http://identifiers.org/hco/3/GRCh38#172904099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26992745-C-A

172904543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26992424-C-T

172904946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26991733-C-T

172904984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26991686-C-T

172905067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26991614-G-A

172905208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26991480-T-G

172905280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26991408-G-A

http://identifiers.org/hco/3/GRCh38#172905359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-A

172905559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26991126-C-T

172905565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26991120-T-C

172905597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26991090-T-C

172906015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 26990684-C-T

172908077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26988144-G-T

172908454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26987770-G-A

172908454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26987770-G-C

172908454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26987770-G-T

172908905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26987334-T-C

172909382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26986844-T-C

172909382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26986844-T-G

172909606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26986676-G-A

172909871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26986447-C-T

172909938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26986384-A-G

172910476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26986213-G-A

172910476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26986213-G-C

172910603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26986098-C-G

172910714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26985991-T-C

http://identifiers.org/hco/3/GRCh38#172910856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26985782-C-A

172910897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26985740-C-T

172910904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26985733-C-G

172910918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26985687-G-A

172911023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26985446-T-A

http://identifiers.org/hco/3/GRCh38#172911228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26985070-A-C

http://identifiers.org/hco/3/GRCh38#172911328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26984967-C-A

172911342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26984953-C-T

172911394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26984903-A-G

172911418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26984879-A-G

172911536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26984646-T-C

172911746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26984432-T-G

172912917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26982591-G-A

172912922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26982586-C-T

172913045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26982463-A-T

172913046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26982462-T-A

http://identifiers.org/hco/3/GRCh38#172913205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26982311-C-A

172913267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26982270-T-G

172913282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26982255-T-C

http://identifiers.org/hco/3/GRCh38#172913471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26981737-A-C

http://identifiers.org/hco/3/GRCh38#172913523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26981679-C-A

172913523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26981679-C-T

172913693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 26981504-T-C

172913757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26981440-G-A

172913757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26981440-G-T

172913865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26981332-T-A

172913865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26981332-T-C

172913885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26981312-C-T

http://identifiers.org/hco/3/GRCh38#172913886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26981311-C-A

172913886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26981311-C-T

172914131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26981064-T-C

172915214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26979443-T-C

172915221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26979436-A-G

172915405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26979247-G-A

172915405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26979247-G-C

172915522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26979130-G-C

172915709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26978959-T-C

http://identifiers.org/hco/3/GRCh38#172916278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26978584-C-A

172916278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26978584-C-T

172916420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 26978439-T-C

172916420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 26978439-T-G

172916522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26978336-G-A

172916540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26978323-A-G

172916557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26978302-C-G

172916700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26976672-A-G

172916874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26976516-A-G

172917302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26976150-A-G

172917563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975941-C-T

172917614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975889-G-C

172917652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975852-A-T

172917687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975819-A-G

172917827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975695-C-T

http://identifiers.org/hco/3/GRCh38#172917856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26975668-A-C

172917881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975643-A-G

172917888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975636-T-C

172918147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975404-C-G

172918162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975389-C-G

172918183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975368-G-A

172918183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975368-G-C

172918188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975362-A-G

172918188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26975362-A-T

172918764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26974785-A-T

172919008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26974539-A-G

172919182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26974370-C-G

172920322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26974086-T-C

172920867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26973565-A-G

http://identifiers.org/hco/3/GRCh38#172921076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26973394-C-A

172921076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26973394-C-T

172921286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26973240-C-T

172921342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26973185-C-G

172921342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26973185-C-T

172921433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26973108-C-T

172921592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26972967-T-A

172921592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26972967-T-G

172921677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26972892-C-G

172922063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26972667-A-G

http://identifiers.org/hco/3/GRCh38#172922174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26972580-A-C

172922500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26971768-G-A

172923165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26970034-T-C

172923213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26969986-A-G

172923739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26969482-A-T

172923836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26969384-A-T

172923849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26969371-C-T

172923886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26969338-T-C

http://identifiers.org/hco/3/GRCh38#172923984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26969222-A-C

http://identifiers.org/hco/3/GRCh38#172924125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26969049-C-A

