113979392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 103645364-A-G

113979392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 103645364-A-T

113979412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 103645345-A-G

113979412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 103645345-A-T

113979413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 103645343-G-T

http://identifiers.org/hco/1/GRCh38#113979428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#103645328-C-A

113979471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 103645289-G-A

113979471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 103645289-G-T

http://identifiers.org/hco/1/GRCh38#113979758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103645028-A-C

113979943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103644863-G-A

113979943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103644863-G-C

113979943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103644863-G-T

113980159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103644703-T-C

113980192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103644673-C-T

113980367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103644516-G-A

113980367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103644516-G-T

113980568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 103644315-T-C

113980605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103644278-G-A

113980605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103644278-G-T

113980614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103644269-A-G

http://identifiers.org/hco/1/GRCh38#113980823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103644111-C-A

113980823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103644111-C-T

113980826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103644108-T-A

113980826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103644108-T-G

http://identifiers.org/hco/1/GRCh38#113980842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103644094-C-A

113980842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103644094-C-G

113980842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103644094-C-T

http://identifiers.org/hco/1/GRCh38#113980855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103644081-C-A

113980855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103644081-C-T

113980868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103644068-A-G

113980868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103644068-A-T

113980926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103644008-T-C

113981010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 103643916-A-G

113981344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103643582-T-C

113981347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103643579-G-A

113981846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103643088-A-T

113981888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103643043-T-C

113981919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103643016-T-A

113981919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103643016-T-C

http://identifiers.org/hco/1/GRCh38#113982008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103642933-C-A

113982008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103642933-C-T

http://identifiers.org/hco/1/GRCh38#113982155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103642803-C-A

113982155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103642803-C-T

113982170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103642792-C-T

http://identifiers.org/hco/1/GRCh38#113982204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103642758-C-A

113982204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103642758-C-T

113982296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103642668-C-T

http://identifiers.org/hco/1/GRCh38#113982348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103642619-A-C

113982348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103642619-A-T

113982349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103642618-T-A

113982349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103642618-T-C

113982921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103642083-A-G

http://identifiers.org/hco/1/GRCh38#113982966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103642052-C-A

113982989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103642025-C-G

113983281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103641789-C-G

113983281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103641789-C-T

113983450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103641624-G-A

http://identifiers.org/hco/1/GRCh38#113983775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103641305-C-A

113983804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103641282-C-T

113983836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103641250-G-A

http://identifiers.org/hco/1/GRCh38#113984177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103640899-A-C

113984227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103640844-G-A

113984227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103640844-G-T

113984867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103640291-T-C

113984921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103640246-T-C

113984991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103640174-A-G

113985024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103640138-C-T

113985068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103640094-T-A

113985068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103640094-T-C

113985073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103640089-C-G

113985142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103639809-T-C

113985237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103639716-C-T

113985305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103639579-G-A

113985339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103639524-T-C

113985561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103639174-C-G

113986155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103639128-T-G

113986904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103638540-A-G

http://identifiers.org/hco/1/GRCh38#113986949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103638496-C-A

113986949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103638496-C-T

113987172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103637757-G-A

http://identifiers.org/hco/1/GRCh38#113987515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103637524-C-A

113987515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103637524-C-T

113987523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103637516-G-A

113987546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103637493-T-C

113987550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103637489-C-G

113989855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103636307-C-G

113989855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103636307-C-T

113989919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103636276-G-A

113990479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635678-A-G

113990634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635536-T-C

113990848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635319-C-G

113990867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635305-G-T

113990982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635122-T-C

113990982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635122-T-G

113990988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635116-A-G

113991103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103635000-G-A

113991136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103634966-T-G

113991210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103634897-T-C

113991270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103634836-G-T

113992278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103630562-A-G

http://identifiers.org/hco/1/GRCh38#113999594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103627165-C-A

113999845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626925-T-C

114000123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626656-G-T

114000298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626471-C-T

114000302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626467-A-G

114000302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626467-A-T

114000426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626351-G-A

114000426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626351-G-C

114000639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626156-T-C

114000723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626110-T-C

114000815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103626039-C-G

114000971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625852-T-C

114001045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625765-A-G

114001061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625754-C-T

114001154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625661-T-C

114001294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625544-G-T

http://identifiers.org/hco/1/GRCh38#114001309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103625529-C-A

