http://identifiers.org/hco/4/GRCh38#177442535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#53964667-C-A

177442535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53964667-C-G

177442542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 53964660-G-C

177442582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 53964592-G-A

177442582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 53964592-G-T

177442586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964588-T-C

http://identifiers.org/hco/4/GRCh38#177442605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53964552-A-C

177442605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964552-A-G

177442623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53964531-G-A

177442885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53964261-T-C

177443043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53964098-C-T

http://identifiers.org/hco/4/GRCh38#177443063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#53964079-C-A

177443063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53964079-C-T

177443576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53963797-G-C

177443805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53963647-A-G

177445737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962464-T-C

http://identifiers.org/hco/4/GRCh38#177445742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53962458-C-A

177445752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962450-A-G

http://identifiers.org/hco/4/GRCh38#177445755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53962447-A-C

http://identifiers.org/hco/4/GRCh38#177445760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53962442-C-A

177445760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962442-C-T

177445804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962399-T-C

177446334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962073-C-T

177446398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53962045-C-T

177446501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53961967-G-A

177446554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53961916-G-A

177446618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53961853-C-T

177446680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53961579-T-C

177447123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53961132-T-C

http://identifiers.org/hco/4/GRCh38#177447390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53960866-A-C

http://identifiers.org/hco/4/GRCh38#177447858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53960403-A-C

177451908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53960039-A-G

177452534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959803-C-T

177452782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959560-T-C

177452935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959404-G-T

177452962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53959375-T-G

177453468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53958879-T-C

http://identifiers.org/hco/4/GRCh38#177453520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53958834-A-C

177455418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53950508-T-A

177455581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53950337-G-A

177455769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53950151-A-G

177456102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53949833-G-A

177456103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53949832-C-G

177456332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53949535-C-T

http://identifiers.org/hco/4/GRCh38#177456525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53949366-C-A

177456525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53949366-C-G

177463818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53948193-T-C

177465425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53945915-A-G

177465555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53945796-C-G

177465637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53945714-C-G

177466131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53945511-G-A

177466131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53945511-G-C

177466261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53945388-T-C

177466557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53945333-T-A

177466703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53945190-G-A

177466896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53944193-C-T

177466927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53944163-A-G

177467164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53943930-G-A

177467315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53943772-G-C

http://identifiers.org/hco/4/GRCh38#177467326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53943761-C-A

177467419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53943678-A-G

177467444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53943656-G-C

http://identifiers.org/hco/4/GRCh38#177467688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53943521-A-C

177468222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53943150-A-G

177468236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53943138-G-A

177468269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53943100-A-G

177468605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53942755-T-A

177469012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53942318-A-G

177469167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53942179-A-G

177469184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53942162-A-G

177469287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53942058-A-G

177469470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53941886-T-C

177469607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53941751-T-G

http://identifiers.org/hco/4/GRCh38#177478292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53939269-A-C

177478302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53939259-G-A

177478302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53939259-G-C

177478492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53939072-G-T

http://identifiers.org/hco/4/GRCh38#177478505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53939059-A-C

177478603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53938965-G-A

177479251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53938327-G-T

177479326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53938255-T-A

177479696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53937872-G-A

177479817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53937750-T-G

177479871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53937687-G-A

177480003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53937572-A-G

177480008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53937567-C-T

177480169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53937396-T-C

177480562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53936769-G-C

177480898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53936408-T-C

177481118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53936204-T-C

177481179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53936143-C-T

177481298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53936028-A-G

177482923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53935465-A-G

177483449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53934976-G-A

177483449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53934976-G-T

177484877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53933743-G-C

177484884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53933736-C-T

177485118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53933488-A-G

177486138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53932281-G-A

177486246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53932171-G-A

177486300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53932117-G-A

http://identifiers.org/hco/4/GRCh38#177486520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53931910-C-A

