190407932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52766710-C-T

190407972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, undefined
orthologous variants: 52766660-G-C

http://identifiers.org/hco/2/GRCh38#190408201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52766448-C-A

190408263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52766384-G-A

190408266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52766381-G-A

190408266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52766381-G-C

http://identifiers.org/hco/2/GRCh38#190408282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52766367-C-A

190408339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52766326-G-A

190408339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52766326-G-C

190408339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52766326-G-T

190408360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52766315-A-G

190408458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 52766214-G-T

190408600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 52766140-G-T

190408700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52766092-T-A

190408700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52766092-T-C

190408700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52766092-T-G

190409120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52765703-C-T

190409121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52765702-C-G

190409123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52765700-C-T

190409703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52765100-C-T

190409774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52765025-T-G

190409805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52764995-C-G

190409805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52764995-C-T

190409959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52764824-A-G

190410369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52764321-G-A

190410400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52764286-C-G

190410400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52764286-C-T

190410421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52764268-G-A

190410623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52764063-C-T

190411501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52764024-G-A

190411655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52763893-G-T

190411803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52763738-A-G

190412101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52763465-C-T

190412111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52763447-A-G

190412515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52763056-C-T

190412517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52763054-A-G

190412602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52762997-A-G

http://identifiers.org/hco/2/GRCh38#190412769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52762838-C-A

190412769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52762838-C-T

http://identifiers.org/hco/2/GRCh38#190412835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52762779-C-A

190412835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52762779-C-G

190412835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52762779-C-T

190412889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52762730-T-A

190413207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, undefined
orthologous variants: 52762402-T-C

190413307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52762296-A-G

190413354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52762249-G-A

190413706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52761904-T-C

190414463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52761566-A-G

190414483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52761539-A-G

190414687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52761332-C-T

190414729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52761284-G-A

190414942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52761074-C-T

190415060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52760977-C-T

190415538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52760832-G-A

190416396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52758640-A-G

190416539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52758513-G-T

190416542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52758510-A-T

190416609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52758445-G-C

190417272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52757592-G-A

190417419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52757243-G-A

190417512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52757153-A-T

190417663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52756985-G-A

190418793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52753811-C-T

190418923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52753705-G-C

190419292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52753355-G-A

http://identifiers.org/hco/2/GRCh38#190419345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52753299-C-A

190419684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52752956-G-A

190419977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52752700-G-A

190420312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52752497-C-T

190420326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52752483-C-G

190420523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52752285-C-T

http://identifiers.org/hco/2/GRCh38#190420568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52752241-C-A

190420599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52752221-T-G

190420694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52752109-G-T

http://identifiers.org/hco/2/GRCh38#190433355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52751273-C-A

190433355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52751273-C-T

190433402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52751229-A-G

190433481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52751170-G-A

190433565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52750502-C-T

190435214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52749712-G-A

190435214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52749712-G-T

190435899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52748974-A-G

190435910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52748963-G-A

190435910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52748963-G-C

190436001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52748888-T-A

190436001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52748888-T-G

190436005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 52748884-A-T

190436413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 52748475-T-C

190436575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant
orthologous variants: 52748313-T-A

190436628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant
orthologous variants: 52748260-A-G

http://identifiers.org/hco/2/GRCh38#190437059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52747823-A-C

190437059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant
orthologous variants: 52747823-A-G

190437134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, stop_gained
orthologous variants: 52747748-C-T

190437179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant
orthologous variants: 52747703-A-G

190437410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant
orthologous variants: 52747472-T-C

190437569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 52747313-C-G

190437569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 52747313-C-T

http://identifiers.org/hco/2/GRCh38#190437594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52747287-C-A

190437594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52747287-C-T

190437595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52747286-A-G

190437688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52747221-G-T

190437975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52746947-C-T

190438094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52746730-G-A

190438719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52746450-C-T

190438810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52746352-C-T

190438928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52746240-T-C

190439069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52746107-T-C

190439099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52746074-C-T

190439298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52745899-G-A

190439298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52745899-G-T

190439410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52745757-G-A

190439422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52745745-G-A

190439560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52745661-T-C

190440404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52743842-C-T

190440807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52743434-T-C

190441287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52743024-T-C

190441342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742969-A-G

190441342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742969-A-T

190441358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742956-G-T

190441488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742871-G-A

190441488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742871-G-T

190441772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742630-C-T

190441805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742614-A-G

190441989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742445-G-A

190442103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742067-G-C

190442103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742067-G-T

190442107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52742063-G-T

190442485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52741629-T-A

190442485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52741629-T-G

190442496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: 52741620-G-A

http://identifiers.org/hco/2/GRCh38#190442563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52741555-C-A

