3725233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3899369-T-A

3725233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3899369-T-C

3725405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3899521-G-T

3725599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3899702-G-A

3725600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3899703-G-A

3725600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3899703-G-C

3725600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3899703-G-T

3725916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3899994-G-A

3726216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3900233-C-T

3726365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3900389-G-A

http://identifiers.org/hco/16/GRCh38#3727469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3901506-C-A

3727469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: 3901506-C-G

http://identifiers.org/hco/16/GRCh38#3727471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3901508-A-C

3727958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: synonymous variant
orthologous variants: 3902152-C-T

http://identifiers.org/hco/16/GRCh38#3727982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3902176-C-A

3727982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense variant
orthologous variants: 3902176-C-G

3728042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: synonymous variant
orthologous variants: 3902236-G-A

3728042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense variant
orthologous variants: 3902236-G-C

3728042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: synonymous variant
orthologous variants: 3902236-G-T

3728405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense variant
orthologous variants: 3902596-C-G

3728426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: synonymous variant
orthologous variants: 3902617-T-C

3728426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense variant
orthologous variants: 3902617-T-G

3728618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense variant
orthologous variants: 3902806-A-T

3729091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense variant
orthologous variants: 3903279-T-C

3730944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3905303-C-T

3730979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3905352-C-T

3731091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3905447-C-G

3731091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3905447-C-T

http://identifiers.org/hco/16/GRCh38#3731121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3905477-C-A

3731121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3905477-C-T

3731716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3906046-T-C

http://identifiers.org/hco/16/GRCh38#3731751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3906080-C-A

3731751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3906080-C-T

3731752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3906081-T-A

http://identifiers.org/hco/16/GRCh38#3731760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3906091-C-A

3731760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3906091-C-T

3736168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3909788-G-A

http://identifiers.org/hco/16/GRCh38#3736213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3909833-C-A

3736237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3909857-C-G

3736644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3910048-G-A

3736644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3910048-G-C

3736644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3910048-G-T

3736686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3910090-G-T

3736707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3910111-C-T

3736952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3910346-G-A

3736956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3910350-G-A

3736956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3910350-G-T

3737144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3910772-T-C

3737144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3910772-T-G

3737347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3910913-C-T

3738261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3911094-A-G

3738350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3911174-G-T

http://identifiers.org/hco/16/GRCh38#3738648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3911425-A-C

3738689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3911472-C-T

http://identifiers.org/hco/16/GRCh38#3738743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3911531-A-C

3739421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3911855-T-C

3739507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3911973-C-T

3739509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3911975-C-G

3739565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3912025-G-C

3739795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3912248-G-T

3739851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3912289-G-A

3739851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3912289-G-C

3740328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3912445-G-A

3740328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3912445-G-T

3740336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3912452-C-G

3740336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3912452-C-T

3740416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3912517-C-T

3740521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3912622-G-A

3740521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3912622-G-C

3740727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3912788-T-C

3740739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3912798-T-A

3744460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3913741-T-C

3745216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3914246-G-A

3745216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3914246-G-C

3745216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3914246-G-T

http://identifiers.org/hco/16/GRCh38#3745242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3914262-C-A

3745242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3914262-C-G

3745242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3914262-C-T

3745394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3914417-C-G

3745394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3914417-C-T

3745418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3914441-A-G

3745462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3914485-G-A

3745462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3914485-G-T

http://identifiers.org/hco/16/GRCh38#3745499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3914521-C-A

3745499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3914521-C-G

3745618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3914607-T-A

3747286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3915837-T-C

3747336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3915884-T-C

3749544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3917374-T-A

3749608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3917462-G-C

3749615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3917527-C-G

3749615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3917527-C-T

http://identifiers.org/hco/16/GRCh38#3752034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3919729-C-A

3752292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3919974-T-C

3752469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3920143-C-T

3753077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3920764-T-C

3754489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3921988-A-G

3754766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3922254-C-T

3754994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3922473-T-C

3755010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3922488-G-C

3756249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3924217-G-A

3756255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3924225-C-T

3756596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3924569-T-C

http://identifiers.org/hco/16/GRCh38#3757135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3925070-A-C

3757207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3925198-A-G

3757207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3925198-A-T

http://identifiers.org/hco/16/GRCh38#3757463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3925460-A-C

3757780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3925878-T-A

3757780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3925878-T-C

http://identifiers.org/hco/16/GRCh38#3758087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3926175-C-A

3758087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3926175-C-T

http://identifiers.org/hco/16/GRCh38#3758585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3926591-C-A

3758585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3926591-C-T

3758869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense variant
orthologous variants: 3926979-C-G

3758869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: synonymous variant
orthologous variants: 3926979-C-T

3759036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3927132-T-C

3759040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3927136-A-G

3759073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3927169-A-G

3759073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3927169-A-T

3759813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3927610-T-G

3761572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3928358-T-G

http://identifiers.org/hco/16/GRCh38#3761611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3928396-C-A

3761653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3928439-G-A

3761677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3928454-A-T

http://identifiers.org/hco/16/GRCh38#3761699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3928473-C-A

