119638733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 54783310-C-T

119639524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54784104-T-A

119639559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54784139-A-G

http://identifiers.org/hco/8/GRCh38#119639567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54784147-C-A

119639607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54784179-G-A

119639827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54784357-G-A

119639827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54784357-G-T

http://identifiers.org/hco/8/GRCh38#119639832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54784362-C-A

119639861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54784387-G-C

119639976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54784497-C-T

119640088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54784612-A-T

119640221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54784741-G-A

119640695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54785256-A-G

http://identifiers.org/hco/8/GRCh38#119641274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54785824-C-A

119641348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54785890-G-A

119641575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, undefined
orthologous variants: 54786106-G-A

119641589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54786120-A-G

119642562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54786397-G-A

119642587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54786423-T-C

119642637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54786465-G-T

119642666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54786494-T-C

119643405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787144-T-C

119643555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787291-A-G

119643555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787291-A-T

119643603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787337-T-C

119643841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787564-A-G

119643841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787564-A-T

119643883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787596-T-C

119643884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787597-G-A

119643895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787608-T-C

119643977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787686-G-A

119643977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787686-G-C

119644020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787729-A-G

119644299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787983-C-T

119644300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54787984-G-A

http://identifiers.org/hco/8/GRCh38#119644335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54788017-A-C

119644873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54789221-T-C

119645058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54789880-A-G

119645119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54789903-T-A

119645180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54789964-A-G

119645213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54790007-T-C

119645847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54790297-G-T

119645853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54790303-C-T

http://identifiers.org/hco/8/GRCh38#119646333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54790465-C-A

119646849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54790955-C-G

119646882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54790987-A-G

119646882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54790987-A-T

119646953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54791044-C-G

119646953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54791044-C-T

119648144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54792424-G-A

119648209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54792484-A-G

119648750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54792983-C-T

119650723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54794322-A-G

119650754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54794328-T-C

119651129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54794566-C-G

119651129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54794566-C-T

119651139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54794576-T-C

119651252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54794678-G-A

119651524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54794878-A-G

119651581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54794934-A-G

119651628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54794979-T-A

119654788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54796484-A-G

119654788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54796484-A-T

119655338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, undefined
orthologous variants: 54797017-G-A

119655338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, undefined
orthologous variants: 54797017-G-T

119655383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, undefined
orthologous variants: 54797068-T-C

119655478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, undefined
orthologous variants: 54797163-G-A

119655634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54797316-C-T

119655644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54797326-C-T

119655675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54797357-G-A

119655714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54797396-T-C

119655874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54797557-G-C

119656098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54797781-C-T

http://identifiers.org/hco/8/GRCh38#119656165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54797835-A-C

119656165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54797835-A-T

119656204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54797874-A-T

http://identifiers.org/hco/8/GRCh38#119656310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54797985-A-C

119657238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54798522-T-C

http://identifiers.org/hco/8/GRCh38#119657288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54798569-C-A

119657462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54798726-A-G

119657841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54799119-T-C

119657948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54799222-C-T

119658561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54799986-G-A

119658632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54800042-C-T

119658806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54800200-C-T

119658809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54800203-G-A

119658861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54800255-G-A

119659501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54800898-C-T

http://identifiers.org/hco/8/GRCh38#119659530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54800927-C-A

119659672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54801620-C-T

119659842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54801762-G-A

119659842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54801762-G-T

119659952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54801876-T-G

119659962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54801890-A-T

119660109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54802026-C-T

119660205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54802182-C-T

119660413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54802394-G-A

119660581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54802554-C-G

119660581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54802554-C-T

119660586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54802559-G-A

119660646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54802629-T-C

119660650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54802633-C-T

119662832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54804633-C-T

119662837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54804638-C-G

119662837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54804638-C-T

119663481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54805262-G-A

119663481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54805262-G-T

119663737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54805516-C-T

119664992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54807047-G-A

119664992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54807047-G-C

119664992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54807047-G-T

119665314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54807395-A-G

119665520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54807598-T-A

119665572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54807647-C-T

119665848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54807926-A-G

119665857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54807935-A-G

119665922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54807998-A-G

119666059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54808296-G-A

119666131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54808363-A-T

119666328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54808770-A-T

119666361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54808803-T-A

http://identifiers.org/hco/8/GRCh38#119666461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54808898-C-A

119666461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54808898-C-T

119666496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54808929-A-G

119667799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54810265-A-T

119668164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54810620-G-T

119668200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54810654-C-T

http://identifiers.org/hco/8/GRCh38#119668261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54810697-A-C

119668265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54810701-G-A

119668265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54810701-G-T

119668376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54810795-T-A

119670064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54811697-T-A

119670360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54811955-T-C

119671332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54814203-T-A

119671357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54814221-C-T

119671657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54814471-G-T

119671772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54814577-G-A

119671772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54814577-G-T

119671857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron variant
orthologous variants: 54814655-A-T

119672129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54814912-G-A

119672496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54815180-G-C

http://identifiers.org/hco/8/GRCh38#119672923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54815590-C-A

119672923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54815590-C-G

119672923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54815590-C-T

119673110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54815791-G-A

119673175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54815858-T-C

119673315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54816007-A-G

119673357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54816049-G-A

119673357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54816049-G-C

119673357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54816049-G-T