95237669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210779-G-A

95237669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210779-G-C

95237669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210779-G-T

http://identifiers.org/hco/10/GRCh38#95237693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40210804-C-A

95237693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210804-C-T

95237741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210850-G-A

95237741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210850-G-T

http://identifiers.org/hco/10/GRCh38#95237752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40210861-C-A

95237752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210861-C-T

http://identifiers.org/hco/10/GRCh38#95237758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40210867-A-C

http://identifiers.org/hco/10/GRCh38#95237781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40210890-C-A

95237793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210896-G-C

95237793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210896-G-T

95237838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210940-G-A

95237838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210940-G-T

95237879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210980-A-G

95237895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 3 prime UTR variant
orthologous variants: 40210994-T-C

http://identifiers.org/hco/10/GRCh38#95237952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/19/GRCm39#40211056-A-C

95237952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40211056-A-G

95237967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40211071-T-C

95237974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40211078-C-G

95237974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40211078-C-T

95237981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40211085-G-A

95237984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40211088-C-T

95238000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40211104-G-A

95238095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40211199-G-C

http://identifiers.org/hco/10/GRCh38#95238115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40211219-C-A

95238115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 40211219-C-T

95238123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211226-A-G

http://identifiers.org/hco/10/GRCh38#95238172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40211258-A-C

95238172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211258-A-G

http://identifiers.org/hco/10/GRCh38#95238187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40211271-C-A

95238202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211286-G-A

95238202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211286-G-T

95238461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211399-G-A

95238461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211399-G-T

95238464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211402-T-C

95238488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211426-G-A

95238488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211426-G-T

95238509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40211447-A-G

95238573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40211500-C-T

95238586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40211513-T-A

95238642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40211569-A-G

http://identifiers.org/hco/10/GRCh38#95238681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40211608-A-C

95238730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40211659-G-A

95238730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40211659-G-C

95238730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40211659-G-T

95238756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40211686-A-G

95238756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40211686-A-T

95238788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40211723-T-C

95238816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40211741-T-C

95241925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40212314-G-A

95241933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40212322-G-A

95241933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40212322-G-C

95242028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40212419-C-G

95242028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40212419-C-T

95242052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40212439-G-A

http://identifiers.org/hco/10/GRCh38#95242236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40212570-A-C

95242760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40213687-G-A

95242944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40213844-C-T

95243231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40214079-G-C

95243239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40214087-C-G

http://identifiers.org/hco/10/GRCh38#95243263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40214111-C-A

95243263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214111-C-T

95243521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214336-C-T

95243545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214360-G-A

95243602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214412-A-G

95243746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214556-T-A

95243746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214556-T-C

95243758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214568-G-A

95243758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40214568-G-T

95245221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40215748-T-C

95245344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40215867-A-G

95245363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40215878-C-T

95245475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40215989-G-A

95245502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40216025-C-T

95245623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40216147-T-C

95245648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40216172-C-T

95246148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40216453-G-A

95246331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40216608-G-A

95246569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40216785-G-A

95246791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217172-A-G

95246834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40217202-G-A

95246849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217212-G-A

http://identifiers.org/hco/10/GRCh38#95246921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40217261-C-A

95246921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217261-C-T

95246933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217272-T-A

95246937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40217276-G-A

http://identifiers.org/hco/10/GRCh38#95247106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40218867-C-A

95247106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40218867-C-T

http://identifiers.org/hco/10/GRCh38#95247279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#40219015-A-C

95247279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 40219015-A-G

95247345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 40219081-T-C

95247354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 40219090-A-G

95247388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 40219124-T-C

http://identifiers.org/hco/10/GRCh38#95247437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#40219177-C-A

95247537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40219256-T-C

95247549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40219268-G-A

95247549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40219268-G-C

95247549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40219268-G-T

95247632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219350-G-A

95247632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219350-G-T

http://identifiers.org/hco/10/GRCh38#95247652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40219370-C-A

95247692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219410-T-A

95247718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219436-A-G

95247763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219483-A-T

95247870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219585-G-A

95247962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219674-T-C

95248022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219734-G-A

http://identifiers.org/hco/10/GRCh38#95248126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40219871-A-C

