99816842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 137687279-T-C

99816873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137687244-G-A

99816873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 137687244-G-T

99816884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 137687234-T-A

99816910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 137687182-G-A

99816910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 137687182-G-T

http://identifiers.org/hco/4/GRCh38#99816911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137687181-C-A

99816911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 137687181-C-T

99816980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 137687112-T-A

99816980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 137687112-T-G

99817035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137687063-T-A

99817035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137687063-T-C

99817035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137687063-T-G

99817105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137687002-G-C

99817105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137687002-G-T

http://identifiers.org/hco/4/GRCh38#99817117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137686990-C-A

99817117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137686990-C-G

99817163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137686949-A-G

http://identifiers.org/hco/4/GRCh38#99817629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137686532-A-C

99817737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137686426-T-C

99817799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137686390-C-T

99817922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137686274-T-G

99817934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137686262-T-C

99818110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137685912-T-C

99818332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137685725-C-G

99818332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137685725-C-T

http://identifiers.org/hco/4/GRCh38#99818675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137685440-C-A

99818818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137685298-G-T

99818925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137684754-A-G

99819030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137684653-G-A

99819547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137684191-T-C

99819796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137683886-G-A

99819928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137683751-G-A

99819928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137683751-G-C

99820995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137681961-C-T

http://identifiers.org/hco/4/GRCh38#99821105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137681862-A-C

http://identifiers.org/hco/4/GRCh38#99821187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137681780-C-A

99821187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137681780-C-G

99821226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137681742-A-G

99821420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137681550-T-C

99821455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137681526-T-A

99821471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137681510-T-C

99821540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137681442-T-C

http://identifiers.org/hco/4/GRCh38#99821741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137681306-A-C

99821849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137681187-G-A

99822023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137680979-C-T

99822079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137680920-G-A

99822143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137680858-C-T

99822265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137680739-C-T

http://identifiers.org/hco/4/GRCh38#99822464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137680635-A-C

http://identifiers.org/hco/4/GRCh38#99822802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137680363-C-A

http://identifiers.org/hco/4/GRCh38#99822816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137680355-A-C

99823092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137680105-T-C

99823606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137679501-G-A

99823703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137679399-T-C

99823703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137679399-T-G

http://identifiers.org/hco/4/GRCh38#99824207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137678913-A-C

99824463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137678708-G-C

99824476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137678691-G-A

99824706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137678522-T-C

99824779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137678450-T-A

99824966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137678292-T-A

99824966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137678292-T-C

99825099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137678176-C-T

99825145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137678124-G-A

99825151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137678104-A-G

99825190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137678039-T-C

99825200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677996-G-A

99825314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677747-C-T

99825507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677136-C-T

99825918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676802-T-C

http://identifiers.org/hco/4/GRCh38#99825989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137676723-A-C

http://identifiers.org/hco/4/GRCh38#99826019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137676695-C-A

99826147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676562-A-G

99826479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676324-A-G

99826543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676272-A-G

http://identifiers.org/hco/4/GRCh38#99826635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137676079-C-A

99826725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676001-A-G

99827088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137675685-A-G

99827089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137675684-C-T

99828703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137675117-G-C

99835554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137671826-G-A

http://identifiers.org/hco/4/GRCh38#99835576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137671809-C-A

99835576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137671809-C-G

99835576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137671809-C-T

http://identifiers.org/hco/4/GRCh38#99835580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137671805-C-A

99835751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137671635-G-A

99835751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137671635-G-C

99835751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137671635-G-T

http://identifiers.org/hco/4/GRCh38#99835878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137671509-C-A

99837110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137669309-G-C

99837142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137669286-T-A

99837190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137669239-T-C

99838142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137668575-G-A

99838292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137668435-A-T

99838781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137668276-A-G

99839523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667722-G-A

99839597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667655-G-C

99839613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667639-G-A

99839613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667639-G-T

99839838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667540-G-T

99840156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667458-A-G

http://identifiers.org/hco/4/GRCh38#99840210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137667404-C-A

99840210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667404-C-T

http://identifiers.org/hco/4/GRCh38#99840239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137667377-C-A

99840239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667377-C-T

99841126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665627-T-C

99841367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665412-A-G

99841416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665373-C-T

99841476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665320-C-T

99841482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665314-C-T

99841557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665244-G-A

http://identifiers.org/hco/4/GRCh38#99841558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137665243-C-A

99842010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664440-C-T

99842030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664420-A-G

99842097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664362-A-G

http://identifiers.org/hco/4/GRCh38#99842121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137664338-C-A

99842121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664338-C-G

99842241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664155-C-G

http://identifiers.org/hco/4/GRCh38#99842328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137664010-C-A

99842443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137663907-A-G

99842926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137663481-A-G

99842952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137663449-C-T

99843039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137663379-C-T

99843095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137663325-G-A

99843095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137663325-G-C

99843096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137663324-C-T

99843123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137663302-G-C

99843189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137663030-T-A

99843246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662971-G-C

99843528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662709-T-C

99843615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662630-A-T

http://identifiers.org/hco/4/GRCh38#99843873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137662385-C-A

99843873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662385-C-G

99843873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662385-C-T

99843980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662294-G-A

99844353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137662167-A-G

99844532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137662072-T-C

99844794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137661799-T-G

http://identifiers.org/hco/4/GRCh38#99844829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137661765-C-A

99845273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137661294-T-C

http://identifiers.org/hco/4/GRCh38#99845804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137660893-A-C

99845842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137660858-C-T

99845960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137660753-T-C

99846176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137660566-A-G

99846194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137660548-A-T

99846269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137660475-A-G

99846618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137660132-G-C

99846746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137660039-T-C

http://identifiers.org/hco/4/GRCh38#99846924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137659882-C-A

