3581271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3797101-A-T

http://identifiers.org/hco/16/GRCh38#3581354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3797172-A-C

3581354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3797172-A-G

http://identifiers.org/hco/16/GRCh38#3581453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3797253-C-A

3581537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3797299-G-A

3581537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3797299-G-T

3581640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3797375-A-G

http://identifiers.org/hco/16/GRCh38#3581903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3797512-C-A

3581903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3797512-C-T

3582166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3797562-G-A

3582431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3797774-T-C

3582432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3797775-A-G

3582454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 3797797-A-T

3582479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3797822-G-T

3582480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3797823-G-A

3582489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3797832-C-T

3582613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3797956-G-T

3582626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3797969-T-C

3582626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3797969-T-G

3582666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3798012-T-C

3582685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3798028-G-A

3582685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3798028-G-T

3582696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 3798039-G-A

3582696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 3798039-G-T

3582714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798052-A-T

3582762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798103-T-A

3582770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798111-G-T

3582775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798116-G-A

3582775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798116-G-C

3582924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798284-G-A

3582954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798314-C-G

3582954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798314-C-T

http://identifiers.org/hco/16/GRCh38#3582957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3798317-C-A

http://identifiers.org/hco/16/GRCh38#3582980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3798337-C-A

3582980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798337-C-T

3583148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3798496-T-A

3583148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3798496-T-C

3583373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense variant
orthologous variants: 3798721-C-T

3583384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense variant
orthologous variants: 3798732-C-G

3583427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: stop gained
orthologous variants: 3798775-G-C

3584552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron variant
orthologous variants: 3799253-G-A

3584593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron variant
orthologous variants: 3799287-G-C

3584652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron variant
orthologous variants: 3799342-G-A

3584652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron variant
orthologous variants: 3799342-G-T

http://identifiers.org/hco/16/GRCh38#3584653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3799343-C-A

3584653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron variant
orthologous variants: 3799343-C-T

http://identifiers.org/hco/16/GRCh38#3588852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3802740-A-C

3588852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3802740-A-G

3588855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3802743-G-A

3588855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3802743-G-T

3588862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3802750-G-T

3588863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3802751-G-A

3588863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3802751-G-T

3588959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3802818-G-C

3588991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3802844-T-A

3589166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3802989-T-C

3589186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3803009-G-C

3589319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3803139-T-C

3589398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3803215-G-C

3589398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3803215-G-T

3589511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3803322-T-C

3589762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3803531-G-A

http://identifiers.org/hco/16/GRCh38#3589788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3803557-C-A

3589788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3803557-C-T

3589844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3803613-C-T

3589924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3803693-G-A

3589924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3803693-G-T

3589997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3803763-A-G

http://identifiers.org/hco/16/GRCh38#3590130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3803896-A-C

3590317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3804077-C-T

3590589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3804343-C-T

http://identifiers.org/hco/16/GRCh38#3590647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3804401-C-A

3590647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3804401-C-T

3590681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3804435-A-G

3590701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3804455-A-T

3590752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3804494-G-A

3590793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3804535-G-C

3590999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3804732-A-G

3591073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 3804806-A-T

3591149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3804882-G-A

3591187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3804920-T-C

3591187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3804920-T-G

3591243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3804973-G-A

3591243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3804973-G-T

3591272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3805002-A-G

http://identifiers.org/hco/16/GRCh38#3591342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3805073-C-A

3591342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805073-C-T

3591389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805096-G-C

http://identifiers.org/hco/16/GRCh38#3591422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3805127-C-A

3591546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805210-C-G

3592576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805652-G-A

3592576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805652-G-T

3592594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805662-A-G

3592594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805662-A-T

http://identifiers.org/hco/16/GRCh38#3592660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3805729-C-A

3592660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805729-C-G

3592716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3805796-C-T

3592738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3805818-G-A

3592785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3805865-G-A

3592815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3805895-A-G

http://identifiers.org/hco/16/GRCh38#3592832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3805912-C-A

3592832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3805912-C-G

3592832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3805912-C-T

3592860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3805940-G-A

3594444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3806828-C-T

3595457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807870-G-T

3595493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807915-A-G

3595493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807915-A-T

http://identifiers.org/hco/16/GRCh38#3595502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3807939-C-A

3595502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807939-C-T

http://identifiers.org/hco/16/GRCh38#3595525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3807987-C-A

3595525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807987-C-T

http://identifiers.org/hco/16/GRCh38#3595665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3808152-A-C

3595806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808256-T-C

http://identifiers.org/hco/16/GRCh38#3596013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3808453-C-A

3596013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808453-C-T

3596029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808464-G-A

3596029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808464-G-T

http://identifiers.org/hco/16/GRCh38#3596058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3808494-C-A

3596058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808494-C-T

http://identifiers.org/hco/16/GRCh38#3596061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3808497-C-A