114001309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625529-C-T

114002326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625069-T-C

114002383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103625022-G-T

114002798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103624621-A-G

114002812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103624612-C-T

114002921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103624497-C-T

114003139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103624247-G-A

114003323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103624018-T-C

114003578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103623783-A-G

http://identifiers.org/hco/1/GRCh38#114003583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103623778-C-A

114003809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103623576-G-A

http://identifiers.org/hco/1/GRCh38#114003942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103623406-A-C

114004367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103622867-T-C

114007544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103621827-G-C

http://identifiers.org/hco/1/GRCh38#114007581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103621791-A-C

114007769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103621584-T-C

114007807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103621547-G-C

114007956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103621391-G-C

http://identifiers.org/hco/1/GRCh38#114008049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103621287-A-C

114008335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103620911-G-A

114008355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103620890-A-G

114008537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103620707-T-G

114008629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103620610-C-T

114008766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103620461-T-C

114011167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103616370-G-C

114011984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103615047-C-T

114012076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103614958-T-G

114012309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103614786-T-G

114012378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103614728-C-T

114012426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103614680-G-T

114012463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103614647-C-T

114012580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103614513-G-A

114014292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103604135-G-C

http://identifiers.org/hco/1/GRCh38#114015055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103603303-A-C

114015380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103602987-T-C

http://identifiers.org/hco/1/GRCh38#114015463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103602896-C-A

http://identifiers.org/hco/1/GRCh38#114015465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103602894-A-C

114016523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103601709-T-C

114016611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103601622-T-C

114016679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103601568-G-A

http://identifiers.org/hco/1/GRCh38#114017204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103600777-C-A

114017485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103600471-A-G

114017798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103600139-C-T

114017819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103600124-C-T

http://identifiers.org/hco/1/GRCh38#114018587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103597731-A-C

114018605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103597713-C-T

114018917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103597447-C-T

114018947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103597420-T-C

114022625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103596918-G-T

114022723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103596820-G-A

114022863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103596688-C-T

114022867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103596685-C-T

114022898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103596655-T-C

114026805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103594742-C-T

114026943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103594636-T-C

114027131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103594458-C-T

114027193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103594369-C-G

114027256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103594249-G-A

114027265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103594240-C-T

114027496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103593832-G-A

114032526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103591622-A-G

114032551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103591597-A-G

http://identifiers.org/hco/1/GRCh38#114032923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103591311-C-A

114032923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103591311-C-T

114032956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103591278-C-T

http://identifiers.org/hco/1/GRCh38#114032957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#103591277-C-A

http://identifiers.org/hco/1/GRCh38#114033110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#103591133-C-A

114033110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103591133-C-G

114033220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103591009-T-C

114033299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103590931-C-G

114033419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590803-T-C

114033419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590803-T-G

114033449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590771-G-T

114033478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103590744-G-T

114033507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590715-C-T

114033534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590688-G-T

114033562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590660-T-C

114033581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590641-T-C

http://identifiers.org/hco/1/GRCh38#114033632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#103590589-C-A

114033632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 103590589-C-T

114033742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590463-C-T

114033820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590373-T-C

114033820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590373-T-G

114033924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 103590262-A-T

http://identifiers.org/hco/1/GRCh38#114034749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103589980-C-A

114034857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103589873-G-A

114034959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103589773-A-G

114035032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103589699-G-A

114035114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103589625-A-G

114035172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103589574-T-C

114035180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103589558-G-C

114035180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103589558-G-T

http://identifiers.org/hco/1/GRCh38#114035347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103589403-C-A

http://identifiers.org/hco/1/GRCh38#114035348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#103589402-C-A

114035362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: non coding transcript exon variant
orthologous variants: 103589388-G-T

114035397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: non coding transcript exon variant
orthologous variants: 103589355-T-A

114035397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24956
most severe consequence: non coding transcript exon variant
orthologous variants: 103589355-T-C