172924734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26968463-G-A

172924861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26968337-T-C

172924960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26968264-C-T

172924980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26968244-A-T

172924986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26968238-G-T

172925306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26967546-G-C

172925354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 26967472-A-G

172925580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26967250-T-C

172925611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26967206-G-A

172925611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26967206-G-T

172926370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26965526-G-C

http://identifiers.org/hco/3/GRCh38#172927032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26965035-A-C

172927032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26965035-A-G

http://identifiers.org/hco/3/GRCh38#172927114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26964970-A-C

172927137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26964947-C-T

172927198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26964830-C-T

172927379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26964634-G-A

172928825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26963606-G-A

172928825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26963606-G-T

172928975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26963465-T-C

172929159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26963295-A-G

172929242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26963235-A-T

172929448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26963032-A-G

172929519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26962979-C-T

172929521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26962977-C-T

172931650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26954434-G-A

172931650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26954434-G-T

172932432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26953101-A-G

172932546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26952988-A-G

http://identifiers.org/hco/3/GRCh38#172932869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26952544-C-A

172932877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26952536-T-G

172933015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26952401-T-A

172933109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26952311-T-C

172933109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26952311-T-G

172949261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26946272-G-T

172949307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26946235-A-G

172949326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26946217-A-T

172950170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26944929-G-T

172950174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26944925-T-C

172950183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26944916-G-T

172950343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26944781-T-G

http://identifiers.org/hco/3/GRCh38#172950393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26944731-A-C

172950974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26944143-A-G

172950987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26944130-T-G

172951265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26943855-T-G

172952080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26942873-G-C

172952168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26942361-A-T

172954629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26935527-G-A

172954752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26935400-A-G

http://identifiers.org/hco/3/GRCh38#172954847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26935294-C-A

172955224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26934914-T-A

172955358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26934787-T-A

172955745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26934085-C-T

172956044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26933793-A-T

172956173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26933668-A-G

172956179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26933662-A-T

172956285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26933238-G-C

172956285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26933238-G-T

172956378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26933151-A-G

172956451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26933070-C-G

172956520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26933008-A-G

172956655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26932878-A-G

172956655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26932878-A-T

172956684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 26932850-C-T

172956694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 26932840-G-T

172956700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 26932834-G-A

172956934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26932600-T-C

172957265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26932288-A-G

172957436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26932135-C-T

172957790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26931772-C-G

http://identifiers.org/hco/3/GRCh38#172958083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26930170-C-A

172958083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26930170-C-T

172958194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26930071-T-C

172958444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26929922-G-A

172958468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26929899-G-A

172958679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26929686-C-T

172959156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26929145-G-A

172959358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26928946-C-T

172959445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26928857-C-G

172959445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26928857-C-T

172959447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26928855-C-G

172959520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26928788-G-A

172960339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26911945-T-C

172960566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26911729-C-G

172960566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26911729-C-T

172960947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26911457-C-T

172961797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26911122-C-T

172961805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26911114-C-T

172962050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910902-C-G

172962050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910902-C-T

172962059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910891-C-T

172962206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910766-T-C

172962230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910754-G-A

172962230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910754-G-T

http://identifiers.org/hco/3/GRCh38#172962232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#26910752-C-A

172962232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910752-C-T

172962531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910520-C-T

172962751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910307-G-A

172963018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910069-A-T

172963076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910008-G-C

172963077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26910007-T-C

172963111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26909973-T-C

172963600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26908701-G-C

172963612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26908689-T-C

172964068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26908253-T-C

172964121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26908213-A-T

172964196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26908140-C-T

172964234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26908103-T-C

172965161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 26907574-T-C

http://identifiers.org/hco/3/GRCh38#172966133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#26906869-A-C

172966735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26906317-C-G

172966735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26906317-C-T

172967152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26905882-T-G

172967156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26905878-G-A

172968519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26905232-G-A

172969022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26904713-T-A

172969022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26904713-T-C

172969429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26904387-T-C

172969578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902927-A-G

172969591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902915-C-T

172969715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902802-T-C

172969717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902800-G-A

172969731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902786-T-C

172969787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902748-G-A

172969830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902708-G-A

172969944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902597-G-A

172969992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902555-C-G

172970123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902435-T-C

172970243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26902348-T-A

172970608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26901989-A-G

172970627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26901968-G-C

172970664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26901934-T-A

http://identifiers.org/hco/3/GRCh38#172970764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26901831-C-A

