39491792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123236640-G-A

39491792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123236640-G-T

http://identifiers.org/hco/1/GRCh38#39491803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123236632-C-A

39491803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123236632-C-T

39491849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123236609-G-A

39491855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123236603-G-A

39491855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123236603-G-C

39491855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123236603-G-T

39491856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123236602-C-T

http://identifiers.org/hco/1/GRCh38#39491865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123236593-C-A

39491865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123236593-C-T

39491916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123236561-T-C

39491916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123236561-T-G

39491943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123236540-G-T

http://identifiers.org/hco/1/GRCh38#39491986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123236505-C-A

39491986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 123236505-C-T

http://identifiers.org/hco/1/GRCh38#39492070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123236424-C-A

39492070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123236424-C-T

39492260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123236240-A-G

39492295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123236205-G-A

39492295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123236205-G-C

39492295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123236205-G-T

39492367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123236137-G-A

39492367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123236137-G-T

39492388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123236113-T-C

39492388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123236113-T-G

http://identifiers.org/hco/1/GRCh38#39492390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#123236111-C-A

39492390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123236111-C-G

39492390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123236111-C-T

39492484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123236045-G-C

39493019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123235567-C-T

39493145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123234819-C-G

39493145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123234819-C-T

39493344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123234678-C-T

39493483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123234582-G-A

39493526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123234539-T-G

39493639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123234437-G-A

39493765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123234337-C-T

http://identifiers.org/hco/1/GRCh38#39493766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123234336-A-C

39493907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123234195-G-A

39495378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123232909-G-A

39495482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123232836-C-G

39495711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123232600-C-T

39495721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123232590-C-T

39495969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123232401-C-T

39496006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123232364-T-C

39496049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123232318-G-C

39496066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123232301-G-C

39496079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123232288-G-A

39496292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123232041-A-G

39496374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123231891-C-T

39496446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123231802-A-G

http://identifiers.org/hco/1/GRCh38#39496512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123231740-C-A

http://identifiers.org/hco/1/GRCh38#39496748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123231546-C-A

http://identifiers.org/hco/1/GRCh38#39496752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123231540-C-A

39497759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123229875-C-G

http://identifiers.org/hco/1/GRCh38#39498018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123229640-A-C

39498445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123229302-G-A

39498553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123229194-T-G

39498608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123229140-G-A

39498609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123229139-G-T

39498734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123229035-G-A

39498742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123229027-G-A

39498789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228980-C-T

39498809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228961-T-C

39498823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228947-G-A

39498844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228926-A-G

39499036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228762-G-A

39499051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228746-A-G

39499130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228669-G-A

39499162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228640-A-G

39499415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228423-T-G

39499495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228345-A-G

39499599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228237-G-A

39499599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228237-G-T

39499766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123228033-C-G

39507002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123223128-A-G

39507104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123223037-A-G

39507241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222915-C-G

39507474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222766-A-G

39507511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222731-G-A

39507511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222731-G-T

39507617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222580-G-A

39507973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123222286-C-T

39508261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221874-A-G

39508344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221647-C-G

39508344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221647-C-T

39508652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221337-C-T

39508842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221158-C-T

39508877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221127-C-G

39509016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123221017-G-A

39509144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123220964-G-A

39509154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123220954-G-A

http://identifiers.org/hco/1/GRCh38#39509515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123220643-C-A

39509824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123220357-G-A

39510533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123219570-G-T

39510736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123219387-A-T

39510749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123219383-C-T

39510900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123219235-G-A

http://identifiers.org/hco/1/GRCh38#39511053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123219153-C-A

39511176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 123219077-G-T

39511290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123218963-G-T

http://identifiers.org/hco/1/GRCh38#39511413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123218850-C-A

39511413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218850-C-T

39511452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218822-T-A

39511452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218822-T-C

39511452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218822-T-G

39511477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218797-G-A

39511477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218797-G-T

39511492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218792-G-A

39511644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218621-G-A

39511670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218593-A-T

39511763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123218493-G-T

39511823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123218433-G-T

39511871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123218385-C-T

http://identifiers.org/hco/1/GRCh38#39511896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123218360-C-A

39511896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123218360-C-G

39511896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123218360-C-T

39511897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123218359-T-A

39511897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123218359-T-C

39511897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 123218359-T-G

39511908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218348-A-G

39511908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218348-A-T

39511934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218315-G-A

39511934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218315-G-T

39511957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218287-G-T

39512040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218204-G-A

39512052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123218173-G-T

39512335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 123217903-G-C

39512375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 123217866-T-G

39512416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 123217830-C-T

http://identifiers.org/hco/1/GRCh38#39512473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#123217761-C-A

39512603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217629-G-A

http://identifiers.org/hco/1/GRCh38#39514895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#123217466-C-A

39514895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123217466-C-T

39514898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123217463-G-A

39514910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123217451-A-T

39514916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217445-G-A

39514916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217445-G-T

39514928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217432-T-C

39514928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217432-T-G

39514935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123217425-G-T

39514998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123217335-G-A

http://identifiers.org/hco/1/GRCh38#39515015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#123217318-A-C

