http://identifiers.org/hco/12/GRCh38#108288740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749140-C-A

108288740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749140-C-G

108288740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749140-C-T

108288757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749157-T-C

http://identifiers.org/hco/12/GRCh38#108288771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749178-C-A

108288786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749193-T-A

108288786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749193-T-C

http://identifiers.org/hco/12/GRCh38#108288789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749196-C-A

108288789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749196-C-T

http://identifiers.org/hco/12/GRCh38#108288793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749200-C-A

108288793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749200-C-T

108288845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749252-G-C

108288845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749252-G-T

http://identifiers.org/hco/12/GRCh38#108288895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749307-C-A

http://identifiers.org/hco/12/GRCh38#108288907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749319-C-A

108288908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749320-T-C

http://identifiers.org/hco/12/GRCh38#108289078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749412-C-A

108289097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749421-T-C

http://identifiers.org/hco/12/GRCh38#108289101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749425-C-A

108289101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749425-C-T

http://identifiers.org/hco/12/GRCh38#108289116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749440-C-A

108289116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749440-C-T

http://identifiers.org/hco/12/GRCh38#108289184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749506-C-A

108289184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749506-C-T

http://identifiers.org/hco/12/GRCh38#108289224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749542-C-A

http://identifiers.org/hco/12/GRCh38#108289301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749600-C-A

108289301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749600-C-T

108289320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749631-G-T

108289324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749635-G-A

108289324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749635-G-T

108289340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749651-C-T

108289392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749691-T-C

http://identifiers.org/hco/12/GRCh38#108289393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749692-A-C

http://identifiers.org/hco/12/GRCh38#108289406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749705-C-A

108289407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749706-T-A

http://identifiers.org/hco/12/GRCh38#108289412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749711-C-A

108289412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749711-C-T

http://identifiers.org/hco/12/GRCh38#108289413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749712-A-C

108289413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113749712-A-T

http://identifiers.org/hco/12/GRCh38#108289588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749880-C-A

http://identifiers.org/hco/12/GRCh38#108289642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113749933-C-A

http://identifiers.org/hco/12/GRCh38#108289690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113750001-A-C

108289861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750163-T-C

108289878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750179-C-T

108289888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750189-G-A

108289888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750189-G-T

http://identifiers.org/hco/12/GRCh38#108289912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113750210-A-C

108289917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750215-G-T

http://identifiers.org/hco/12/GRCh38#108290109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113750365-C-A

108290145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750397-A-G

http://identifiers.org/hco/12/GRCh38#108290256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113750507-C-A

108290256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750507-C-T

108290284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750535-G-T

108290324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750575-T-C

108290325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750576-G-A

http://identifiers.org/hco/12/GRCh38#108290335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113750586-C-A

108290569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750763-C-T

108290712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113750847-G-T

http://identifiers.org/hco/12/GRCh38#108290842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113750954-C-A

http://identifiers.org/hco/12/GRCh38#108290983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113751106-C-A

http://identifiers.org/hco/12/GRCh38#108290998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113751130-C-A

108290998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751130-C-T

108291019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751146-G-C

108291020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751156-G-A

108291020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751156-G-T

108291050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751189-G-A

108291050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751189-G-T

http://identifiers.org/hco/12/GRCh38#108291096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113751236-C-A

108291096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751236-C-T

108291137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751277-T-C

108291202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751366-T-C

http://identifiers.org/hco/12/GRCh38#108291209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113751373-C-A

108291209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751373-C-T

108291248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751412-T-C

http://identifiers.org/hco/12/GRCh38#108291249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113751413-C-A

http://identifiers.org/hco/12/GRCh38#108291253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113751417-C-A

108291260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751424-G-A

108291260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751424-G-C

108291260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751424-G-T

108291299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751463-G-A

108291306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751470-T-C

108291388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751493-G-A

108291405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751509-T-G

108291473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751544-G-C

http://identifiers.org/hco/12/GRCh38#108291521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113751581-C-A

108291562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751625-G-A

108291562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751625-G-T

108291579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751641-C-T

108291633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751700-T-C

http://identifiers.org/hco/12/GRCh38#108291634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113751701-C-A

108291742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751781-T-C

108291808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 3 prime UTR variant
orthologous variants: 113751851-G-C

108291907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113751950-G-A

108291907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: missense variant
orthologous variants: 113751950-G-C

108291955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113751998-A-G

108291955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: missense variant
orthologous variants: 113751998-A-T

108292177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752220-A-G

108292204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752247-G-A

108292240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752283-G-A

108292300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752343-A-G

http://identifiers.org/hco/12/GRCh38#108292327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113752370-C-A

http://identifiers.org/hco/12/GRCh38#108292414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113752457-C-A

108292414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752457-C-T

108292438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752481-G-A

108292506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: missense variant
orthologous variants: 113752549-C-T

108292543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752586-A-G

108292666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752709-G-A

108292741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752784-G-A

108292747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752790-T-A

108292747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752790-T-C

108292747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752790-T-G

108292771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752814-A-G

108292789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: missense variant
orthologous variants: 113752832-A-T

108292915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: 113752958-A-G

http://identifiers.org/hco/12/GRCh38#108292918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113752961-A-C