3761699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3928473-C-T

3767219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3932048-G-T

http://identifiers.org/hco/16/GRCh38#3767223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3932052-C-A

3767223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3932052-C-G

3767223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3932052-C-T

3767228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3932054-G-T

3767265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3932101-T-C

3767285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3932124-T-C

3767395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932330-G-A

3767395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932330-G-C

3767471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932389-A-G

3767485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932403-G-A

3767485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932403-G-C

3767485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932403-G-T

http://identifiers.org/hco/16/GRCh38#3767491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3932409-C-A

3767491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932409-C-T

3767524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932438-T-C

http://identifiers.org/hco/16/GRCh38#3767545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3932459-A-C

3767545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932459-A-G

3767590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932526-G-A

3767590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3932526-G-T

http://identifiers.org/hco/16/GRCh38#3767979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3932901-A-C

3768021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3932935-G-T

http://identifiers.org/hco/16/GRCh38#3769077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3933572-A-C

3769249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3933717-C-T

3769353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 3933821-G-C

http://identifiers.org/hco/16/GRCh38#3769389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3933857-A-C

3769492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3933935-G-A

3769492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3933935-G-T

http://identifiers.org/hco/16/GRCh38#3769519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3933959-C-A

3769700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3934130-G-T

http://identifiers.org/hco/16/GRCh38#3770543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3935098-A-C

3770543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3935098-A-G

3770632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3935181-C-T

3770924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 3935470-C-T

3773188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3936373-T-G

3773518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3936689-T-A

3773712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3936858-T-C

3773794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3936940-C-G

3773794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3936940-C-T

3773880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3937035-T-C

3774780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3937801-T-C

3775593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3938415-C-T

3775614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3938436-G-A

3775834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3938650-T-C

3777446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3941880-A-G

3777458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3941891-A-G

3777510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3941939-G-A

3777510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3941939-G-C

3777510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3941939-G-T

3777534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3941954-G-A

3777534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3941954-G-T

3777547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3941967-A-G

3777575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3941996-T-C

http://identifiers.org/hco/16/GRCh38#3777895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3942383-C-A

3777895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3942383-C-T

3777993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3942482-A-G

3777993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3942482-A-T

3778194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3942683-T-C

3778255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3942740-T-C

http://identifiers.org/hco/16/GRCh38#3778445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3943094-A-C

3778567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3943392-G-T

3778573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3943398-T-C

3781287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: synonymous variant
orthologous variants: 3944817-A-G

http://identifiers.org/hco/16/GRCh38#3781415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3944919-A-C

3781415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3944919-A-G

3782141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3945653-C-T

3782361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3945888-G-A

3782414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3946056-G-T

3782571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3946194-A-G

http://identifiers.org/hco/16/GRCh38#3782609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3946232-C-A

3782609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3946232-C-G

3782629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3946254-T-C

3782636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3946261-T-G

3782651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3946276-A-T

3782667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3946291-A-G

3783553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3947144-C-T

3783612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3947172-C-G

3783686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3947253-C-T

3783806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3947359-G-A

http://identifiers.org/hco/16/GRCh38#3785185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3949147-A-C

3785455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3949369-T-A

3785492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3949402-G-A

3789929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3953561-A-G

3789966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3953595-G-A

3790684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3954134-T-C

3790702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3954153-A-G

3790717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3954168-A-G

3791012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3954365-G-A

3791012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3954365-G-T

3791027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3954380-G-A

3791170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3954507-A-G

3791181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3954518-C-T

3791229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3954567-G-A

3791229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3954567-G-T

http://identifiers.org/hco/16/GRCh38#3791332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3954663-C-A

3791332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3954663-C-T

3791387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3954720-A-G

http://identifiers.org/hco/16/GRCh38#3791611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3954879-C-A

3791611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3954879-C-G

http://identifiers.org/hco/16/GRCh38#3791851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3955103-C-A

3791851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3955103-C-T

http://identifiers.org/hco/16/GRCh38#3791858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3955110-C-A

3791858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3955110-C-G

3791886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3955137-A-G

3791958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3955207-T-C

3792356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3955606-A-T

3792837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3956095-G-A

3792963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3956179-C-T

3793132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3956360-C-T

3793183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3956409-C-T

3793219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3956444-C-G

3793252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3956476-A-G

3793274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, undefined
orthologous variants: 3956500-G-A

3793274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, undefined
orthologous variants: 3956500-G-T

3793335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3956559-G-A

3793335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3956559-G-C

3793335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3956559-G-T

3793844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3957047-C-T

3794034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3957239-T-C

3794710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3957546-G-C

3794710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3957546-G-T

http://identifiers.org/hco/16/GRCh38#3794733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3957569-C-A

3805971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3965922-C-G

3806604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3966504-T-C

3806885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3969498-A-G

3807010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3969586-G-A

3807805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3970684-C-G

3808783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3971474-T-C

3808966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3971604-G-C

3809127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3971750-T-C

3809894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3972147-C-T

3810252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3972409-C-G

3810347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3972493-T-G

3810376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3972521-G-C

3810514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, undefined
orthologous variants: 3972634-T-A