177486558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53931875-C-T

177487845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53927394-T-A

177488190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53927055-C-T

177488562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53926731-A-G

177488562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53926731-A-T

177489140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53926068-G-C

177489334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925863-G-A

177489336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925861-C-T

177489379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925818-T-C

177489493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925701-T-C

177489614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925577-G-A

177489669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925525-T-C

177489673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925521-G-A

177489716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925478-T-A

177489716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925478-T-G

177489763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925434-G-A

177489789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925404-A-G

177489839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925353-T-C

177489949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925252-G-A

177490066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53925164-C-G

177490517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53924775-T-G

177490573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53924720-T-C

177491043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53923258-T-C

177491354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53922729-A-G

177491398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53922683-C-T

177491457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53922642-C-G

177491525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53922576-A-T

177491538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53922563-A-G

177491621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53922480-G-A

177491671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53922436-T-C

177491787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53922324-A-T

177493227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53921714-T-C

http://identifiers.org/hco/4/GRCh38#177493446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53921512-C-A

177493589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53921380-C-T

177493754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53921196-C-T

177493849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53921109-G-C

177493962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53921005-G-A

177493973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920994-C-G

177494061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920915-T-C

177494061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920915-T-G

177494099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920884-G-A

177494099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920884-G-T

177494107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920875-T-C

177494175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920819-T-G

177494212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920782-G-T

177494273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920721-C-T

177494427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920567-G-A

177494427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920567-G-T

http://identifiers.org/hco/4/GRCh38#177494480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53920513-C-A

177494480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920513-C-G

177494546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920447-G-A

177494547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920446-T-A

177494547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920446-T-C

177494846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920159-G-T

177494847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53920158-A-T

http://identifiers.org/hco/4/GRCh38#177496854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53919580-A-C

177496893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53919540-G-A

177497099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53919333-G-A

177497169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53919264-G-T

177497188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53919245-C-G

177497304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53919132-C-T

177497346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53919090-C-T

177497539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918891-A-T

177497616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918822-T-C

177497619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918819-C-T

http://identifiers.org/hco/4/GRCh38#177497681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53918762-C-A

177497698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918745-A-G

177497809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918637-T-C

177497833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918613-C-T

177497931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918530-T-C

http://identifiers.org/hco/4/GRCh38#177498074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53918443-C-A

177498074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918443-C-T

177498090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918427-C-T

177498107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918411-T-C

177498131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918387-T-G

177498160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918369-A-T

177498164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918365-G-T

177498191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918338-A-T

http://identifiers.org/hco/4/GRCh38#177498192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53918337-C-A

177498192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918337-C-T

177498304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918224-T-C

177498350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918180-G-C

177514495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53918140-A-G

177514845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53917028-A-G

177514870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53917005-A-G

177514916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53916958-T-C

177515006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53916833-A-G

177515054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53916786-A-G

177515057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53916783-C-T

177515479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53916655-A-G

http://identifiers.org/hco/4/GRCh38#177515893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53916590-C-A

177516023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53916468-T-G

177516173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53916319-C-T

177517047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53916089-T-C

177517219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53915935-G-A

177517521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53915136-C-T

177517600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53915049-G-A

177517823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53914840-G-A

177517972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53914691-A-G

177517972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53914691-A-T

177518038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53914641-A-G

177518167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53914515-A-G

177518478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53914217-C-T

http://identifiers.org/hco/4/GRCh38#177518496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53914190-A-C

177518496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53914190-A-T

177518541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53914150-C-T

http://identifiers.org/hco/4/GRCh38#177528282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53903034-A-C

177528443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53902871-G-C

http://identifiers.org/hco/4/GRCh38#177528467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53902848-C-A

177528633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53902721-A-T

177528634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53902720-A-G

177528696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53902658-A-G

177528759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53902596-A-G

177529037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53902339-A-G

http://identifiers.org/hco/4/GRCh38#177530750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53901069-A-C

177530801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53901010-T-G

177530880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53900947-A-G

177530884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53900943-G-A

177530884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53900943-G-T

177530912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53900913-G-A

177531008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53900823-A-G

177531273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53900524-A-G

177531304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53900495-T-C

177531723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53900076-C-T

177531960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53899840-C-G

http://identifiers.org/hco/4/GRCh38#177531976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53899824-A-C

