30284990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54793856-G-A

30284990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54793856-G-T

30285009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54793872-T-C

http://identifiers.org/hco/7/GRCh38#30285017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54793880-C-A

30285017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54793880-C-T

30285067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54793924-G-A

http://identifiers.org/hco/7/GRCh38#30285405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54794045-C-A

30285405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 54794045-C-G

30285405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 54794045-C-T

30285501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54794120-G-A

30285501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54794120-G-C

30285501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54794120-G-T

30285541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54794160-T-A

30285541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54794160-T-C

30285727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54794352-G-A

30285727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54794352-G-T

http://identifiers.org/hco/7/GRCh38#30285744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54794375-C-A

30285744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54794375-C-G

30285744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54794375-C-T

http://identifiers.org/hco/7/GRCh38#30285765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54794396-C-A

30285765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54794396-C-G

30285765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54794396-C-T

30286058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54794509-A-T

30286111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54794539-C-G

30286187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54794613-C-T

30286394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54794842-C-T

30286426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54794875-A-T

30287136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54795659-C-G

30287363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54795883-T-A

30287367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54795891-A-G

30287565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54796070-C-T

http://identifiers.org/hco/7/GRCh38#30288024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54796380-A-C

30288142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54796503-A-T

http://identifiers.org/hco/7/GRCh38#30288247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54796627-A-C

30288474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54796844-A-T

30288599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54796956-C-T

30288646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54797011-T-C

http://identifiers.org/hco/7/GRCh38#30289003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54797372-A-C

30289050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54797419-A-G

http://identifiers.org/hco/7/GRCh38#30289428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54797746-A-C

30289534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54797847-C-G

http://identifiers.org/hco/7/GRCh38#30289649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54797970-C-A

30289649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54797970-C-T

30289688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54798011-T-G

30289692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54798015-G-A

30289874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54798101-A-G

30289889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 54798116-C-T

30290052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54798231-T-C

http://identifiers.org/hco/7/GRCh38#30290128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54798318-A-C

30290457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54798622-G-C

30293622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54802925-C-T

30293729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54803022-G-A

30293911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54803158-C-G

30294390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54803598-T-C

30294630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54803870-A-G

30294738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54803967-T-C

30294786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54804019-G-A

http://identifiers.org/hco/7/GRCh38#30300554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54812452-A-C

30300651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54812541-C-G

30300651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54812541-C-T

30303957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54816992-A-G

30303975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54817005-C-G

30303975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54817005-C-T

30304228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54817214-G-A

30304312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54817288-G-T

30306117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54818955-T-C

30306173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54819013-T-G

30306280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54819065-T-A

30306282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54819067-G-T

30306520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54819181-T-G

30306804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54819434-G-A

30306899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54819526-T-A

30306951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54819578-A-G

30307007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54819644-A-G

30307337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54819993-T-G

30307369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54820034-A-G

30307369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54820034-A-T

30307607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54820331-G-T

30308017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54820713-G-T

30308349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54821235-A-G

http://identifiers.org/hco/7/GRCh38#30308373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54821253-A-C

30308373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54821253-A-G

30308373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54821253-A-T

30308473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54821317-T-C

http://identifiers.org/hco/7/GRCh38#30308648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54821506-C-A

30308790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54821657-C-T

30308930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54821807-A-G

30309191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54822045-T-C

30309367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54822312-C-T

30309500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54822423-A-G

30309707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54822605-T-C

30309743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54822639-T-A

http://identifiers.org/hco/7/GRCh38#30310150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54823146-A-C

30310399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54823361-T-G

30310418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54823379-G-C

30311573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54823903-C-T

30312602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54824731-T-C

30312628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54824757-A-G

30312983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54825024-A-G

30312992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54825027-G-A

30313158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54825183-A-G

30313168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54825193-G-A

30313168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54825193-G-C

30313210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54825238-G-A

30313269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54825294-G-A

30315744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54826691-G-A

30315744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54826691-G-C

30315744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54826691-G-T

30315921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54826908-A-G

30316778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54827393-C-T

30316913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54827521-T-G

30317294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54827851-A-T

30317305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54827862-G-A

30317305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54827862-G-T

30317401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54829104-T-C

30317407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54829110-T-A

30321231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54838336-A-T

30321326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54838425-T-C

30322294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54838726-C-T

30322333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54838768-C-T

http://identifiers.org/hco/7/GRCh38#30323499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54840737-C-A

