http://identifiers.org/hco/1/GRCh38#36223191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126098649-A-C

36223217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126098620-A-G

36223804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126097047-C-T

36224128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126096760-C-T

36224185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, undefined
orthologous variants: 126096700-T-C

36224228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, undefined
orthologous variants: 126096648-G-A

36224324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, undefined
orthologous variants: 126096546-T-C

36224356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126096514-G-A

36224356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126096514-G-T

36224420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126096447-A-G

36224420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126096447-A-T

36224448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 126096419-A-G

36224516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126096350-G-A

36224516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126096350-G-T

http://identifiers.org/hco/1/GRCh38#36224520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126096346-C-A

36224527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126096339-A-G

36224565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126096300-C-T

36224650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126096215-T-C

http://identifiers.org/hco/1/GRCh38#36224677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126096189-C-A

36224677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126096189-C-G

36224683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 126096183-C-T

http://identifiers.org/hco/1/GRCh38#36224728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126096138-A-C

36224738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126096129-T-C

http://identifiers.org/hco/1/GRCh38#36224884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#126095972-C-A

http://identifiers.org/hco/1/GRCh38#36225119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126095707-C-A

36225119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126095707-C-G

36225175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126095655-G-A

36225175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126095655-G-T

http://identifiers.org/hco/1/GRCh38#36225216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126095614-C-A

36225309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126095533-T-A

36225309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126095533-T-C

36226710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126093632-A-G

36226785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126093572-T-A

36226810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126093547-T-G

36259507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126088085-A-G

36259520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126088070-A-G

36263414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126085209-T-A

36263499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126085139-C-T

36265313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126083539-G-A

36267086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126082589-A-G

36267135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126082520-C-T

36267142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126082513-C-T

36267154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126082502-T-G

36267201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126082458-A-G

36267397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126082313-A-G

http://identifiers.org/hco/1/GRCh38#36272271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126081849-A-C

36272536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126081594-C-T

36282592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126080334-G-T

36282624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126080302-A-G

36282657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126080269-T-A

http://identifiers.org/hco/1/GRCh38#36282660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126080266-C-A

36282664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126080262-G-A

36282666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126080260-C-G

36282666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 126080260-C-T

36282709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126080214-G-A

36282709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126080214-G-C

36282709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126080214-G-T

36282710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126080213-T-G

36282762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126080166-A-G

36282789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126080153-G-A

36282789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126080153-G-T

http://identifiers.org/hco/1/GRCh38#36282801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126080141-C-A

36283012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126080009-A-G

36283256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126079767-C-G

36283256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126079767-C-T

36283401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126079635-G-A

http://identifiers.org/hco/1/GRCh38#36283420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126079615-C-A

36283928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126079084-A-G

36286383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126074590-C-T

36286537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074436-G-A

36286539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126074434-C-T

36286548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126074425-C-T

36286558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074415-A-G

http://identifiers.org/hco/1/GRCh38#36286600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126074373-C-A

36286600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074373-C-T

36286604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074369-C-T

36286628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074345-G-A

36286638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126074335-A-G

36286638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126074335-A-T

36286639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074334-C-T

36286694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074279-G-A

36286791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126074182-C-T

36286792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074181-C-T

36286857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126074116-C-T

36286886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074087-G-A

36286918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074052-A-G

36286942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074031-G-A

36286942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074031-G-T

36286961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074012-C-G

36286961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126074012-C-T

36287004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126073969-G-A

36287012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126073961-G-A

36287014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126073959-C-T

http://identifiers.org/hco/1/GRCh38#36287024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126073949-C-A

36287068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126073905-A-G

36287083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126073890-T-C

36287083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126073890-T-G

36287094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126073879-G-A

36287094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 126073879-G-C

36287104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126073869-G-A

http://identifiers.org/hco/1/GRCh38#36287158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126073815-A-C

36287215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126073758-G-A

36287251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126073722-G-A

36287342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126073636-T-A

36287347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126073631-T-G

36287373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126073604-A-G

36287418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126073572-A-G

http://identifiers.org/hco/1/GRCh38#36287419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126073571-C-A

36287419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126073571-C-T

36287508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126073492-T-C

36287590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 126073409-A-G

36287929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126073119-G-A

36287929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126073119-G-C

36287949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126073101-G-T

36288400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126072930-A-G

36288464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126072878-T-C

36288700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126072641-G-A

36288700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126072641-G-C

36288745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126072597-A-T

36289050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126072358-T-C

36289079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126072329-A-G

36289346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126072071-G-A

http://identifiers.org/hco/1/GRCh38#36289821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126071594-A-C

36289821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126071594-A-T

http://identifiers.org/hco/1/GRCh38#36289843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126071572-C-A

36289843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126071572-C-G

36289843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126071572-C-T

http://identifiers.org/hco/1/GRCh38#36289884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126071543-C-A

36289884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126071543-C-G

36290003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126071439-C-G

36290003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126071439-C-T

36290098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126071333-C-T

36290887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126071167-T-C

36291124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126070898-G-T

36291338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126070182-G-A

http://identifiers.org/hco/1/GRCh38#36291537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126069984-C-A

36291537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126069984-C-T

36292188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126069322-C-G

http://identifiers.org/hco/1/GRCh38#36292793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126069060-A-C

36292793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126069060-A-G

http://identifiers.org/hco/1/GRCh38#36292823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126069030-C-A

36292823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126069030-C-T

36292868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126068985-T-C

36293251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126068839-A-T

36293799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126067363-G-T

36294633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126066537-C-T

36295343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126066190-C-T

36295391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126066144-G-A

36295418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126066116-C-G

36296533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 126065720-T-G

http://identifiers.org/hco/1/GRCh38#36296619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126065636-C-A