172970903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26901684-G-A

http://identifiers.org/hco/3/GRCh38#172970947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26901639-C-A

172971072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26901520-A-G

172971072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26901520-A-T

172971197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26901409-A-G

172971404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26900921-T-C

172971596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26900002-C-G

172971596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26900002-C-T

172971605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26899993-C-T

172971943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26899696-C-G

172972152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26899495-T-G

172972484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26899163-T-A

172972910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26898773-G-T

172972986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26898698-C-T

172973190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26898520-T-C

172973191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26898519-G-A

172973286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26898429-T-C

172973325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26898390-C-T

172973441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26898250-G-A

172973733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26897971-T-C

172973788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26897674-G-A

172975086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26896250-T-C

172975402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26896061-G-A

172975413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26896050-T-C

172975491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26895991-C-T

http://identifiers.org/hco/3/GRCh38#172975500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26895982-C-A

172975563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26895931-G-A

172976553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26895264-A-G

172976584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26895231-T-C

172976602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26895213-A-G

172976604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26895211-A-G

172976863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26894956-A-G

http://identifiers.org/hco/3/GRCh38#172976883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26894936-C-A

172976883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26894936-C-T

172976951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26894903-G-T

172976952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26894902-G-T

172976957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26894897-T-A

172976972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 26894882-C-T

http://identifiers.org/hco/3/GRCh38#172977199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26894664-A-C

172977199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26894664-A-G

http://identifiers.org/hco/3/GRCh38#172977200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26894663-C-A

172977200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26894663-C-T

172977238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26894624-G-A

172977361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26894505-A-G

172978082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26893698-A-G

172978148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26893389-T-C

172978152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26893385-T-C

http://identifiers.org/hco/3/GRCh38#172978161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26893375-C-A

172978161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26893375-C-T

http://identifiers.org/hco/3/GRCh38#172978163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26893373-A-C

172978176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26893360-A-T

172978182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26893354-G-C

172978376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26893060-A-G

172978494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26892955-T-C

172978581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26892861-G-A

172980196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26892566-T-C

172980200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26892562-G-C

172980223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26892531-T-C

172981106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26891796-C-T

172981505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26890162-C-T

172981615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26890054-G-A

172981865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26889772-C-G

172981877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26889760-C-T

172982105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26889538-A-G

172982159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26889500-A-G

172982491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26889182-C-T

172982577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26889073-T-C

172982695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26888950-A-G

172982752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26888914-A-G

172983120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26888544-C-T

172983220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26888446-T-A

172983318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26888345-A-G

172983321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26888342-G-T

172983758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887841-C-G

172983943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887645-G-A

172983943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887645-G-T

172983960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887628-T-A

172983960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887628-T-C

172983972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887616-G-C

172984079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887518-A-G

172984083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887514-G-A

172984258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887342-G-A

172984260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887340-C-T

172984287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26887313-G-A

172984718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26885927-G-A

172984727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26885918-G-A

http://identifiers.org/hco/3/GRCh38#172984976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26885668-A-C

172985163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26885409-T-C

172985178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26885394-A-G

172985752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26883646-G-A

172986033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26883370-T-C

172986310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26883177-A-G

172986476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882999-G-A

172986476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882999-G-T

172986654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882854-A-G

172986678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882840-G-A

172986697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882821-C-T

172986798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882720-T-C

172987020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882558-G-A

172987191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882436-A-G

172987197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882430-G-A

172987230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882397-G-A

http://identifiers.org/hco/3/GRCh38#172987313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26882315-C-A

172987313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26882315-C-T

172988555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26881200-C-T

172988903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26880937-G-A

http://identifiers.org/hco/3/GRCh38#172988925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26880919-C-A

172988966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26880879-G-A

http://identifiers.org/hco/3/GRCh38#172989465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26880443-C-A