190442665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52741458-A-G

190442680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52741452-T-C

190442734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52741394-G-T

190442803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52741324-T-G

190442812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52741315-T-A

190442834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52741312-G-A

190442836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52741310-C-G

190442836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52741310-C-T

190442982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52741182-T-C

http://identifiers.org/hco/2/GRCh38#190443119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52741050-C-A

190443141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52741028-G-A

190443141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52741028-G-T

190443274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52740927-G-T

190443300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52740901-C-T

190443304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52740897-A-T

190443364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52740836-G-A

http://identifiers.org/hco/2/GRCh38#190443496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52740722-C-A

190444079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52740194-G-A

190444101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52740171-T-C

http://identifiers.org/hco/2/GRCh38#190444185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52740117-A-C

190444212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52740095-T-C

190444239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52740076-G-C

190444471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52739926-A-G

190444720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52739694-A-G

190445814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52731611-G-A

190445963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52731490-C-T

190446286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52731215-A-G

190446900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52730454-G-A

190447098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52730243-A-T

190447496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52729906-G-A

190447496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52729906-G-C

190447911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52729069-G-A

190448067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52728928-T-G

190448128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52728867-G-A

190448214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52728791-T-C

190448449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52728603-T-C

190448449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52728603-T-G

190448647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52728423-T-C

190448938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52728146-G-A

190449162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52727948-G-A

190450455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52727418-G-T

190450471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52727402-T-C

190450935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52727296-C-T

190450977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52727271-T-C

http://identifiers.org/hco/2/GRCh38#190450982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52727266-A-C

190451081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52727168-C-T

190451111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52727138-C-T

190451263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52727112-C-T

190451276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52727098-G-C

190451304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52727070-A-G

190451526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52726852-C-T

190451583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52726798-C-T

190451673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52726611-G-A

190451853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52726439-G-A

190451855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52726437-G-A

190452393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52725721-G-A

190452398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52725719-G-A

190452398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52725719-G-C

http://identifiers.org/hco/2/GRCh38#190454551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52725076-C-A

190454551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52725076-C-T

190454609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52725015-G-T

http://identifiers.org/hco/2/GRCh38#190454622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52725002-C-A

190455000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52724687-A-T

190455027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52724676-T-C

190456675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52724038-A-G

190456762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52723963-C-T

http://identifiers.org/hco/2/GRCh38#190457003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52723737-C-A

190457003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52723737-C-T

190457078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52723674-C-T

190457094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52723658-A-G

190457277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52723571-C-G

190457656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52723228-T-A

190457845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52722973-A-G

190459403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52721828-A-G

190459466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52721769-A-G

190459880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52721403-C-T

http://identifiers.org/hco/2/GRCh38#190460337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52720955-C-A

http://identifiers.org/hco/2/GRCh38#190460362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#52720930-C-A

190460530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52720758-G-A

190460666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52720628-A-G

190460826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52720479-G-A

190464846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719898-G-A

190464846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719898-G-T

190465028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719756-T-C

190465038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719746-T-C

http://identifiers.org/hco/2/GRCh38#190465075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52719710-C-A

190465077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719708-A-G

190465081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719704-A-G

190465091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719693-G-T

190465387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719446-T-C

190465539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719355-T-C

190465539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719355-T-G

190465674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719234-T-G

190465679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719229-C-T

190466052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719137-G-C

190466115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52719092-T-G

190466679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52718098-A-G

190466839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52717951-C-G

190466839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52717951-C-T

190466852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52717938-T-C

190467004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52717787-A-G

190467090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52717726-C-T

190467170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52717654-G-T

190467192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52717641-C-G

190467722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52717383-T-C

http://identifiers.org/hco/2/GRCh38#190467761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52717344-A-C