36296619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 126065636-C-T

36297066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126065114-T-C

36297105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126065074-T-C

36297147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126065041-C-T

36297189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126065009-T-C

36300134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, undefined
orthologous variants: 126062472-T-C

36300259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, undefined
orthologous variants: 126062349-T-G

http://identifiers.org/hco/1/GRCh38#36300585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126061926-A-C

36301289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126061114-T-G

36301290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126061113-T-C

36301512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060906-G-T

36301670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: missense variant
orthologous variants: 126060748-A-T

36301741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060677-A-G

36301770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060650-T-A

36301776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060644-G-A

36301776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060644-G-T

http://identifiers.org/hco/1/GRCh38#36301794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126060626-A-C

36301794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060626-A-G

36301800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060620-G-A

36301800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060620-G-T

36301860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060571-C-T

36301936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060505-G-C

36301947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060494-T-G

36302541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126060168-T-G

36302783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126059926-T-A

36302793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126059917-G-T

36303559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126059584-C-T

36303560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126059583-G-A

36303560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126059583-G-C

http://identifiers.org/hco/1/GRCh38#36303595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059553-A-C

36303702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron variant
orthologous variants: 126059464-T-C

36303843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 126059361-C-T

36303844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, missense_variant
orthologous variants: 126059360-C-G

36303844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, missense_variant
orthologous variants: 126059360-C-T

36303849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 126059355-C-G

36303870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 126059334-T-C

36303888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, missense_variant
orthologous variants: 126059316-C-G

36303909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 126059295-C-G

36303909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 126059295-C-T

36303919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, missense_variant
orthologous variants: 126059285-C-T

36303949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, missense_variant
orthologous variants: 126059255-A-G

36303958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, missense_variant
orthologous variants: 126059246-G-A

36303958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, missense_variant
orthologous variants: 126059246-G-T

http://identifiers.org/hco/1/GRCh38#36303997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059207-A-C

36303997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, missense_variant
orthologous variants: 126059207-A-G

36304016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: intron_variant, undefined
orthologous variants: 126059188-A-G

36304020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059184-G-A

36304020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059184-G-T

http://identifiers.org/hco/1/GRCh38#36304021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059183-C-A

http://identifiers.org/hco/1/GRCh38#36304042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059162-C-A

36304042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059162-C-T

http://identifiers.org/hco/1/GRCh38#36304043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059161-C-A

36304047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059157-G-C

36304047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059157-G-T

http://identifiers.org/hco/1/GRCh38#36304090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059119-A-C

36304090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059119-A-G

http://identifiers.org/hco/1/GRCh38#36304123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: -C-A

36304123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: -C-G

http://identifiers.org/hco/1/GRCh38#36304127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059083-C-A

36304127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059083-C-G

http://identifiers.org/hco/1/GRCh38#36304142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059068-C-A

36304142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059068-C-T

36304158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059053-G-A

http://identifiers.org/hco/1/GRCh38#36304182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059023-C-A

36304182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059023-C-T

http://identifiers.org/hco/1/GRCh38#36304190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059015-C-A

36304190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059015-C-T

http://identifiers.org/hco/1/GRCh38#36304199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126059004-C-A

36304199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126059004-C-T

http://identifiers.org/hco/1/GRCh38#36304205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058996-A-C

36304205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058996-A-G

36304205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058996-A-T

http://identifiers.org/hco/1/GRCh38#36304244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058979-C-A

36304244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058979-C-T

36304284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058946-T-G

36304292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058938-G-A

36304292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058938-G-T

http://identifiers.org/hco/1/GRCh38#36304297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058936-C-A

36304297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058936-C-G

36304297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058936-C-T

http://identifiers.org/hco/1/GRCh38#36304298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058935-A-C

36304298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058935-A-T

36304301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058932-G-T

36304303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058930-T-A

36304303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058930-T-G

36304305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058928-G-A

36304305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058928-G-T

36304365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058841-T-C

36304377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058829-T-C

http://identifiers.org/hco/1/GRCh38#36304413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058798-C-A

36304413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058798-C-T

36304414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058797-T-A

36304414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 126058797-T-C

36304485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 126058733-A-T

36304491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 126058727-A-T

http://identifiers.org/hco/1/GRCh38#36304493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058721-A-C

36304493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 126058721-A-G

36304493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 126058721-A-T

36304510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 126058704-A-T

36304575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058642-G-T

36304582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058635-A-G

http://identifiers.org/hco/1/GRCh38#36304605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058613-C-A

36304618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058600-T-A

36304666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058553-T-G

36304707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058514-T-C

http://identifiers.org/hco/1/GRCh38#36304746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058481-C-A

36304746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058481-C-T

36304762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058466-T-C

36304812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058418-A-G

http://identifiers.org/hco/1/GRCh38#36304896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058328-A-C

36304897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058327-A-G

36304978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058247-G-T

36304995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058224-T-A

36305034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058189-A-G

36305111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058119-G-C

36305111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058119-G-T

36305114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058116-G-T

36305116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058114-G-A

36305117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058113-G-A

36305117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058113-G-T

36305120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058110-G-A

36305135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058095-A-G

http://identifiers.org/hco/1/GRCh38#36305144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058088-C-A

36305144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058088-C-T

36305149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058083-A-G

36305161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058071-T-A

36305161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058071-T-C

36305164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058068-G-T

http://identifiers.org/hco/1/GRCh38#36305165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#126058067-C-A

36305165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058067-C-T

36305194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058039-T-A

36305194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058039-T-C

36305205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058029-C-G

36305205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126058029-C-T

36305287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22964
most severe consequence: 3 prime UTR variant
orthologous variants: 126057948-A-G