95248203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40219939-T-C

95248994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220374-C-G

95249129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220497-C-T

95249151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220508-C-G

95249177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220530-T-G

http://identifiers.org/hco/10/GRCh38#95249189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40220532-C-A

95249302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220619-G-A

95249398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220734-A-G

95249414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220750-T-A

95249414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220750-T-G

95249436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40220771-T-G

95249957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40221255-G-C

95250227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40221507-T-C

95250557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40221949-A-G

95259624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228135-G-T

95259745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228258-T-A

95259745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228258-T-C

95259755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228268-T-C

95259825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228333-A-G

95259829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228337-A-G

http://identifiers.org/hco/10/GRCh38#95259900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40228409-A-C

http://identifiers.org/hco/10/GRCh38#95259981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40228498-A-C

95260156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228640-T-C

95260217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228701-G-A

95260312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228786-C-G

http://identifiers.org/hco/10/GRCh38#95260505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40228965-A-C

95260536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40228996-C-T

95260579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40229036-C-G

95260585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40229042-C-T

95260636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40229096-G-A

http://identifiers.org/hco/10/GRCh38#95260668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#40229311-A-C

95260735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40229405-A-G

95260774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40229444-A-G

95260777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40229447-T-C

95260854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40229516-C-T

95260856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40229518-G-C

http://identifiers.org/hco/10/GRCh38#95260864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#40229526-C-A

95260934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40229587-T-C

95261015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40229669-G-A

http://identifiers.org/hco/10/GRCh38#95261083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40229736-C-A

95261083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40229736-C-T

95261567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230202-G-A

95262268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230574-T-C

95263163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230921-C-G

95263163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40230921-C-T

95263322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40231041-G-T

http://identifiers.org/hco/10/GRCh38#95263374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#40231089-A-C

95263405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40231120-A-G

95263854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40231838-G-A

http://identifiers.org/hco/10/GRCh38#95263856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40231840-C-A

http://identifiers.org/hco/10/GRCh38#95263875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40231861-C-A

95263875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40231861-C-G

95263875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 40231861-C-T

http://identifiers.org/hco/10/GRCh38#95263899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40231885-C-A

95264080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232060-G-A

http://identifiers.org/hco/10/GRCh38#95264159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40232126-C-A

95264159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232126-C-T

95264166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232135-G-A

95264166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232135-G-C

95264166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232135-G-T

95264224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40232204-C-T

95264516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232453-G-A

95264530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232467-C-T

95264613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232525-G-A

http://identifiers.org/hco/10/GRCh38#95264652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40232571-A-C

95264675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232585-G-C

95264699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232598-G-A

95264699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232598-G-C

95264855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40232713-A-G

95265002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40234275-G-A

95265046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40234316-A-G

95265269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40234511-G-T

95266804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40235816-T-C

95267097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236109-T-C

95267355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236313-T-A

95267513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236464-T-G

95267656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236601-T-C

95267702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236647-C-G

95267702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236647-C-T

95267849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236792-T-C

95267887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40236828-G-C

95267965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237314-C-T

95268178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237494-T-C

95268196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237512-G-C

http://identifiers.org/hco/10/GRCh38#95268203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40237519-A-C

95268453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237729-C-G

95268453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237729-C-T

http://identifiers.org/hco/10/GRCh38#95268455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40237731-A-C

95268455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237731-A-G

95268571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237845-C-T

95268612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40237889-A-G

95268712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40238002-G-A

95268712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40238002-G-C

http://identifiers.org/hco/10/GRCh38#95268917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40238645-C-A

http://identifiers.org/hco/10/GRCh38#95268927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40238655-A-C

95268929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40238657-T-C

http://identifiers.org/hco/10/GRCh38#95268960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40238691-C-A

95268960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40238691-C-T

http://identifiers.org/hco/10/GRCh38#95268973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40238704-C-A

95268973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40238704-C-T

http://identifiers.org/hco/10/GRCh38#95268990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40238721-C-A

95268990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40238721-C-T

95268997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40238728-T-C

95270102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40239386-C-T

95270123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40239411-A-G

95270588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40239881-G-A

95270619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40239912-C-T

http://identifiers.org/hco/10/GRCh38#95270653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40239946-C-A