177531976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53899824-A-G

177532067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53899740-G-A

177532067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53899740-G-C

177532216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53899621-T-C

177533089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53898756-T-A

177533138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53898714-T-C

177535897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53897810-G-A

177536134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53897559-T-C

177539003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53897022-T-C

177539279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896737-A-G

177539301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896716-T-C

177540085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896210-C-T

177540130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53896165-T-C

177542211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53895267-G-A

177542445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53895036-G-T

http://identifiers.org/hco/4/GRCh38#177542478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53895008-C-A

177544127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893189-C-T

177544158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893158-G-T

177544159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893157-C-T

177544189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893130-C-G

177544291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53893029-A-G

177544344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892959-T-A

177544350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892950-T-C

177544354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892946-T-C

177544388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892908-G-A

177544716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892725-A-G

177544769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892671-G-A

177544870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892580-C-T

http://identifiers.org/hco/4/GRCh38#177544886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53892564-C-A

177544886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892564-C-T

177544988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892448-T-A

177545193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892264-T-C

177545252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53892202-T-C

177545676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53891807-A-G

177545718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53891719-A-G

177545810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53891630-T-A

177545878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53891562-G-T

177546077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53891373-T-C

177546113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53891332-G-T

177546240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53891205-A-G

177550098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53890843-A-T

177550101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53890840-A-T

177553339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53887275-T-A

177553470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53887153-G-T

http://identifiers.org/hco/4/GRCh38#177553532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53887091-A-C

177553644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886981-G-T

177553792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886836-T-C

177553798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886830-C-T

177553823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886805-T-C

177553874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886733-T-C

177553909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886703-T-C

177553982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886628-A-G

177555871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886051-T-C

177555894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53886028-C-T

177556215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53885706-A-G

177556327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53885613-C-T

177556343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53885597-A-G

177556659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53885224-G-T

http://identifiers.org/hco/4/GRCh38#177556749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53885136-C-A

177557190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53885039-T-G

177558503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884842-C-T

http://identifiers.org/hco/4/GRCh38#177558524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53884821-C-A

177558668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884691-A-G

http://identifiers.org/hco/4/GRCh38#177558875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53884486-C-A

177558875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884486-C-T

177559396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53884008-G-A

177559492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53883912-C-T

177559493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53883911-C-T

177559513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53883891-C-T

177559616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53883783-A-G

177559628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53883771-C-T

177559761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53883681-C-T

177560120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53883602-G-A

177560379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53883329-T-A

177562080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53881108-G-A

177562227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53880957-T-C

177562227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53880957-T-G

177567922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53877350-T-C

177568422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53876311-A-T

177568435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53876298-G-A

177568455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53876278-C-T

177568581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53876148-A-G

177568649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875996-T-A

177568649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875996-T-C

177569125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53875528-T-C

177569560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874718-A-G

177569623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874655-T-C

177569772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874506-C-G

177569830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874414-T-G

177570059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53874186-T-G

177570623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873544-A-G

177570647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873510-G-C

177570658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873478-T-C

http://identifiers.org/hco/4/GRCh38#177570660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53873476-C-A

177570660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873476-C-T

http://identifiers.org/hco/4/GRCh38#177570754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53873380-A-C

177570895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873251-T-C

177570948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873196-T-A

177570948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53873196-T-C

177571723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53872734-A-G

177572081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53872438-G-A

177572107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53872416-G-T

177572310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53871811-G-A

177572310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53871811-G-C

177572332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53871789-C-T

177574536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53869934-T-C

177574642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53869825-G-A

177574802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53869679-G-A

177574852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53869630-G-A

177574852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53869630-G-C

177575021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53869412-G-A

177575029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53869404-A-G

177575257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53869138-G-A

177575458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53868952-C-G

177575458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53868952-C-T

177575542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53868869-A-G

177575631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53868756-T-C

177575813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53868595-C-G

177575841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53868568-G-T

177575851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53868558-C-G

177575883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53868525-C-T

http://identifiers.org/hco/4/GRCh38#177576026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53867946-C-A