30323499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54840737-C-G

30323499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54840737-C-T

30323539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54840782-G-A

30323550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54840793-G-T

http://identifiers.org/hco/7/GRCh38#30323573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54840816-C-A

30323573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54840816-C-T

30323576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54840819-G-A

30323576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54840819-G-T

http://identifiers.org/hco/7/GRCh38#30323594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54840837-C-A

http://identifiers.org/hco/7/GRCh38#30323730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54840973-C-A

30324950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54841866-A-G

30324953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54841869-T-C

30325759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54842740-T-C

30327908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54843600-A-G

http://identifiers.org/hco/7/GRCh38#30327947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54843633-C-A

30328550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54844152-G-A

30328550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54844152-G-T

30336793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54845948-C-T

30336816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54845970-G-C

30349472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54848023-G-A

30349534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54848076-A-T

30349742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54848309-A-T

30350167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54848677-T-C

30350233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54848741-G-A

30350312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54848905-A-G

http://identifiers.org/hco/7/GRCh38#30351095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54849726-C-A

30351376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54849961-A-G

30351490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54850209-G-T

30351563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54850326-A-G

30351563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54850326-A-T

30352205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54850987-A-G

30353257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54851734-T-C

30354823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54854152-C-T

30355022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54854700-T-G

30355030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54854707-T-C

30355523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54855155-G-A

30355613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54855238-A-G

30355750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54855356-T-C

30355935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54855551-T-C

30355957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54855573-A-T

30355978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54855594-A-G

30355978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54855594-A-T

30355979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54855595-T-C

30356246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54855810-C-G

http://identifiers.org/hco/7/GRCh38#30356267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54855830-C-A

30360825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54859895-T-C

30360826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54859896-G-A

30361011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54860069-C-T

30361334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54860341-G-A

30361353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54860357-C-T

30361484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54860473-A-G

http://identifiers.org/hco/7/GRCh38#30361940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54861323-A-C

30361940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861323-A-G

30361973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861361-G-A

30362193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861560-T-C

30362276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861642-T-C

30362281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861647-A-T

30362286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861652-A-T

30362326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861703-A-G

30362337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861709-G-A

http://identifiers.org/hco/7/GRCh38#30362342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54861714-A-C

30362342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861714-A-G

30362342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861714-A-T

30362343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861715-G-A

30362343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861715-G-T

30362344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861716-T-C

30362346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861718-T-C

30362354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54861727-T-C

30362389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54861762-A-G

30362425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 54861798-T-C

30362438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54861813-T-C

30362443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54861818-T-C

30362443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54861818-T-G

30362444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 54861819-T-C

30362454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 54861829-T-C

30362463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 54861846-T-C

http://identifiers.org/hco/7/GRCh38#30362548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54861934-C-A

30362548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54861934-C-T

30362553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54861939-G-A

30364770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54864653-T-C

30364771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54864654-T-C

30365071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54864846-A-G

30365139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54864886-C-T

30365152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54864899-T-C

30365220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54864920-A-T

30365233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54864933-G-A

30365267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54864965-A-G

http://identifiers.org/hco/7/GRCh38#30365292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#54864989-A-C

30365292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54864989-A-G

30365292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54864989-A-T

30365844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54865182-T-G

30365902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: intron variant
orthologous variants: 54865262-T-G

30365980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 54865336-A-T

30366271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3 prime UTR variant
orthologous variants: 54865641-C-T

30366390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3 prime UTR variant
orthologous variants: 54865762-G-A

30366390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3 prime UTR variant
orthologous variants: 54865762-G-T

30366861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 54866274-A-G

http://identifiers.org/hco/7/GRCh38#30366865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#54866278-C-A

30367689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22316
most severe consequence: 3 prime UTR variant
orthologous variants: 54867088-A-G