95271492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240201-A-G

95271492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240201-A-T

http://identifiers.org/hco/10/GRCh38#95271493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40240202-C-A

95271493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240202-C-G

95271493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240202-C-T

95271567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240289-G-A

95271567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240289-G-T

95271623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240344-T-C

95271803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240524-G-A

http://identifiers.org/hco/10/GRCh38#95271829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40240554-A-C

http://identifiers.org/hco/10/GRCh38#95271830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40240555-C-A

95271830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240555-C-T

http://identifiers.org/hco/10/GRCh38#95271860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40240588-C-A

95271862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240590-G-A

95271862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240590-G-T

95271875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40240603-G-T

http://identifiers.org/hco/10/GRCh38#95272264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40241420-C-A

95272280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40241436-A-G

95272290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40241449-A-G

http://identifiers.org/hco/10/GRCh38#95272731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40241555-A-C

95272731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40241555-A-G

http://identifiers.org/hco/10/GRCh38#95273240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40242017-C-A

95273240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40242017-C-G

95273265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40242040-C-T

95273330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40242090-C-T

95273399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40242147-C-T

95273410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242157-G-A

95273410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242157-G-T

95273439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242211-G-A

95273439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242211-G-T

http://identifiers.org/hco/10/GRCh38#95273470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40242243-A-C

95273526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40242296-G-A

95273526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40242296-G-T

http://identifiers.org/hco/10/GRCh38#95273554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40242326-C-A

95273556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242328-C-T

95273589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242358-C-T

95273724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242446-C-G

95273795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242504-T-C

95273795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242504-T-G

95273877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242553-A-T

95274004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242773-A-G

95274018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242787-C-T

95274026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40242795-T-A

95275545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244054-T-G

95275659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244130-T-G

95275835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244278-G-A

95276001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244403-C-T

95276150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244682-G-A

95276185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244799-A-G

95276275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40244891-G-A

95276618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40245186-T-C

http://identifiers.org/hco/10/GRCh38#95278028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40246118-C-A

http://identifiers.org/hco/10/GRCh38#95278290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40246352-A-C

95278486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40246504-T-C

95278514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40246532-G-T

95278635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40246899-A-T

95278666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40246930-G-A

95278739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40247020-T-C

95280669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248667-G-A

95280727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248754-A-G

95280740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248760-A-G

95280888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248902-T-C

http://identifiers.org/hco/10/GRCh38#95280918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40248932-C-A

95280918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40248932-C-G

95281043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40249150-T-C

95281098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40249201-A-T

95281224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40249305-C-T

95281260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40249343-A-G

95281261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40249344-T-C

95281964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40249665-T-C

95282118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40249813-A-G

95282437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40250081-G-T

95282550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40250178-C-T

95282553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40250181-G-A

95283047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40250362-T-C

95283430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40251335-T-C

95283668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40251566-T-C

95284743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40252627-A-T

95285149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253349-C-G

95285149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253349-C-T

http://identifiers.org/hco/10/GRCh38#95285217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40253405-A-C

95285338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253527-G-A

95285338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253527-G-T

95285451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253639-T-C

95285549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40253706-C-T

95286525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40254653-C-T

http://identifiers.org/hco/10/GRCh38#95287180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40255676-A-C

95287206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40255703-G-C

95287808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40256460-T-C

95288248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40256887-A-G

95288390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40257033-T-A

95288390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40257033-T-C

95288938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40257519-G-A

95289431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40258400-T-C

95289496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40258463-G-A

95289794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40258781-A-T

95290005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259042-G-A

95290038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259076-T-C

95290275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259259-G-A

95290316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259300-T-C

95290342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40259335-G-C

95290476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259469-C-T

95290626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259610-G-A

95290686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259652-G-A

95290686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259652-G-C

95290686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259652-G-T

http://identifiers.org/hco/10/GRCh38#95290687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#40259653-C-A

95290750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259721-G-A

95290750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40259721-G-T

95290862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 40259832-G-A

95290862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 40259832-G-T

95290947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40259906-G-A

95290947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40259906-G-C

95290947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40259906-G-T

95290954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40259913-G-A

95290954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40259913-G-T

95290956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40259915-G-A

95290956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40259915-G-C

95290956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2067
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 40259915-G-T