177576026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53867946-C-G

177576026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53867946-C-T

177576112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53867855-G-T

177578379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866991-A-G

177578516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866850-T-C

177578518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866848-A-G

177578519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866847-T-C

177578617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866759-A-G

177578637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866736-C-T

177578728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866610-T-G

177578759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866581-A-G

177578793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866560-T-C

177578843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866512-C-T

177578848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866507-A-T

177578901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866436-T-C

177578951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866396-T-A

177579104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53866271-G-A

177579433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53865951-T-C

177579510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53865869-A-G

177579537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53865842-A-G

http://identifiers.org/hco/4/GRCh38#177579749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53865395-C-A

177580024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53865132-C-G

177580195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53864963-G-T

177580333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53864827-A-G

177580548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53864634-T-C

177580656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53864528-G-A

177580735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53864461-A-G

177580819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53864375-T-G

177581029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53864225-T-A

177581140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53864125-T-C

177581161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53864111-T-C

177581640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53863976-G-A

177581773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53863850-C-T

177581941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53863690-T-C

177581944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53863687-A-T

177581971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53863652-G-T

177582014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53863231-G-A

177582482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53862778-G-A

177582510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53862750-G-T

http://identifiers.org/hco/4/GRCh38#177582892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53862227-C-A

177582892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53862227-C-G

177582927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53862191-T-G

177583023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53862095-T-C

177583308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53861779-T-C

177583557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53861546-C-T

177584175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53861024-C-G

http://identifiers.org/hco/4/GRCh38#177584375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53860834-A-C

177584375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53860834-A-G

177584381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53860829-T-G

http://identifiers.org/hco/4/GRCh38#177584622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53860603-C-A

177584642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53860583-A-G

177584682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53860536-G-A

177585431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53859398-T-C

177585506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53859343-G-A

177585655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53858802-A-G

177585667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53858790-G-A

177585697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53858759-A-G

177585799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53858661-T-C

http://identifiers.org/hco/4/GRCh38#177585868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53858581-C-A

177585909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53858549-A-G

177586140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53858254-C-T

177586171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53858220-C-G

177586171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53858220-C-T

177586280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53858111-C-G

177586776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53857629-A-G

177586817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53857590-C-T

177586988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53857437-T-C

177587210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53857224-C-T

177587218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53857216-G-A

177587237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53857197-G-A

177587261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53857173-T-A

177587350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53857080-G-C

177587648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53856786-G-A

177587914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53856466-T-C

177588357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53856024-G-A

177588914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53852087-A-G

177589047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851967-C-T

177589308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851690-C-T

177589653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53851015-T-C

177589728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850935-G-A

177589923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850752-T-A

177590173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850503-G-A

177590197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850480-T-C

177590566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850136-T-C

177590622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53850081-G-A

177594376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53849300-A-G

177594684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848965-A-T

177594694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848954-T-C

177594856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848795-G-A

177594972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848680-G-T

177594985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848667-T-C

177595200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848470-C-T

177595268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848403-A-T

177595517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53848165-T-C

177595690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847999-T-A

177595792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847884-G-A

177595792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847884-G-C

177596118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53847562-T-C

177597613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53846191-T-C

177598352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53846036-A-G

177598484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53845926-A-G

177598810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53845641-G-A

177598878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53845573-A-G

177598891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53845560-C-T

177598969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53845461-C-T

177598983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53845445-T-C

177599739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53845121-A-T

177599868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844970-A-T

177599910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844933-T-G

177600127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844747-A-G

177600127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844747-A-T

177600207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844671-A-T

http://identifiers.org/hco/4/GRCh38#177600271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53844615-A-C

