115962484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983127-A-G

115962484-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983127-A-T

115962485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983128-G-A

115962485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983128-G-C

115962518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983158-G-A

115962518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983158-G-T

115962552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983197-G-C

115962552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983197-G-T

http://identifiers.org/hco/5/GRCh38#115962555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46983200-C-A

115962555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983200-C-T

115962557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983202-G-A

115962557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983202-G-T

http://identifiers.org/hco/5/GRCh38#115962586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46983236-C-A

115962586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983236-C-G

115962602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983243-G-T

http://identifiers.org/hco/5/GRCh38#115962606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46983247-C-A

115962606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 46983247-C-T

115962657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983298-G-A

115962657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983298-G-C

115962657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983298-G-T

http://identifiers.org/hco/5/GRCh38#115962688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#46983329-C-A

115962688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 46983329-C-T

115962692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 46983333-C-G

http://identifiers.org/hco/5/GRCh38#115962737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/18/GRCm39#46983378-C-A

115962737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983378-C-G

115962783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983424-G-A

115962783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983424-G-T

115962839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 46983471-T-G

http://identifiers.org/hco/5/GRCh38#115962879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46983508-C-A

115962879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983508-C-G

115962879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 46983508-C-T

115962880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983509-G-A

115962880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983509-G-C

115962880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983509-G-T

115963108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 46983740-C-T

http://identifiers.org/hco/5/GRCh38#115963151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#46983783-C-A

115963151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 46983783-C-T

115964256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46984880-C-G

115964422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46985038-C-T

115964948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46985667-A-G

115964979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46985697-C-G

115964979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46985697-C-T

115965085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46985790-T-A

115965085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46985790-T-C

115968921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46987956-G-A

115968957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46987991-G-A

115968966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46988000-A-G

115978425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993002-G-T

115978504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993070-T-C

115978541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993109-A-G

115978698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993249-G-C

115978705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993255-G-A

115979088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993642-G-T

115979164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993716-C-G

115979164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993716-C-T

115979192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993744-C-T

http://identifiers.org/hco/5/GRCh38#115979247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46993813-C-A

115979247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993813-C-G

115979315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46993999-G-A

http://identifiers.org/hco/5/GRCh38#115979413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46994187-C-A

115979413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46994187-C-T

115979420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46994194-A-G

115979453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46994220-A-G

115979453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46994220-A-T

115979770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46994532-G-A

115979850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46994619-T-A

115980063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46994809-G-T

115980302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46995040-G-T

115980474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46995209-C-T

http://identifiers.org/hco/5/GRCh38#115980562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46995290-A-C

115980639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46995341-C-T

115981054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46995819-G-A

115981070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46995844-C-T

115981870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46996442-T-C

115982203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46996727-G-T

115982214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46996752-G-A

115982229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46996781-T-C

115982452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997002-C-T

http://identifiers.org/hco/5/GRCh38#115982577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46997100-A-C

115983090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997564-T-C

115983131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997605-G-A

115983138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997612-G-C

115983138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997612-G-T

115983158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997632-A-G

115983159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997633-G-T

115983173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997647-A-G

115983217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997658-C-G

115983231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997672-T-G

115983299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 46997752-G-A

115983299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 46997752-G-C

115983299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 46997752-G-T

115983429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 46997882-G-A

115983461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997906-T-C

115983573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46997987-T-C

115983601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46998014-G-C

115983739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46998151-G-C

115983897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46998309-C-T

115983962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46998349-A-G

http://identifiers.org/hco/5/GRCh38#115984364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46998674-A-C

115984501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46999399-G-C

115984768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46999663-A-G

115984785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46999674-T-C

115984785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46999674-T-G

115984826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46999708-C-G

115984849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46999724-T-C

115984939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46999978-T-C

115985733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47000305-G-C

115985745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47000317-A-G

115985786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47000344-C-T

http://identifiers.org/hco/5/GRCh38#115985914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47000492-C-A

115985980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47000553-G-A

115985980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47000553-G-T

115985991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47000564-C-G

http://identifiers.org/hco/5/GRCh38#115986016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47000589-A-C

115986373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47000890-G-A

115986373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47000890-G-T

115986431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47000941-A-T

http://identifiers.org/hco/5/GRCh38#115986542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47001049-A-C

115986644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47001150-A-T

115986742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47001225-G-A

115986803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47003117-G-A

115986803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47003117-G-C

115987210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47003397-T-C

115987736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47006775-G-C

http://identifiers.org/hco/5/GRCh38#115987756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47006795-C-A

115987847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 47006883-A-G

http://identifiers.org/hco/5/GRCh38#115988001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47007035-C-A

115988001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47007035-C-T

http://identifiers.org/hco/5/GRCh38#115988020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47007054-A-C

115988020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47007054-A-G

http://identifiers.org/hco/5/GRCh38#115988022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47007056-C-A

http://identifiers.org/hco/5/GRCh38#115988042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47007075-C-A