39515019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123217314-C-T

39515124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217209-G-A

39515124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217209-G-C

39515124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217209-G-T

39515148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217185-G-A

39515148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217185-G-C

39515148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217185-G-T

39515166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217167-G-A

39515166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217167-G-C

39515166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123217167-G-T

39515374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123216959-C-T

39515379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123216954-G-A

39515379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123216954-G-C

39515407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123216926-G-C

39515436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123216897-T-C

39515598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123216735-G-A

39515607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123216726-G-A

39515607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123216726-G-T

39515714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 123216600-C-T

39515867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123216444-G-A

39515867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123216444-G-C

39515867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123216444-G-T

39515886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123216425-A-G

39515886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123216425-A-T

39515978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123216333-G-A

http://identifiers.org/hco/1/GRCh38#39516092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123216219-A-C

http://identifiers.org/hco/1/GRCh38#39516134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123216177-C-A

39516347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215964-G-A

39516347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215964-G-T

39516380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215931-A-T

http://identifiers.org/hco/1/GRCh38#39516392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123215919-C-A

39516392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215919-C-T

http://identifiers.org/hco/1/GRCh38#39516403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123215908-C-A

39516403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215908-C-G

39516403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215908-C-T

39516483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215828-T-A

39516483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215828-T-C

39516483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215828-T-G

http://identifiers.org/hco/1/GRCh38#39516497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123215808-C-A

39516497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215808-C-T

http://identifiers.org/hco/1/GRCh38#39516525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123215787-C-A

http://identifiers.org/hco/1/GRCh38#39516596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123215732-C-A

http://identifiers.org/hco/1/GRCh38#39516597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123215731-C-A

39516597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215731-C-T

39516604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123215724-C-T

http://identifiers.org/hco/1/GRCh38#39516877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123215486-C-A

39518643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123214513-G-T

39518694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123214463-C-T

http://identifiers.org/hco/1/GRCh38#39518783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123214393-C-A

39518783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123214393-C-T

http://identifiers.org/hco/1/GRCh38#39518793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123214390-A-C

39518888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123214296-T-C

39518894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123214290-A-G

39518895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123214289-G-A

39519062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123214083-T-C

39519133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123214037-G-A

39519133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123214037-G-T

39519141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123214028-T-C

39519181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123213987-A-G

39519181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123213987-A-T

39519194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123213974-C-T

39519382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123213803-C-T

39519502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123213726-C-G

39519543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, undefined
orthologous variants: 123213690-G-C

39519579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123213655-G-A

39519579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123213655-G-C

http://identifiers.org/hco/1/GRCh38#39520600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123211727-A-C

39520619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123211708-G-A

39520619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123211708-G-T

39520959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123211367-A-G

http://identifiers.org/hco/1/GRCh38#39521232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123211051-A-C

39521232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, missense_variant
orthologous variants: 123211051-A-G

39521232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, missense_variant
orthologous variants: 123211051-A-T

39521234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, missense_variant
orthologous variants: 123211049-G-C

http://identifiers.org/hco/1/GRCh38#39521290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123210966-C-A

39521290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, missense_variant
orthologous variants: 123210966-C-T

39521423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense variant
orthologous variants: 123210800-C-T

39521477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense variant
orthologous variants: 123210746-A-G

http://identifiers.org/hco/1/GRCh38#39521555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123210668-C-A

39521555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: missense variant
orthologous variants: 123210668-C-T

39522011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210601-T-G

39522113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210515-G-A

http://identifiers.org/hco/1/GRCh38#39522198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123210432-C-A

39522198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210432-C-G

39522198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210432-C-T

39522216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210409-G-A

39522216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210409-G-C

39522216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210409-G-T

39522226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210398-T-A

39522226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210398-T-C

39522227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210397-G-A

39522227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210397-G-T

http://identifiers.org/hco/1/GRCh38#39522242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123210382-A-C

39522242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210382-A-G

39522242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210382-A-T

39522258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210366-G-A

39522258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210366-G-T

http://identifiers.org/hco/1/GRCh38#39522278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123210346-A-C

39522278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron variant
orthologous variants: 123210346-A-G

39522308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 123210315-A-G

39522507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 123210120-T-C

39522507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 123210120-T-G

39522532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123210107-T-A

39522633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123210092-G-T

39522643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123210082-G-C

39522643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123210082-G-T

39522812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209907-C-T

39522919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209817-C-T

39522920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209816-G-A

39522920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209816-G-T

39522931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209800-G-A

39522931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209800-G-T

39522994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209756-C-T

39522995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209755-C-T

39523019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 123209733-G-A

39523152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 123209601-G-C

http://identifiers.org/hco/1/GRCh38#39525585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123207277-C-A

39525585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123207277-C-T

39525593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123207269-G-A

39525606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123207257-G-A

39525627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123207236-C-G

39525627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 123207236-C-T

39525883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123206972-G-A

39525919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 123206934-G-T

39526198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123206649-C-T

http://identifiers.org/hco/1/GRCh38#39527060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123206002-C-A

39527162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123205895-G-A

39527529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123205557-T-C

39527566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123205521-C-T

39529249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123203786-A-G

http://identifiers.org/hco/1/GRCh38#39529261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123203773-C-A

39529261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123203773-C-T

39529277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123203759-G-A

39529301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 123203735-T-C

http://identifiers.org/hco/1/GRCh38#39529654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21650
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#123203419-A-C