172989505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26880403-G-A

172989629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26880286-A-G

172989629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26880286-A-T

http://identifiers.org/hco/3/GRCh38#172989672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26880245-A-C

172990100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26878646-A-G

172990184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26878566-G-A

172990251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26878502-A-G

172990648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26878244-G-A

172990689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26878203-G-A

http://identifiers.org/hco/3/GRCh38#172990811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26878080-C-A

172991051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26877765-C-T

172991820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26876960-T-C

172992044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26876739-T-C

172992159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26876631-G-T

172992564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26874239-A-G

172992768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26874054-C-T

172992839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873958-G-A

172992975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873841-A-G

172993093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873709-C-T

172993184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873628-G-A

172993205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873602-A-T

172993208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873599-A-T

172993401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873417-A-G

172993521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873300-A-G

172993573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873268-C-G

172993629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873213-T-C

172993629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26873213-T-G

172993871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26872977-G-A

172993871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26872977-G-C

172994176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26872690-C-T

172994177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26872689-C-G

172994632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26872071-C-T

172994946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26871772-T-A

172995302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26870290-G-A

172995380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26870234-A-G

172996421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26869011-G-A

172996837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26868603-T-C

173003005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26856687-T-A

173003057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26856637-C-G

173003080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26856620-T-G

173003468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26856259-C-G

173003485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26856242-C-T

173003490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26856237-G-A

173003490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26856237-G-T

173003611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26856122-G-A

173003611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26856122-G-T

173003690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26856021-T-G

173003721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26855984-T-C

173003783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26855844-C-T

173003899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26855587-A-T

173004254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26855206-A-G

http://identifiers.org/hco/3/GRCh38#173004424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26855035-A-C

173004424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26855035-A-G

173004481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26855000-G-C

173004495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26854986-C-T

173004518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26854963-C-G

173004518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26854963-C-T

173004519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26854962-C-T

173005981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26852031-G-C

173006292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26851708-A-T

173006418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26851599-G-A

173006952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26850925-A-T

173007025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26850855-C-T

173007221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26850614-C-T

173008331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26849278-A-G

173016280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26834707-A-G

173016314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26834674-G-A

173016417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26834580-T-C

173016498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26834499-G-C

173016553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26834443-C-T

173016601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26834395-G-A

173016658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26834345-A-G

http://identifiers.org/hco/3/GRCh38#173016997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26834230-C-A

173017300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26834005-T-A

173017327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26833978-C-G

173017512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26833807-A-G

173017528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26833792-T-C

173018560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26832632-C-T

173018848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26832362-A-T

173018922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26832301-A-G

173019284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26831943-T-C

173019474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26831753-A-G

173019522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: missense variant
orthologous variants: 26831705-A-G

173019522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: missense variant
orthologous variants: 26831705-A-T

http://identifiers.org/hco/3/GRCh38#173019688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26831543-A-C

173019688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26831543-A-T

173019821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26831434-A-G

173019821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26831434-A-T

173019831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26831424-G-C

http://identifiers.org/hco/3/GRCh38#173020238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26831135-A-C

173020238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26831135-A-G

173020331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26831086-A-G

173020877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26830555-T-A

http://identifiers.org/hco/3/GRCh38#173021082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26830373-C-A

173021308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26830243-C-G

173021308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26830243-C-T

173021339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26830212-G-A

173021365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26830186-G-A

173021418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26830133-T-G

173021489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26830061-A-G

http://identifiers.org/hco/3/GRCh38#173021490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26830060-C-A

173021801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26829811-T-A

173021847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26829782-A-G

173021852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26829777-G-T

173021857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26829772-G-A

173022098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26829581-A-G

173022105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26829574-G-A

173022679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26829038-T-A

173022679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26829038-T-G

http://identifiers.org/hco/3/GRCh38#173022714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26829011-C-A

173023114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26828639-T-A

173023858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26827289-C-T

http://identifiers.org/hco/3/GRCh38#173024100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26827108-A-C