115988078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47007120-A-G

115988078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47007120-A-T

115988176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47007211-G-A

115988184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47007219-T-A

115988276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47007302-G-A

115988323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47007349-C-G

115988504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47007519-A-G

115988707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47007709-C-G

115991977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47009793-A-G

115991977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47009793-A-T

115992000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47009820-G-A

115992000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47009820-G-C

115992000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47009820-G-T

115992187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47010014-T-C

115992380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010203-T-G

115992381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010204-T-A

115992381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010204-T-C

115992382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010205-A-G

115992384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010207-A-T

115992397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010224-T-A

115992767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010399-G-A

http://identifiers.org/hco/5/GRCh38#115992823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47010444-A-C

115993016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010629-A-T

115993148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010752-T-C

http://identifiers.org/hco/5/GRCh38#115993218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47010807-A-C

115993218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010807-A-G

115993218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47010807-A-T

115993590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47011154-T-C

115993590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47011154-T-G

115993625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47011189-G-A

115993625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47011189-G-T

115993657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47011218-A-T

115993672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47011233-G-A

115993672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47011233-G-T

115993724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47011278-C-T

115993930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47011480-T-C

115998920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47012860-A-T

115998942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47012882-G-A

115998942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47012882-G-T

115999217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47013152-A-G

115999217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47013152-A-T

115999243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47013178-T-G

115999729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47013652-G-C

115999797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 47013720-C-G

115999797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 47013720-C-T

116000054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47013970-T-A

116000068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47013984-C-T

116000369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47014262-T-C

http://identifiers.org/hco/5/GRCh38#116000380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47014273-A-C

116000380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47014273-A-G

116000426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 47014318-G-C

116000474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 47014366-G-A

116000474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 47014366-G-C

116000474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 47014366-G-T

116000529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47014418-G-A

116000563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47014451-A-T

116000743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47014635-G-A

116000756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47014648-A-G

116000784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47014678-T-C

116000784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47014678-T-G

http://identifiers.org/hco/5/GRCh38#116000808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47014701-C-A

116000808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47014701-C-T

http://identifiers.org/hco/5/GRCh38#116000946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47015149-C-A

116000964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015166-T-C

116000967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015169-G-A

116000967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015169-G-C

116000968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015170-T-C

http://identifiers.org/hco/5/GRCh38#116001008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47015211-C-A

116001054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015258-T-G

116001089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 47015293-T-C

116001112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 47015316-A-G

116001178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 47015382-G-A

116001178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 47015382-G-C

http://identifiers.org/hco/5/GRCh38#116001270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47015472-C-A

116001270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015472-C-T

116001278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015480-G-A

116001278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015480-G-C

http://identifiers.org/hco/5/GRCh38#116001328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47015529-C-A

116001328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015529-C-T

116001388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015583-T-C

116001476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015660-G-A

116001848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47015937-A-G

116001925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47016006-C-T

116002397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017050-G-T

http://identifiers.org/hco/5/GRCh38#116002453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47017108-A-C

116002552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017205-C-T

116002591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017248-C-T

116002706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017363-T-A

116002706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017363-T-C

116002707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017364-G-T

http://identifiers.org/hco/5/GRCh38#116002727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47017384-C-A

116002727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017384-C-G

116002772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017425-T-A

116002772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017425-T-C

116002939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017635-T-C

116002972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017679-A-G

116002983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017721-T-A

116002983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017721-T-C

116002992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017730-T-A

116002992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017730-T-C

116002993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017731-G-A

116002993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017731-G-T

116003020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017848-T-C

116003020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017848-T-G

116003029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017859-T-C

116003070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017911-C-G

116003070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017911-C-T

116003149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017985-G-T

116003156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017992-G-A

116003156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47017992-G-T

116003206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018051-G-T

http://identifiers.org/hco/5/GRCh38#116003357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47018202-C-A

116003357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 47018202-C-T

116003374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 47018219-T-C

116003444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018277-A-G

116003454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018287-T-G

116003459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018292-T-C

116003459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018292-T-G

116003473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018301-A-G

116003474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018302-C-T

116004137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018603-T-G

116004180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018645-G-A

116004180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018645-G-C

116004236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018708-C-G

http://identifiers.org/hco/5/GRCh38#116004246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47018718-C-A

116004502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018903-G-A

116004558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47018976-T-C

116005297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47019586-C-T

116005388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47019681-C-T

116005403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47019696-A-G

116005403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47019696-A-T

116005496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47019788-G-A

116005602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47019894-G-C

116005805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47020091-G-T

116005808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47020094-G-A

116005808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47020094-G-T

116005823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47020110-G-A

116005823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47020110-G-T

116005846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47020132-A-G

116005846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47020132-A-T

116005898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 47020169-G-A

116005976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47020247-A-G

http://identifiers.org/hco/5/GRCh38#116006005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47020276-C-A

