50184380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843599-A-G

50184382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843597-G-A

50184382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843597-G-T

50184408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843579-T-C

50184414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843572-C-T

50184415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843571-G-A

http://identifiers.org/hco/17/GRCh38#50184424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94843562-C-A

50184464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843522-G-A

50184464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843522-G-C

50184464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843522-G-T

http://identifiers.org/hco/17/GRCh38#50184470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94843502-A-C

50184470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843502-A-G

50184560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843381-T-C

50184560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843381-T-G

50184653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843289-T-A

http://identifiers.org/hco/17/GRCh38#50184683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94843259-C-A

50184683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843259-C-T

50184860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843107-G-A

50184860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843107-G-T

50184884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843082-T-C

http://identifiers.org/hco/17/GRCh38#50184891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94843057-C-A

50184891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94843057-C-T

50185081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94842869-T-A

50185081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94842869-T-C

50185139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94842810-G-T

50185390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94842557-T-A

50185390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 3 prime UTR variant
orthologous variants: 94842557-T-C

50185505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: synonymous variant
orthologous variants: 94842440-C-T

http://identifiers.org/hco/17/GRCh38#50185506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94842439-A-C

50185506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense variant
orthologous variants: 94842439-A-G

50185529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: synonymous variant
orthologous variants: 94842416-G-A

50185529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense variant
orthologous variants: 94842416-G-C

50185529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense variant
orthologous variants: 94842416-G-T

http://identifiers.org/hco/17/GRCh38#50185530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94842415-A-C

50185566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense variant
orthologous variants: 94842379-G-A

50185670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94842276-G-A

50185670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94842276-G-C

50185726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94842209-A-G

50185761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94842176-G-A

50185848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94842097-G-A

50185994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94841951-G-T

50186266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94841775-C-T

50186316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 94841724-C-G

50186316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 94841724-C-T

50186355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94841685-G-A

50186372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94841668-T-C

50186405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94841635-C-G

50186405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94841635-C-T

http://identifiers.org/hco/17/GRCh38#50186435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94841605-C-A

http://identifiers.org/hco/17/GRCh38#50186451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94841589-A-C

50186486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94841554-T-C

50186611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841429-G-A

50186611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841429-G-T

50186621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841419-G-A

50186621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94841419-G-T

50186786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94841251-A-G

50186786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94841251-A-T

50186822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94841215-T-C

50187003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94841040-G-A

50187003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94841040-G-C

http://identifiers.org/hco/17/GRCh38#50187085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94840958-C-A

50187203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94840834-C-T

http://identifiers.org/hco/17/GRCh38#50187213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94840824-C-A

50187260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94840793-A-T

http://identifiers.org/hco/17/GRCh38#50187831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94840353-C-A

50187831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94840353-C-G

http://identifiers.org/hco/17/GRCh38#50188023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94840134-C-A

50188178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94839978-T-A

50188178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94839978-T-G

http://identifiers.org/hco/17/GRCh38#50188204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94839951-C-A

50188204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94839951-C-G

50188204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94839951-C-T

http://identifiers.org/hco/17/GRCh38#50188273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94839882-C-A

50188339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94839804-G-A

50188339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94839804-G-T

http://identifiers.org/hco/17/GRCh38#50188427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94839723-C-A

50188427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94839723-C-G

50188477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94839673-C-T

50188612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94839555-G-T

http://identifiers.org/hco/17/GRCh38#50188672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94839494-C-A

50188672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94839494-C-G

50188672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94839494-C-T

50188797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: undefined
orthologous variants: 94839365-T-A

50188797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: undefined
orthologous variants: 94839365-T-G

50188862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94839302-C-T

50188887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94839279-G-A

50188887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94839279-G-T

50188985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense variant
orthologous variants: 94839181-G-C

50189232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant
orthologous variants: 94838750-C-T

50189297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94838685-G-A

50189346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94838634-C-T

50189396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant
orthologous variants: 94838584-G-T

50189417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant
orthologous variants: 94838563-G-A

50189553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94838427-G-A

50189553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94838427-G-C

50189557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94838423-G-C

50189618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94838360-T-G

50189988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94838018-C-T

50190008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense variant
orthologous variants: 94837998-C-G

50190008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense variant
orthologous variants: 94837998-C-T

50190083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense variant
orthologous variants: 94837923-T-G

50190131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94837876-G-T

50190150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94837844-G-A

http://identifiers.org/hco/17/GRCh38#50190188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94837797-C-A

50190188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94837797-C-T

50190243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94837745-G-A

50190243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94837745-G-T

50190268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94837720-T-C

http://identifiers.org/hco/17/GRCh38#50190334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94837646-C-A

50190334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94837646-C-G

50190334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94837646-C-T

50190447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94837537-G-A

50190458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94837526-G-C

50190468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94837516-C-T

50190474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94837510-G-C

50190780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94837242-T-A

50190780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94837242-T-C

50190795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94837227-G-A

50190989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94837018-T-C

50190991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94837016-G-C

50190991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94837016-G-T

50191015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836999-T-A

50191049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836982-G-T

50191396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94836729-G-A

50191441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94836684-A-G

50191450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94836675-G-A

http://identifiers.org/hco/17/GRCh38#50191584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94836556-C-A

http://identifiers.org/hco/17/GRCh38#50191628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94836518-C-A

50191628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836518-C-G

50191628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836518-C-T

http://identifiers.org/hco/17/GRCh38#50191776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94836434-C-A