99846924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137659882-C-T

99847051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137659759-G-A

99847051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137659759-G-C

http://identifiers.org/hco/4/GRCh38#99847622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137659074-A-C

99850964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137658015-G-A

99851123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137657816-C-T

99851205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137657752-C-T

99851237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137657722-A-G

99851466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137657476-C-T

99851471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137657471-T-A

99851986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137657048-G-A

http://identifiers.org/hco/4/GRCh38#99851987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137657047-C-A

99851987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137657047-C-T

99852176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137656735-T-G

99852624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137656212-T-C

99852656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137656186-A-G

99852739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137656114-G-A

99852938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655960-C-T

99853018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655908-C-T

99853063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655863-A-G

99853078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655848-T-C

99853087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655836-G-A

99853087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655836-G-T

99853198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655573-T-C

99853322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137655432-G-A

99853340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137655414-G-A

99853421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655353-G-C

99853421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655353-G-T

99853689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137654982-T-C

99853700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137654971-T-C

99853985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137654727-A-G

99854126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137654591-T-A

99854126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137654591-T-G

99855602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137652706-G-A

99856113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137652252-G-T

99856364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137652013-G-A

99857543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137651422-C-T

99858093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137650846-A-T

99858218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137650760-A-G

http://identifiers.org/hco/4/GRCh38#99858270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137650713-C-A

99858349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137650634-A-G

99858391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137650595-C-T

99858706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137650326-A-G

99859428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137649889-A-G

99859446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137649877-A-G

99859568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137649726-T-C

99859590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137649705-G-C

99860376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137649007-A-G

99860987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137647840-T-A

99860987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137647840-T-G

99861126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137647695-C-T

http://identifiers.org/hco/4/GRCh38#99861560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137646685-A-C

99861560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137646685-A-G

99862000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137646002-A-T

99862443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645465-G-C

99862610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645249-T-C

99862703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645161-C-T

http://identifiers.org/hco/4/GRCh38#99862962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137644980-C-A

http://identifiers.org/hco/4/GRCh38#99863005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137644963-C-A

99863331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644459-T-C

http://identifiers.org/hco/4/GRCh38#99863336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137644454-C-A

http://identifiers.org/hco/4/GRCh38#99863631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137643691-A-C

http://identifiers.org/hco/4/GRCh38#99863669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137643659-C-A

99863669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137643659-C-T

99863670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137643658-A-G

99863670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137643658-A-T

http://identifiers.org/hco/4/GRCh38#99863671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137643657-C-A

99863685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137643643-T-G

99863714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137643622-G-T

99863726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137643610-T-C

99863726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137643610-T-G

http://identifiers.org/hco/4/GRCh38#99864007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137643340-C-A

http://identifiers.org/hco/4/GRCh38#99864012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#137643335-C-A

99864012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 137643335-C-T

99864021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137643326-T-A

99864045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137643302-G-A

99864045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137643302-G-T

99864070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137643277-T-C

99864070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137643277-T-G

99864092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137643225-A-T

http://identifiers.org/hco/4/GRCh38#99864235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137643078-C-A

99864235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137643078-C-G

99864247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137643066-G-A

99864247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137643066-G-T

99864288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137643016-G-A

99864288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137643016-G-C

99864330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642974-A-G

99864433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642868-C-T

99864499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642817-C-T

99864583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642737-G-A

99864735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642597-T-C

99864737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642595-G-A

99864737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642595-G-T

http://identifiers.org/hco/4/GRCh38#99864758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137642575-C-A

http://identifiers.org/hco/4/GRCh38#99865032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137642330-C-A

99865034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137642328-A-G

99865066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137642285-G-A

http://identifiers.org/hco/4/GRCh38#99865218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137642193-C-A

99865218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137642193-C-T

http://identifiers.org/hco/4/GRCh38#99865349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137641994-C-A

99865706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137641664-T-A

99865894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137641479-T-A

http://identifiers.org/hco/4/GRCh38#99865895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137641478-C-A

99865895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137641478-C-T

http://identifiers.org/hco/4/GRCh38#99865990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137641463-C-A

99865990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137641463-C-G

99865990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137641463-C-T

http://identifiers.org/hco/4/GRCh38#99866015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137641447-C-A

99866015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137641447-C-G

99866015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137641447-C-T

99866129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137641334-T-A

99866129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137641334-T-C

99866136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641327-G-A

99866136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641327-G-T

99866151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641309-G-A

99866151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641309-G-C

99866151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641309-G-T

http://identifiers.org/hco/4/GRCh38#99866165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137641295-C-A

99866165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641295-C-T

99866177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641286-T-A

99866177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641286-T-C

99866235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641231-G-A

99866235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641231-G-T

http://identifiers.org/hco/4/GRCh38#99866424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137641065-C-A

99866424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641065-C-T

99866523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137640974-G-T

99867738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137639285-C-T

99867986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137639069-G-A

99867986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137639069-G-T

http://identifiers.org/hco/4/GRCh38#99868026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137639031-C-A

99868026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137639031-C-T

99868084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137638977-A-G

http://identifiers.org/hco/4/GRCh38#99868250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137638835-C-A

99868250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137638835-C-G

http://identifiers.org/hco/4/GRCh38#99868334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137638751-C-A

http://identifiers.org/hco/4/GRCh38#99868516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137638588-C-A

99868516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137638588-C-T

99868587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137638519-G-A

99868587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137638519-G-T

http://identifiers.org/hco/4/GRCh38#99869077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137637813-A-C

http://identifiers.org/hco/4/GRCh38#99869127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#137637765-C-A

99869234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137637689-A-T

99869541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137637068-T-C

99870105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16500
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137636807-T-G