116006028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47020299-T-A

116006028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47020299-T-C

116006087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47020358-A-G

116006131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47020511-G-A

116006158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47020538-T-C

116006220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47020598-C-T

116006463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47020866-A-G

116006778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47021115-C-T

116006816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47021152-A-G

116006900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47021229-C-T

116007136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47021544-T-C

116007207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47021612-A-G

116007580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47021997-C-G

http://identifiers.org/hco/5/GRCh38#116010503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47022209-A-C

116010753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 47022465-T-C

116010759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 47022471-T-C

116010764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 47022476-C-T

116010765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 47022477-A-G

116010804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 47022516-A-G

116010804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 47022516-A-T

116010981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47022693-T-C

116011155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47022859-C-G

116011296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47023021-A-G

116011682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47023436-G-A

116011682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47023436-G-T

116011803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47023521-A-G

http://identifiers.org/hco/5/GRCh38#116011870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47023590-A-C

116011870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47023590-A-G

116011870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47023590-A-T

116012322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47023845-A-T

116012487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47024008-G-A

116012487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47024008-G-T

http://identifiers.org/hco/5/GRCh38#116012516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47024035-A-C

116012532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47024058-T-A

116012532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47024058-T-C

116012534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47024060-A-T

116012556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47024097-G-A

116012753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47024267-A-G

116012768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47024284-G-T

116012867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47025117-C-T

http://identifiers.org/hco/5/GRCh38#116013135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47025338-C-A

116013135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47025338-C-G

116013249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47025449-T-C

116013335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47025621-G-T

116013373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47025716-G-T

116013515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47025856-C-T

116013641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47025975-T-A

116013733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47026069-T-G

116013910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47026237-A-G

116013966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47026302-T-C

116014100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47026420-A-G

116014168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47026488-T-C

116014227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47026547-G-C

116014341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47026659-G-A

116014341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47026659-G-T

116014378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47026698-G-A

116014378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47026698-G-T

116014500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47026820-C-G

116014500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47026820-C-T

116014580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47026899-A-G

116014609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47026927-A-T

116014668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47026987-T-A

116014668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47026987-T-G

http://identifiers.org/hco/5/GRCh38#116015130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47027504-C-A

116015186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47027558-T-C

116015227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47027606-T-C

116015273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47027652-T-C

116015273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47027652-T-G

116015291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47027670-C-T

116015380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47027768-A-T

116015432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47027819-A-G

116015432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47027819-A-T

116015443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47027830-A-G

116015443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47027830-A-T

116015449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47027836-T-A

116015449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47027836-T-G

http://identifiers.org/hco/5/GRCh38#116015513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47027886-C-A

116015513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47027886-C-T

116015590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47027941-A-G

116015652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47028006-A-G

116015773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47028127-G-A

116015782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47028136-G-T

http://identifiers.org/hco/5/GRCh38#116015784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47028138-C-A

116015784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47028138-C-T

116015845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47028570-G-A

116015859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47028584-T-A

http://identifiers.org/hco/5/GRCh38#116015924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47028648-A-C

http://identifiers.org/hco/5/GRCh38#116015929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47028653-A-C

116016101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47031984-A-G

116016343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47032207-T-C

116016892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47032535-G-A

116021776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47032930-A-G

116021990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47033057-T-C

116022115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47033192-T-C

116022175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47033319-T-C

116022179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47033323-T-C

116022183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47033327-T-A

116022188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47033333-C-G

116022269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47033433-A-G

116022332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47033496-A-G

http://identifiers.org/hco/5/GRCh38#116022383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47033542-C-A

116025687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47037977-T-A

116025689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47037979-C-T

116025699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47037989-A-G

116025947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47038254-G-A

116025950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47038257-C-G

116026007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47038312-G-A

116026054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47038359-A-G

116026122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038427-G-A

116026144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038490-C-G

116026144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038490-C-T

http://identifiers.org/hco/5/GRCh38#116026252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47038597-C-A

116026252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038597-C-T

116026273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038616-G-A

116026273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038616-G-C

116026273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038616-G-T

116026343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038668-T-C

116026411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038756-G-T

116026440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038787-G-A

116026440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038787-G-T

116026544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038882-A-G

116026571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038906-A-G

116026571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038906-A-T

116026596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038934-G-T

116026599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038937-T-G

116026611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47038949-G-T

http://identifiers.org/hco/5/GRCh38#116026700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47039070-A-C

http://identifiers.org/hco/5/GRCh38#116026743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47039112-C-A

116026743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47039112-C-T

116026785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47039152-G-A

116026785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47039152-G-T

http://identifiers.org/hco/5/GRCh38#116026845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47039198-C-A

116026881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47039264-G-T

116026910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47039293-C-T

http://identifiers.org/hco/5/GRCh38#116027001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47039366-A-C

116027001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47039366-A-G

116027169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47039504-A-G

116027296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26904
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47039647-A-G