http://identifiers.org/hco/10/GRCh38#101570704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45533874-A-C

101570704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: non coding transcript exon variant
orthologous variants: 45533874-A-G

101570915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45534081-G-A

101571568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45534655-A-G

101571609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45534679-C-G

101571609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45534679-C-T

101572002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45535007-T-C

101572081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45535071-G-A

101572081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45535071-G-C

101572457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45535483-C-T

101572545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45535550-T-C

101572639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45535647-A-T

http://identifiers.org/hco/10/GRCh38#101572685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45535694-C-A

101572933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45535907-G-A

101573873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45537286-G-A

http://identifiers.org/hco/10/GRCh38#101574868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45538181-C-A

101574991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45538287-G-A

101575033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45538330-G-A

101575033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45538330-G-C

101575103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45538408-C-T

101575272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45538631-A-G

101575740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45538947-C-G

101575752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45538959-C-T

101575759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45538966-C-T

101578457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45540388-T-C

101578686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45540566-G-A

101578748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45540595-G-A

101578753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45540600-A-G

101578760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45540607-T-C

http://identifiers.org/hco/10/GRCh38#101578774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45540616-C-A

101578796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45540641-C-T

101578864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45540695-G-T

101578881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45540714-G-T

101578926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45540759-C-T

101578938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45540768-A-T

101579045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45540866-T-C

101579045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45540866-T-G

101579076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45540895-G-A

101579076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45540895-G-C

101579076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45540895-G-T

101579121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45540937-G-A

101579121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45540937-G-T

101579219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45541041-G-A

101579219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45541041-G-T

101579305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45541111-C-T

101579307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45541114-T-C

101579353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45541159-G-A

101579353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45541159-G-T

101579409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45541204-G-T

101579440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45541232-C-T

101579569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45541361-G-A

101579573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45541365-C-T

101579660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45541452-G-A

101579887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45541685-C-T

http://identifiers.org/hco/10/GRCh38#101579902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45541704-C-A

101579919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45541721-A-G

http://identifiers.org/hco/10/GRCh38#101579938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45541740-C-A

101580018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45541791-G-A

101580018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45541791-G-T

http://identifiers.org/hco/10/GRCh38#101580024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45541795-C-A

101580330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542030-A-T

101580520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542190-G-A

101580520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542190-G-T

101580563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542224-G-A

101580563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542224-G-T

101580567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542228-A-G

101580711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542301-A-G

101580712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542302-G-A

101580712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542302-G-C

101580712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542302-G-T

101580738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542330-G-A

101580738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542330-G-C

http://identifiers.org/hco/10/GRCh38#101580754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45542346-C-A

101580754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542346-C-T

101580858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542417-A-G

101580877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542436-G-A

101580877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542436-G-T

101580878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542437-A-G

101580878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542437-A-T

101581007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542537-C-G

http://identifiers.org/hco/10/GRCh38#101581014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45542543-C-A

101581021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542550-G-T

101581046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542563-C-T

101581047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542564-T-C

101581136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542594-T-A

101581136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542594-T-C

101581136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542594-T-G

101581140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542598-G-A

101581140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542598-G-T

http://identifiers.org/hco/10/GRCh38#101581142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45542600-C-A

http://identifiers.org/hco/10/GRCh38#101581246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45542716-A-C

101581246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542716-A-G

http://identifiers.org/hco/10/GRCh38#101581275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45542745-C-A

101581323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542786-C-T

101581327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542792-T-G

101581381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542853-C-T

101581384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542856-G-A

http://identifiers.org/hco/10/GRCh38#101581390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45542862-C-A

http://identifiers.org/hco/10/GRCh38#101581412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45542884-C-A

101581478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45542934-T-C

101581610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45543058-A-G

101581620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45543067-G-T

http://identifiers.org/hco/10/GRCh38#101581654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45543095-A-C

101581657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45543098-G-T

101581675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45543116-T-G

http://identifiers.org/hco/10/GRCh38#101582611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45543430-C-A

101582632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45543444-T-A

101582632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45543444-T-C

101582644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45543456-G-A

101582644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45543456-G-T

101582729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45543517-T-C

101582764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45543531-G-A

101582864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45543631-T-G

101582945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45543712-G-T

101582948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45543723-T-A

101582948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45543723-T-C

http://identifiers.org/hco/10/GRCh38#101583202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45543900-C-A