190468362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52716826-A-G

http://identifiers.org/hco/2/GRCh38#190468378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52716810-A-C

190468657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52716550-C-T

190468661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52716546-G-T

190468685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52716532-T-C

190469078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52716366-T-C

http://identifiers.org/hco/2/GRCh38#190469141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52716320-C-A

190469175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52716284-G-A

http://identifiers.org/hco/2/GRCh38#190469383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#52716081-C-A

190469383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 52716081-C-T

http://identifiers.org/hco/2/GRCh38#190469406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#52716058-A-C

http://identifiers.org/hco/2/GRCh38#190469558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#52715899-C-A

190469671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715789-T-G

http://identifiers.org/hco/2/GRCh38#190469703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52715770-A-C

190469703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715770-A-G

190469703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715770-A-T

190469716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715757-T-A

190469716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715757-T-C

190469716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715757-T-G

190469737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715753-T-C

190469887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715603-T-C

http://identifiers.org/hco/2/GRCh38#190469915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52715568-C-A

190469915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715568-C-T

190469929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715556-G-A

190469929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715556-G-T

190469952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715529-G-A

190469952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715529-G-T

190470157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715377-G-T

190470199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715312-T-A

190470266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715296-C-G

190470498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52715072-T-A

190470587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52714968-G-A

190470793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52714818-A-G

http://identifiers.org/hco/2/GRCh38#190470845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52714764-A-C

190471005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52714596-G-T

190477072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713986-G-A

190477111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713948-G-A

190477247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713833-T-C

190477273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713815-C-G

190477312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713776-T-A

190477396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713692-G-T

http://identifiers.org/hco/2/GRCh38#190477531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52713392-C-A

190477561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713362-T-C

190477773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713215-G-A

190477924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713084-A-G

http://identifiers.org/hco/2/GRCh38#190477940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52713070-C-A

190477956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713054-G-A

190477957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52713053-C-G

190478606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52712474-T-C

190478909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52712054-G-A

190478909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52712054-G-C

http://identifiers.org/hco/2/GRCh38#190479095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52711964-C-A

190479358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52711803-T-C

190479436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52711736-G-A

190479440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52711732-T-C

190479460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52711711-C-T

190479614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52711601-A-T

190479633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52711582-G-A

190479836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52710856-G-A

190479859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52710834-G-T

190480324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52710238-A-T

190480363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52710222-C-T

190480374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52710211-T-C

190480384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52710201-T-A

190480614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52710015-C-T

190480784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52709886-A-G

190481384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52709131-T-G

190481510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52709014-A-G

190481638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52708885-T-C

190481695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52708838-C-G

190481854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52708700-T-C

190481878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52708636-A-G

190481907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52708610-C-T

190482176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52708401-C-G

http://identifiers.org/hco/2/GRCh38#190482376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52708169-A-C

190482434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52708112-A-T

190482448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52708098-C-T

190482630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52707919-C-T

190482736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52707559-A-G

http://identifiers.org/hco/2/GRCh38#190482758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52707537-A-C

http://identifiers.org/hco/2/GRCh38#190482863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52707453-A-C

190482863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52707453-A-T

190482874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52707442-T-C

190483075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52707110-G-A

190483136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52707027-C-T

190483182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52706958-G-A

http://identifiers.org/hco/2/GRCh38#190483185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52706955-C-A

190483197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52706943-T-A

http://identifiers.org/hco/2/GRCh38#190483360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52706797-A-C

190484005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52706525-C-T

190484044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52706485-G-T

190484051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52706481-A-G

190485103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52705938-T-C

190485141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52705901-T-A

190485466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52705532-T-C

190485905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52705008-T-C

190485967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52704946-A-G

190486085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52704848-T-G

190488524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702847-G-A

190488524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702847-G-T

190488621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702640-A-G

190488629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702629-A-G

190488710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 52702550-G-A

190488740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 52702520-G-A

190488842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702420-T-C

190488863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702402-A-G

190488863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702402-A-T

190488866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702399-A-G

http://identifiers.org/hco/2/GRCh38#190488886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52702386-A-C

190488886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702386-A-G

190488963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702339-T-A

190488963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52702339-T-C

190489474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701860-G-A

190489659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701739-G-T

190489933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701421-G-A

190489933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701421-G-C

190489933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701421-G-T

http://identifiers.org/hco/2/GRCh38#190490004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52701357-A-C