3596061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808497-C-T

3596062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808498-G-A

3596062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808498-G-T

3596067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808503-A-G

3596081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808518-G-A

3596081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808518-G-T

3596178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3808577-G-A

3596178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3808577-G-T

3596187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3808586-G-A

3596187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3808586-G-T

3596356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 3808755-G-A

3596356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 3808755-G-C

3596356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 3808755-G-T

3596366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 3808765-G-C

3596366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 3808765-G-T

3596431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3808817-C-T

3596439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3808825-G-A

3596439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3808825-G-T

3596463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3808848-A-G

3596463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3808848-A-T

3596540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808877-A-G

3597087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809099-C-T

3597242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809217-G-A

3597242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809217-G-T

http://identifiers.org/hco/16/GRCh38#3597291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3809257-C-A

3597291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809257-C-T

http://identifiers.org/hco/16/GRCh38#3597293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3809259-C-A

3597293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809259-C-T

3597311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809276-G-A

3597311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809276-G-T

3597344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809296-A-G

3597345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809297-A-G

3597362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809319-T-A

3597362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809319-T-C

3597363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809320-G-A

3597363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809320-G-T

3597391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3809348-C-G

3597391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3809348-C-T

3597460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3809417-G-A

3597501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3809458-G-A

3597656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3809613-G-C

3597656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3809613-G-T

http://identifiers.org/hco/16/GRCh38#3597667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3809624-C-A

3597667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3809624-C-G

3597667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3809624-C-T

http://identifiers.org/hco/16/GRCh38#3597843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3809826-C-A

3597843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3809826-C-T

3597988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3809974-T-G

http://identifiers.org/hco/16/GRCh38#3598116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3810082-C-A

3598116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3810082-C-G

3598116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 3810082-C-T

http://identifiers.org/hco/16/GRCh38#3598146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3810120-C-A

3598146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3810120-C-G

3598146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3810120-C-T

3598202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3810178-G-T

3598625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3810524-G-A

3598713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3810595-G-A

3599172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3811567-C-T

3599243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3811662-G-A

3599543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3811903-T-A

3600375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3812323-G-A

http://identifiers.org/hco/16/GRCh38#3600494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3812420-C-A

3600494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3812420-C-T

3600553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3812475-T-C

http://identifiers.org/hco/16/GRCh38#3601154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3812747-C-A

3601154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3812747-C-T

3601169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3812762-T-A

3601169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3812762-T-C

3601220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3812810-C-G

3601220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3812810-C-T

http://identifiers.org/hco/16/GRCh38#3601266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3812851-A-C

3601266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3812851-A-G

3601408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3812981-T-A

3601408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3812981-T-G

3601413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3812983-G-T

3601561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813120-G-A

3601561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813120-G-T

3601620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813142-G-T

3601638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813161-G-A

3601638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813161-G-T

3601761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813295-T-C

3601761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813295-T-G

3601771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813302-C-G

http://identifiers.org/hco/16/GRCh38#3601784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3813315-A-C

3601784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813315-A-G

3601800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813331-G-C

3601875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813400-T-C

3601875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813400-T-G

3602040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813535-G-C

3602040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3813535-G-T

http://identifiers.org/hco/16/GRCh38#3602144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3813584-C-A

3602144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3813584-C-T

3602455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3813888-T-C

3602500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3813937-C-T

3602619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3814017-C-T

3606319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3816846-C-G

3606342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3816869-G-T

3606348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3816874-G-T

3606387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3816912-C-T

3606449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3816958-G-T

3606516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3817024-T-C

3606516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3817024-T-G

3606538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3817046-G-A

3606538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3817046-G-T

http://identifiers.org/hco/16/GRCh38#3606681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3817192-C-A

3606681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3817192-C-T

3606693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3817204-C-G

3606693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3817204-C-T

3607011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3817447-C-T

3607236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3817645-A-G

http://identifiers.org/hco/16/GRCh38#3607246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3817654-C-A

3607246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3817654-C-T

3608347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3818694-T-G

3608437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3818773-T-A

3608437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3818773-T-G

3608483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3818822-T-G

http://identifiers.org/hco/16/GRCh38#3608768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3819104-C-A

3608768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3819104-C-G

3608861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3819196-G-A

3608880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3819215-G-A

3608958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3819289-G-A

3608958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3819289-G-C

3608977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3819308-C-T

http://identifiers.org/hco/16/GRCh38#3609074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3819387-C-A

3609074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3819387-C-G

3609074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3819387-C-T

http://identifiers.org/hco/16/GRCh38#3609507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3819484-C-A

3609544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 3819521-A-G

http://identifiers.org/hco/16/GRCh38#3609626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3819606-C-A

3609853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3819783-G-T

3610377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3820532-T-C

3610540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3820694-G-C

3610573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3820727-T-C

3610573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3820727-T-G

3610751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3820855-C-T

3610877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3820990-G-A

3610954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3821054-C-G

3611524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3821558-T-A

3611524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3821558-T-C

3611544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3821580-G-A

3611544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3821580-G-T

3611596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23845
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 3821632-C-G