177600271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844615-A-T

177600808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844391-C-T

177600823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844378-G-A

177600886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844311-T-C

177600901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844296-A-T

177601029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844275-T-C

177601115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844203-C-T

177601235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53844100-A-G

177601364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53843969-T-A

http://identifiers.org/hco/4/GRCh38#177601695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53843669-A-C

177604032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53840856-C-T

177604035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53840853-T-C

177604152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53840732-T-C

177604319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53840538-C-T

177604401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53840459-C-T

177604450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53840413-A-G

http://identifiers.org/hco/4/GRCh38#177604663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53840310-A-C

177604770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53840211-T-C

177604776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53840205-A-G

177604800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53840182-T-C

http://identifiers.org/hco/4/GRCh38#177604887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53840093-A-C

177604993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53839754-T-C

177605617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53839120-T-C

177605655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53839081-T-C

177605677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53839061-G-A

177605713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53839025-C-T

177605745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838983-G-A

177605746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838982-G-T

177605875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838874-G-A

177605875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838874-G-C

177605909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838840-T-G

177605926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838826-G-A

177607770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838467-A-G

177607771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838466-C-T

177607942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838296-A-G

177608264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838037-T-G

177608282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838021-C-T

177608298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53838005-A-G

177608347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53835793-A-G

177609015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53835470-G-C

177609211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53835279-T-C

http://identifiers.org/hco/4/GRCh38#177609547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53833622-A-C

177609645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53833501-T-G

177609679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53833464-A-G

177609679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53833464-A-T

177609681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53833462-G-A

177610169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53833044-A-G

177610171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53833042-G-A

http://identifiers.org/hco/4/GRCh38#177610330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53832890-A-C

http://identifiers.org/hco/4/GRCh38#177610335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53832885-C-A

177612655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53829947-T-A

http://identifiers.org/hco/4/GRCh38#177612668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53829938-A-C

177612702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53829908-C-T

177612712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53829898-T-C

177613198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53828817-G-A

177613328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53828675-C-T

177613329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53828674-G-A

177613415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53828589-A-G

177613549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53828457-T-C

177613707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53828306-T-C

177614264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53827854-C-T

177614334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53827781-T-C

177614469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53827626-C-T

http://identifiers.org/hco/4/GRCh38#177614594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53827470-C-A

177614995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53827062-A-G

177615359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53826693-A-G

http://identifiers.org/hco/4/GRCh38#177615365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53826687-A-C

177615391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53826661-T-G

177615649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53826405-C-T

177615839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53826206-T-A

177615839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53826206-T-G

177616019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53825611-G-A

177616160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53825487-A-G

177616623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53825098-C-G

177616926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53823380-G-C

177616940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53823374-G-A

177616940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53823374-G-C

177617002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53823308-G-A

177617002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53823308-G-C

http://identifiers.org/hco/4/GRCh38#177617253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53823059-A-C

http://identifiers.org/hco/4/GRCh38#177617448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53822899-A-C

177617718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53822626-T-C

177617803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53822542-G-A

177617827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53822518-T-G

177618352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53822317-G-A

177618352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53822317-G-T

177618387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53822282-G-A

177618482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53822178-G-C

177618529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53822144-A-G

177618814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53821860-A-G

177618880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53821797-G-C

177618927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53821768-T-C

177619160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53821556-A-G

http://identifiers.org/hco/4/GRCh38#177619210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53821510-C-A

177619425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53821322-G-A

177619425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53821322-G-T

177634950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53818852-A-G

177634989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53818813-G-A

177634989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53818813-G-T

177635717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53817323-C-G

177635717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53817323-C-T

http://identifiers.org/hco/4/GRCh38#177635836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53817215-C-A

177635836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53817215-C-T

http://identifiers.org/hco/4/GRCh38#177635898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53817154-C-A

http://identifiers.org/hco/4/GRCh38#177636023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53817029-C-A

177636065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53816991-A-T

177641565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53812964-A-G

177641595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53812934-T-A

177641773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53811683-G-T

177642195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53811257-A-G

177642223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53811227-A-G

177642261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53811190-T-C

177642282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53811169-A-G

177642494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53810958-A-T

http://identifiers.org/hco/4/GRCh38#177642518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53810934-C-A