190490004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701357-A-G

190490115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701265-A-G

190490162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701218-T-C

190490296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701049-G-C

http://identifiers.org/hco/2/GRCh38#190490299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52701046-C-A

190490299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701046-C-G

190490299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52701046-C-T

190497391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52700290-T-C

190497483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52700200-G-A

190497483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52700200-G-C

190497538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52700145-G-A

190497538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 52700145-G-C

190497585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52700098-C-G

190497864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52699854-T-A

190497864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52699854-T-C

http://identifiers.org/hco/2/GRCh38#190497931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52699794-C-A

190497931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52699794-C-T

190498028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52699695-T-A

190498034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52699689-T-C

190498094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52699625-T-C

190498113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52699602-G-A

190498144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52699572-A-G

190498309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52699418-A-G

190498311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52699416-C-T

http://identifiers.org/hco/2/GRCh38#190498617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52698683-C-A

190498770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52698571-T-C

190499424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52698272-T-C

190499446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52698253-G-T

190499638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52698082-C-G

190499703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52698020-G-T

190499726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697998-A-G

190499791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697921-G-A

190499791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697921-G-C

190499791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697921-G-T

190499865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697848-T-A

190499865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697848-T-C

190499884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697830-T-C

190500204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 52697513-G-A

190500220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697497-G-A

http://identifiers.org/hco/2/GRCh38#190500365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52697359-A-C

190500365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697359-A-G

http://identifiers.org/hco/2/GRCh38#190500371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52697353-A-C

190500371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697353-A-G

190500384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697252-T-C

190500384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697252-T-G

http://identifiers.org/hco/2/GRCh38#190500524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52697143-A-C

190500524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697143-A-G

http://identifiers.org/hco/2/GRCh38#190500527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52697140-C-A

190500527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697140-C-T

190500529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697138-G-A

190500529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697138-G-C

190500529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697138-G-T

190500622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52697046-C-G

190500960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52696741-G-A

190500960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52696741-G-T

http://identifiers.org/hco/2/GRCh38#190501111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52696597-A-C

190501271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52696449-G-T

190501275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52696445-G-T

190501333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52696394-A-G

190501408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52696313-A-G

190501557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52696174-G-A

190501557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52696174-G-T

http://identifiers.org/hco/2/GRCh38#190501905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52695870-A-C

190501905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52695870-A-G

190501975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52695806-T-G

190502013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52695768-G-A

190502030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52695751-G-A

190506087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691956-G-T

http://identifiers.org/hco/2/GRCh38#190506132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52691926-C-A

190506426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691648-T-A

http://identifiers.org/hco/2/GRCh38#190506592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52691497-C-A

190506592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691497-C-T

190506688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691403-T-C

190506731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691351-T-C

190506853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691232-C-T

190507003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691159-A-G

190507044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691139-T-C

190507056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691127-G-C

190507056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691127-G-T

http://identifiers.org/hco/2/GRCh38#190507116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52691081-C-A

190507152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52691046-A-G

http://identifiers.org/hco/2/GRCh38#190507228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52690972-C-A

190507412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52690838-C-T

190507463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52690786-A-G

190507466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52690783-G-A

190507476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52690773-C-T

http://identifiers.org/hco/2/GRCh38#190507525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52690718-A-C

190507663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52690404-A-G

190507811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52690277-C-G

190507905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52690177-A-G

190508365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52689695-G-T

190508393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52689666-T-A

http://identifiers.org/hco/2/GRCh38#190508394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52689665-C-A

http://identifiers.org/hco/2/GRCh38#190508446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52689624-C-A

http://identifiers.org/hco/2/GRCh38#190508461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52689609-C-A

190508733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52689366-T-C

190508738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52689361-T-A

http://identifiers.org/hco/2/GRCh38#190509036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52689109-A-C

190509036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52689109-A-G

190509039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52689106-G-A

190509039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52689106-G-T

http://identifiers.org/hco/2/GRCh38#190509109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52689062-C-A

190509109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52689062-C-T

190509146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 52689025-C-T

http://identifiers.org/hco/2/GRCh38#190509171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24711
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52689000-C-A