108293057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113753081-G-T

108295684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113757300-G-T

108295733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113757333-G-A

108298633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113760413-G-A

108298811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113760508-G-A

108298867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113760556-C-G

108298873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113760564-C-T

108298884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113760590-G-T

108298899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113760604-C-T

http://identifiers.org/hco/12/GRCh38#108298946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113760655-C-A

108299145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113760828-C-T

108301477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113762451-C-T

108301629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113762612-G-A

http://identifiers.org/hco/12/GRCh38#108301651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113762635-A-C

108301656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113762640-G-A

108301656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113762640-G-C

108301763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113762691-C-T

108302211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113763123-G-A

108302586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113763465-C-T

108303060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113764406-T-C

http://identifiers.org/hco/12/GRCh38#108303131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#113764476-C-A

108303131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron_variant, undefined
orthologous variants: 113764476-C-T

108303330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113764608-G-C

108303429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113764700-A-G

108303637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113764898-G-A

108303950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113765161-C-T

http://identifiers.org/hco/12/GRCh38#108303998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113765202-C-A

108303998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113765202-C-T

108304258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113765317-G-A

108304345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113765359-G-C

108304408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113765408-T-C

108304913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113765725-G-A

108305037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113765847-A-T

http://identifiers.org/hco/12/GRCh38#108305041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113765851-C-A

108305149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113765943-T-G

http://identifiers.org/hco/12/GRCh38#108305205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113765998-A-C

108305205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113765998-A-G

108305300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113766089-A-G

108305848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113766423-G-A

108305850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113766425-C-T

108306056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113766625-C-T

108306090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113766657-G-A

108308021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113768302-G-A

108308034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113768315-C-T

108308206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113768464-G-A

108308370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113768601-C-T

108308645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113768838-T-C

108308650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113768845-T-C

108308657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113768852-T-C

108308665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113768860-G-A

108308863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113769030-C-G

108308911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113769069-T-G

108308918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113769072-C-T

108309031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113769146-G-T

108309419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113769450-T-C

108310062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113769970-G-A

108310062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113769970-G-C

108310156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113770083-T-A

108310156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113770083-T-C

108310269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113770146-G-A

108310353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113770204-C-G

108310488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113770314-C-T

108312947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113771087-T-G

108312959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113771097-G-A

108313004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113771127-C-T

108313160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113771251-G-A

108313421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113771495-C-T

108313456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113771622-G-T

108313510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113771828-A-G

108313526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113771843-G-C

108313643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron_variant, undefined
orthologous variants: 113771950-C-T

108313691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron_variant, undefined
orthologous variants: 113771984-A-G

108313713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron_variant, undefined
orthologous variants: 113772004-T-C

108313715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron_variant, undefined
orthologous variants: 113772006-C-T

108314050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113772290-C-T

108314159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113772384-C-G

http://identifiers.org/hco/12/GRCh38#108317284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113774205-C-A

http://identifiers.org/hco/12/GRCh38#108317835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113774649-C-A

108317835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113774649-C-T

http://identifiers.org/hco/12/GRCh38#108317866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113774681-C-A

108317866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 113774681-C-G

108318080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113774852-T-C

108318168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113774987-T-C

http://identifiers.org/hco/12/GRCh38#108318747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113775563-C-A

108318749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113775565-A-G

108318935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113775745-G-A

108319041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113775837-C-T

108319286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113776114-C-T

http://identifiers.org/hco/12/GRCh38#108319620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113776417-A-C

108321687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113777273-T-A

108324411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113777504-T-C

http://identifiers.org/hco/12/GRCh38#108324604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113777789-C-A

108329126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113779998-T-A

http://identifiers.org/hco/12/GRCh38#108329270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113780127-C-A

108329270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113780127-C-T

108329648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113780496-G-A

108329740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113780590-T-G

108329871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113780747-G-T

http://identifiers.org/hco/12/GRCh38#108330015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113780883-A-C

http://identifiers.org/hco/12/GRCh38#108330076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113780942-C-A

108330077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 113780943-A-G

108330105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 113780971-G-A

108333488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113782853-G-T

108333888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113783086-G-A

108334661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113783849-A-G

108334661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113783849-A-T

108334681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113783879-G-A

108334865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113784063-T-C

108334942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113784124-G-A

108334942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113784124-G-T

108335043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113784201-T-C

108335205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113784324-C-T

108335413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113784508-T-A

108335413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113784508-T-C

108336094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113785504-A-G

108336124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113785529-T-C

108336137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113785536-G-C

108336295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113785737-C-T

108336298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113785740-G-A

108336388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113785816-T-C

108336500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113785876-T-C

http://identifiers.org/hco/12/GRCh38#108336922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113786293-C-A

108337203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113786419-C-G

108337507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron_variant, undefined
orthologous variants: 113786666-A-G

108337646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113786753-G-C

108337841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron_variant, undefined
orthologous variants: 113786918-G-A

108337967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113787028-G-A

108338512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113787707-G-A

108338539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: intron variant
orthologous variants: 113787736-G-A

108339063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 5 prime UTR variant
orthologous variants: 113788305-G-A

http://identifiers.org/hco/12/GRCh38#108339201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2121
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#113788411-C-A