101583202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45543900-C-G

101583218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45543916-G-A

101583384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45544224-C-G

http://identifiers.org/hco/10/GRCh38#101583407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45544247-C-A

101583422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45544272-G-C

101583422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45544272-G-T

101583472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45544326-A-G

101583535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45544388-G-C

101584597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45546149-G-A

101584597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45546149-G-T

101584598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45546150-G-A

101584598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45546150-G-T

101584733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45546285-G-A

101584808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45546360-G-A

101584833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45546385-G-A

101584833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45546385-G-T

101584851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45546403-G-A

101584855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45546407-G-A

101584855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45546407-G-T

101585012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546509-G-A

101585012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546509-G-T

101585014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546511-G-T

101585018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546515-T-C

101585031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546528-A-G

101585031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546528-A-T

http://identifiers.org/hco/10/GRCh38#101585273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45546670-C-A

101585273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546670-C-T

101585305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546684-A-G

101585347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45546726-T-C

101585374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45546753-G-A

101585390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45546769-A-G

101585414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45546793-C-T

101585515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546895-G-C

101585515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546895-G-T

http://identifiers.org/hco/10/GRCh38#101585517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45546897-C-A

101585517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546897-C-T

http://identifiers.org/hco/10/GRCh38#101585519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45546899-C-A

101585519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546899-C-T

http://identifiers.org/hco/10/GRCh38#101585529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45546908-C-A

101585584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546974-A-G

http://identifiers.org/hco/10/GRCh38#101585590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45546982-C-A

101585590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546982-C-T

101585793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546998-T-A

101585793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45546998-T-G

101585799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45547004-T-C

101586045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45547247-T-C

101587202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 45547984-T-A

101587202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 45547984-T-C

101587458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 45548200-G-T

http://identifiers.org/hco/10/GRCh38#101587494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45548220-C-A

101587494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548220-C-G

http://identifiers.org/hco/10/GRCh38#101587495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45548221-C-A

101587495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548221-C-G

101587495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548221-C-T

101587498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548224-G-C

101587498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548224-G-T

101587530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548240-T-C

101587530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548240-T-G

http://identifiers.org/hco/10/GRCh38#101587577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45548292-C-A

101587593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548309-G-C

101587593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548309-G-T

101587608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548324-T-C

101587670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548389-G-A

101587670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548389-G-T

101587676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548395-T-A

101587676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548395-T-C

101587683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548402-A-G

101587686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548405-G-A

101587686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548405-G-T

http://identifiers.org/hco/10/GRCh38#101587690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45548409-C-A

101587690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548409-C-G

101587722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548445-G-A

101587722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548445-G-T

101587739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548461-G-A

101587739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548461-G-T

101587747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548469-A-G

101587754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548476-G-T

101587763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548491-G-T

101587768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548512-T-C

101587837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548580-G-A

101587837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548580-G-T

101587888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45548639-T-G

http://identifiers.org/hco/10/GRCh38#101588029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45548765-A-C

101588029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 45548765-A-G

101588036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45548772-G-A

101588206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 45548927-G-A

101588231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45548952-G-A

101588231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45548952-G-C

101588231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45548952-G-T

101588321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45549067-G-A

101588321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45549067-G-C

101588321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45549067-G-T

101588476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45549220-T-C

http://identifiers.org/hco/10/GRCh38#101588592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45549335-C-A

101588592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45549335-C-G

101588592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45549335-C-T

http://identifiers.org/hco/10/GRCh38#101588702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45549444-A-C

101588717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45549460-T-A

101588717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45549460-T-G

101588799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45549634-T-A

101588799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45549634-T-G

101588801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45549636-A-G

101588829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45549645-T-C

101588942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45549956-A-G

101589001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45550037-G-A

101589341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45550425-G-T

101594300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553055-T-C

101594308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553060-A-G

101594511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553216-T-A

101594511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553216-T-G

101594569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553253-T-C

http://identifiers.org/hco/10/GRCh38#101594802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45553493-C-A

101594805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553496-T-A

101594842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553534-T-C

101594843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553535-G-C

101595078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553760-T-C

101595078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553760-T-G

101595132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553806-C-T

101595199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553870-T-C

101595219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45553889-A-G

101595982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45554662-C-T

101596256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45554896-G-C

101596374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45555005-G-A

http://identifiers.org/hco/10/GRCh38#101596466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45555099-A-C