50191776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836434-C-T

50191846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94836364-G-A

50191846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94836364-G-T

50191891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94836319-A-G

50191893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94836317-G-A

http://identifiers.org/hco/17/GRCh38#50191943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94836274-C-A

50191943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836274-C-G

50191943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836274-C-T

http://identifiers.org/hco/17/GRCh38#50191947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94836270-C-A

50191947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94836270-C-T

http://identifiers.org/hco/17/GRCh38#50192135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94836084-C-A

50192135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94836084-C-G

50192135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94836084-C-T

http://identifiers.org/hco/17/GRCh38#50192149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94836070-A-C

50192149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94836070-A-G

http://identifiers.org/hco/17/GRCh38#50192208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94836061-C-A

50192208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94836061-C-G

50192353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94835922-G-A

50192353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94835922-G-T

http://identifiers.org/hco/17/GRCh38#50192360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94835914-C-A

50192545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835720-G-C

50192593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835671-G-C

50192760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835512-T-G

50192875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835380-C-G

50192875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835380-C-T

50192877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835378-C-T

50193013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94835213-G-A

50193084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835143-G-A

50193084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94835143-G-T

50193373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834856-G-C

50193845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94834718-G-A

50193845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94834718-G-C

50193845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94834718-G-T

50193907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94834691-T-A

50193918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94834680-T-G

50193992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94834606-G-C

50193998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94834600-G-C

50194006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94834592-T-A

50194167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94834430-G-A

50194236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834341-G-A

50194236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834341-G-T

50194239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834338-G-A

50194253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834330-G-A

50194253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834330-G-C

50194458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834155-G-A

50194458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834155-G-T

50194467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94834146-G-A

50194619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94833837-G-A

50194619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94833837-G-T

50194694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833758-C-G

50194694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833758-C-T

http://identifiers.org/hco/17/GRCh38#50194742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94833705-C-A

50194742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94833705-C-T

50195004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833470-G-A

50195004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833470-G-T

50195008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833466-G-A

50195008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833466-G-T

50195012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833462-G-A

50195012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833462-G-C

50195012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833462-G-T

50195195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833301-T-C

50195217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833279-G-A

50195259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94833237-G-A

50195259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94833237-G-C

50195424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833082-G-A

50195500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833006-G-A

50195500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94833006-G-T

50195558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94832947-G-A

50195558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94832947-G-T

50195640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94832865-C-T

50195812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94832706-A-T

50195911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94832617-G-A

50195911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94832617-G-C

50195911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94832617-G-T

50195979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 94832549-G-A

50195979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 94832549-G-T

50196075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94832486-T-C

50196159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94832411-G-A

50196285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94832286-G-T

50196374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 94832197-A-G

http://identifiers.org/hco/17/GRCh38#50196537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94832053-C-A

50196600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831996-T-C

50196680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831914-G-A

50196701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831892-C-T

50196708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831885-A-G

50196877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831719-A-G

http://identifiers.org/hco/17/GRCh38#50196880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94831716-C-A

50196880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831716-C-G

50196880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831716-C-T

http://identifiers.org/hco/17/GRCh38#50196882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94831714-C-A

50196882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831714-C-G

50196882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831714-C-T

50196906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831690-G-A

50196906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831690-G-T

50196912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831684-C-T

50196939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831657-G-C

50196939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831657-G-T

50197489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831200-C-T

50197595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831108-A-G

50197595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831108-A-T

50197600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831103-A-G

50197627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831098-T-C

50197627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831098-T-G

50197727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94831000-C-T

50197899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94830826-G-C

50197941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94830791-G-A

50197947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 94830783-A-T

50198012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94830718-A-G

50198137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94830588-T-C

50198353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94830372-G-A

50198353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94830372-G-T

http://identifiers.org/hco/17/GRCh38#50198595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94830116-C-A

http://identifiers.org/hco/17/GRCh38#50198661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94830045-A-C

50198661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94830045-A-G

50198661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94830045-A-T

50198703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, undefined
orthologous variants: 94830003-A-G

http://identifiers.org/hco/17/GRCh38#50198750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94829940-A-C

http://identifiers.org/hco/17/GRCh38#50198804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94829884-A-C

50198804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94829884-A-G

50198838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94829863-T-C

50198838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94829863-T-G

50199091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94829595-T-C

50199182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron variant
orthologous variants: 94829506-A-G

http://identifiers.org/hco/17/GRCh38#50199399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94829260-C-A

50199528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94829109-G-A

50199663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828981-C-T

50199678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828964-C-T

http://identifiers.org/hco/17/GRCh38#50199691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94828951-C-A

50199691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94828951-C-T

50199800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94828881-G-A

50199800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94828881-G-C

50199800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94828881-G-T

http://identifiers.org/hco/17/GRCh38#50199801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94828880-C-A

50199801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94828880-C-T

http://identifiers.org/hco/17/GRCh38#50199874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94828807-C-A

50199874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 94828807-C-T

50200035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94828624-G-C

50200035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94828624-G-T

http://identifiers.org/hco/17/GRCh38#50200053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94828604-C-A

50200053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94828604-C-T

http://identifiers.org/hco/17/GRCh38#50200054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94828603-C-A

50200054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 94828603-C-T

50200319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94828349-T-C

50200319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94828349-T-G

http://identifiers.org/hco/17/GRCh38#50201343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94827342-C-A

50201343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94827342-C-T

50201381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94827301-T-A

50201550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94827156-G-A

50201550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94827156-G-T

50201632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94827076-T-C

50201632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2197
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94827076-T-G