3810571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3972689-A-G

http://identifiers.org/hco/16/GRCh38#3810575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3972693-A-C

3810575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3972693-A-G

3810878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3973003-G-T

http://identifiers.org/hco/16/GRCh38#3811041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3973198-C-A

3811041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3973198-C-T

3816220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3974694-T-G

3816884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3975243-G-A

3816884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3975243-G-C

3816920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3975272-G-C

3817167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3975622-G-C

3817550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3976001-T-A

3817825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3976323-C-T

3818135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3976605-A-G

3818803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3976905-T-C

3818803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3976905-T-G

3819006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3977074-C-T

3819088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3977134-C-T

3819780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3978152-A-G

3819799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3978171-G-C

3819866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3978228-C-T

3819867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3978229-G-A

http://identifiers.org/hco/16/GRCh38#3820016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3978371-C-A

3823470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3981559-A-T

3823520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3981616-G-A

3823801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3981872-T-A

3823801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3981872-T-C

3823807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3981878-G-C

3825566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3982292-G-C

3827144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3986219-T-C

3829228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3987383-T-C

3829473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3987586-G-A

http://identifiers.org/hco/16/GRCh38#3829598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3987698-A-C

3829635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3987731-T-C

3830038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3988120-G-A

3841720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3990815-T-C

3841743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3990842-C-T

3843999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3992375-T-C

3844058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3992434-G-T

3844134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3992498-C-T

3844343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3992589-T-C

3844361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3992607-T-C

3844361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3992607-T-G

3844449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3992685-T-C

3844449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3992685-T-G

3844596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3992808-G-C

3844845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3993021-C-T

3849280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3996406-T-C

3849920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3996744-C-T

http://identifiers.org/hco/16/GRCh38#3849942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#3996766-A-C

3851050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3998038-C-G

3851050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3998038-C-T

3851157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3998274-G-A

3851157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3998274-G-T

3851309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3998413-A-T

3851582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3998564-T-C

3851582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3998564-T-G

3852677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3998903-G-C

3852695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3998920-T-C

3852926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3999140-T-C

3854478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 3999382-T-C

http://identifiers.org/hco/16/GRCh38#3856735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4000970-C-A

3856959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4001509-A-G

3857007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4001560-G-A

3857838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4002874-C-G

3857937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4002971-A-G

http://identifiers.org/hco/16/GRCh38#3858727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4004693-C-A

3858963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4004883-T-C

3860263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4005260-C-T

3861749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4006215-G-C

3861783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4006243-T-C

3863636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4007754-C-G

3863743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4007844-G-C

3863830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4007950-G-A

3863995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4008115-T-C

3866640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4010729-T-G

http://identifiers.org/hco/16/GRCh38#3866759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4013396-C-A

3868784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4014880-C-T

http://identifiers.org/hco/16/GRCh38#3868850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4014945-C-A

3870170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4016832-G-A

3870315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4016974-C-G

3870679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4017319-C-T

3871875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4018280-T-C

3872254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4018643-G-C

3872466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4018814-A-T

3872515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4018859-A-T

3872767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4022989-C-G

3873559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4023912-C-G

3873559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4023912-C-T

3873828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4024169-T-C

http://identifiers.org/hco/16/GRCh38#3873855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4024200-C-A

3873855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4024200-C-T

3873991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4024336-T-C

3874018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4024366-G-A

http://identifiers.org/hco/16/GRCh38#3874057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4024397-A-C

3874158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4024500-G-C

http://identifiers.org/hco/16/GRCh38#3874417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4024708-C-A

3874532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4024828-T-G

3874863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4025294-G-A

3874992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4025404-T-A

3876658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4028194-T-C

http://identifiers.org/hco/16/GRCh38#3876698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#4028237-C-A

3876851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4028338-A-G

http://identifiers.org/hco/16/GRCh38#3877391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4029019-C-A

3878204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4029641-G-A

3878233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4029670-C-G

3878239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4029680-A-G

3878250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4029691-G-A

3878250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4029691-G-C

3878498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4029938-A-G

3878505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4029945-T-C

3879272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: 4030644-G-C

http://identifiers.org/hco/16/GRCh38#3879822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#4030993-C-A

3880010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5 prime UTR variant
orthologous variants: 4031171-G-A

3880010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5 prime UTR variant
orthologous variants: 4031171-G-T

3880320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5 prime UTR variant
orthologous variants: 4031479-T-C

3880320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5 prime UTR variant
orthologous variants: 4031479-T-G

3880333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5 prime UTR variant
orthologous variants: 4031492-G-A

3880333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5 prime UTR variant
orthologous variants: 4031492-G-C

3880333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5 prime UTR variant
orthologous variants: 4031492-G-T

3880402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5 prime UTR variant
orthologous variants: 4031563-G-A

3880402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5 prime UTR variant
orthologous variants: 4031563-G-C

3880402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5 prime UTR variant
orthologous variants: 4031563-G-T

http://identifiers.org/hco/16/GRCh38#3880694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2348
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#4031834-C-A