177642518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53810934-C-G

177642736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53810761-G-A

177642898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53810709-C-G

177642898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53810709-C-T

177642899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53810708-G-A

http://identifiers.org/hco/4/GRCh38#177642976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53810634-C-A

177643064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53810544-T-A

177643099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53810507-C-T

177643181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53810426-A-G

177643181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53810426-A-T

http://identifiers.org/hco/4/GRCh38#177644090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53809504-C-A

177644131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53809462-T-G

177644132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53809461-G-A

177644362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53809254-G-C

http://identifiers.org/hco/4/GRCh38#177645079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53808775-A-C

177645079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53808775-A-G

177645268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53808607-A-G

177645280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53808574-T-C

177645328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53808526-C-G

177645354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53808502-A-G

177645671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53808170-A-G

177645830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53807807-A-G

177645849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53807780-T-C

177645849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53807780-T-G

177645851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53807778-T-C

177645851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53807778-T-G

http://identifiers.org/hco/4/GRCh38#177645880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53807699-C-A

177645910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53807654-T-G

177646639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53806806-A-T

177646970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53806494-G-C

177647009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53806456-A-G

177647156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53806291-T-C

177647171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53806276-A-G

http://identifiers.org/hco/4/GRCh38#177647182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53806265-C-A

http://identifiers.org/hco/4/GRCh38#177647213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53806257-C-A

177647450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53805977-G-A

177647639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53805784-A-G

177647735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53805688-T-A

177648162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53805280-C-G

177648595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53804787-T-C

177648839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53804548-T-G

177648874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53804509-T-G

177648890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53804493-T-C

http://identifiers.org/hco/4/GRCh38#177649062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53803496-A-C

177649415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53803055-T-C

http://identifiers.org/hco/4/GRCh38#177651942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53802404-C-A

177651996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53802348-T-C

177652241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53802104-G-A

177652331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53802015-C-G

177660494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53795521-C-T

177660711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53795282-A-G

177660874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53795116-T-A

http://identifiers.org/hco/4/GRCh38#177675865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53793062-A-C

177675913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53793018-G-T

177675924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53793007-A-G

http://identifiers.org/hco/4/GRCh38#177675925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53793006-A-C

177675925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53793006-A-G

http://identifiers.org/hco/4/GRCh38#177675993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53792928-C-A

177675993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53792928-C-G

http://identifiers.org/hco/4/GRCh38#177675997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53792924-C-A

177675997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53792924-C-T

177676081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53792843-G-A

177676157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53792767-A-G

177676325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53792603-T-C

177676326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53792602-A-G

177676639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53785687-G-A

177676639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53785687-G-T

177676710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53785616-G-T

177676787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53785540-T-A

177677050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53785292-T-C

177677385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53784965-T-C

http://identifiers.org/hco/4/GRCh38#177677415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53784935-A-C

177677453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53784898-G-T

177677561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53784798-A-G

177677620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53784724-G-A

177677620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53784724-G-T

177678558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53784225-T-C

177678570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53784213-C-T

http://identifiers.org/hco/4/GRCh38#177678678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53784106-A-C

177678720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53784061-T-C

177678827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53783975-A-G

177678928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53783920-G-A

177678951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53783897-A-G

http://identifiers.org/hco/4/GRCh38#177679067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53783783-C-A

177679067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53783783-C-T

http://identifiers.org/hco/4/GRCh38#177679170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53783687-A-C

177679170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53783687-A-G

177679327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53783569-T-C

177679351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53783545-A-G

177679383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53783508-A-G

177679405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53783488-A-G

177679416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53783482-G-A

177679689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53783236-T-A

177685358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53781732-G-C

177685647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53781465-T-G

177685701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53781432-A-G

177685945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53781229-C-T

177686455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53777476-A-T

177686527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53777402-T-C

http://identifiers.org/hco/4/GRCh38#177686597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#53777328-C-A