101596639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 45555278-A-G

101596640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45555279-G-A

101596648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45555287-G-A

http://identifiers.org/hco/10/GRCh38#101596835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45555615-C-A

101596950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45555744-C-T

101597092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45555886-G-A

101597163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45555957-C-T

101597548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45556340-C-T

101597724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45556521-A-G

101597746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45556543-G-A

101597781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45556581-G-A

101597978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 45556757-A-G

101598029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45556804-T-A

http://identifiers.org/hco/10/GRCh38#101598050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45556824-A-C

101598166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45556937-C-T

101598265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45557020-C-T

101598349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45557121-T-C

101598376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45557151-T-C

101598469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45557273-G-A

http://identifiers.org/hco/10/GRCh38#101598594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45557391-C-A

101599662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45558312-A-G

101599725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45558337-T-A

101599725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45558337-T-C

101599729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45558341-A-G

101599798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45558409-C-T

101599871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45558489-G-A

101599925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45558554-C-G

101599925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45558554-C-T

101600130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45558958-C-T

101600133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45558961-G-T

101600163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45559648-T-A

101600172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45559657-T-C

101600178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45559663-T-C

101600286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45559763-G-A

101600593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45560221-G-C

101600593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45560221-G-T

101600594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45560222-A-G

101600656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45560279-T-G

101600721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron variant
orthologous variants: 45560307-C-G

101600926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45560499-T-C

101600934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45560507-G-A

101601004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45560566-G-C

101601004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45560566-G-T

101601008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45560570-G-C

101601008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45560570-G-T

101601072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45560596-G-A

101601072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45560596-G-C

101601172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45560709-A-T

http://identifiers.org/hco/10/GRCh38#101601474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45561066-C-A

101601474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45561066-C-T

101601476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45561068-T-A

101601476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45561068-T-C

101601507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45561093-A-G

http://identifiers.org/hco/10/GRCh38#101601553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45561138-C-A

101601553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45561138-C-T

101601594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45561178-G-A

101601594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45561178-G-T

101601761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45561317-C-G

101601761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45561317-C-T

101602131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45561597-G-C

101604155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45562746-T-C

101604769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563282-A-T

101605099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563548-G-C

101605147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45563576-G-T

101605152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 45563581-G-C

101605161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45563590-C-G

101605161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45563590-C-T

101605177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 45563608-A-T

101605228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563639-C-T

101605231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563642-A-G

101605254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563665-G-A

101605254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563665-G-T

101606803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563849-A-G

101606966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563943-C-G

101606966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563943-C-T

101606986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45563961-A-T

http://identifiers.org/hco/10/GRCh38#101607416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#45564367-A-C

101607814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45564763-A-G

101608233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565098-C-T

101608252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565114-C-T

101608253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565115-G-A

101608253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565115-G-C

101608657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565273-A-G

101608699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565309-A-G

101608704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565314-T-C

101608715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565326-C-T

101608729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565340-T-A

101608729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565340-T-C

101608863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45565460-C-G

101609001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45565588-T-G

http://identifiers.org/hco/10/GRCh38#101609008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45565595-C-A

101609008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45565595-C-T

101609039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45565613-C-T

101609065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565638-G-A

101609065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565638-G-T

http://identifiers.org/hco/10/GRCh38#101609092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45565667-C-A

101609092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565667-C-G

101609092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565667-C-T

101609094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565669-G-A

101609094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565669-G-T

http://identifiers.org/hco/10/GRCh38#101609131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45565706-A-C

101609131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565706-A-G

101609131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565706-A-T

http://identifiers.org/hco/10/GRCh38#101609132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45565707-C-A

101609132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565707-C-G

101609132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565707-C-T

http://identifiers.org/hco/10/GRCh38#101609221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45565773-C-A

101609221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45565773-C-T

101609451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45565978-G-A

101609545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566008-G-A

http://identifiers.org/hco/10/GRCh38#101609578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45566026-C-A

101609610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566041-A-G

101609610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566041-A-T

http://identifiers.org/hco/10/GRCh38#101609623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45566054-C-A

101609623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566054-C-T

http://identifiers.org/hco/10/GRCh38#101609661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#45566079-C-A

101609661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45566079-C-T