173024100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26827108-A-T

173024385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26826849-T-A

173024551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26826772-A-G

173024615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26826732-A-G

173024738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26826648-G-A

173024738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26826648-G-T

173026884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26824225-C-T

173027299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26823812-T-G

173027344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26823768-A-T

173027439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26823678-C-T

173027714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26823413-C-T

173027751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26823386-C-T

173027814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26823274-G-A

173028580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26822771-A-G

173031116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26812162-T-G

173031370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26811913-G-C

173031370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26811913-G-T

173031429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26811853-A-G

173032421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26810853-C-T

173032676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26810623-A-T

173032679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26810620-C-G

173032679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26810620-C-T

173032966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26810367-G-A

173033221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26809611-A-G

http://identifiers.org/hco/3/GRCh38#173033656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26809177-A-C

173033674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26809162-G-A

173033674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26809162-G-T

173034179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26808971-T-G

173034186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26808964-T-G

173034354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26808793-T-C

173034374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26808773-G-T

173034591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26808567-C-T

173034778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26808335-T-G

173034871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26808244-T-C

173034886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26808239-A-G

173034944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26808200-C-T

173034953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26808191-A-G

http://identifiers.org/hco/3/GRCh38#173035637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26806285-A-C

173035637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26806285-A-G

173035692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26806224-G-T

173035698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26806218-G-C

173035935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26806039-T-C

173036832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26805133-G-T

173036996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26804983-A-G

173037654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26804118-A-T

173037872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26803903-C-T

173039667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26802297-G-A

173039771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26802219-T-C

173039791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26802201-C-T

173039893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26802090-G-T

173040095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26801762-C-G

173040098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26801759-C-G

http://identifiers.org/hco/3/GRCh38#173040099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26801758-C-A

173040721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26798660-G-A

http://identifiers.org/hco/3/GRCh38#173040776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26798593-A-C

173041029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26798324-A-G

173041043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26798310-T-A

173041048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26798305-A-G

173041141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26798212-G-A

173041217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26798146-T-G

173041235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26798128-C-G

http://identifiers.org/hco/3/GRCh38#173041256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26798106-C-A

http://identifiers.org/hco/3/GRCh38#173041490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26797891-A-C

173041490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26797891-A-G

173041595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26797772-T-C

http://identifiers.org/hco/3/GRCh38#173044726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26796659-A-C

http://identifiers.org/hco/3/GRCh38#173044748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26796638-A-C

173045061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26796369-A-G

173045070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26796360-G-C

173045324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26796011-G-T

173045593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26795750-C-T

173046093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26795325-T-C

173046419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26795011-T-A

173046505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26794890-T-G

173046781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26794621-T-A

173046847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26794555-C-T

173046861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26794541-T-G

173046942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26794463-C-G

http://identifiers.org/hco/3/GRCh38#173047288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26794141-C-A

173047288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26794141-C-T

173047349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26794080-A-G

173047723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26793825-G-C

173047723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26793825-G-T

173047754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26793795-T-A

http://identifiers.org/hco/3/GRCh38#173048204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26787752-A-C

173048434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26787532-T-A

173048582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26787427-C-T

173048624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26787384-G-A

173048731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26787276-C-T

173048779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26787241-G-C

http://identifiers.org/hco/3/GRCh38#173048939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26787092-A-C

173048940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26787091-T-C

173048940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26787091-T-G

173048979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: missense variant
orthologous variants: 26787052-T-C

http://identifiers.org/hco/3/GRCh38#173049021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26787010-A-C

173049021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: missense variant
orthologous variants: 26787010-A-G

173049060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: missense variant
orthologous variants: 26786971-A-G

173049069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: missense variant
orthologous variants: 26786962-C-G

173049075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: missense variant
orthologous variants: 26786956-A-G

173049106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26786928-A-G

173049382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26786726-A-G

173049689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26786423-G-A

173049872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26786244-C-T

173049896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26786221-A-G

173049971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26786141-C-G

173052225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26781837-G-C

173052405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26781629-G-T

173052509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26781525-T-C

173052546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26781492-T-C

173053033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26781073-G-A

173053488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26780677-A-G

http://identifiers.org/hco/3/GRCh38#173057820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26777319-A-C

173057864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26777280-T-A

173057882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26777266-A-G

173058020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26777125-C-T

173058161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26776990-A-G

173058227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26776918-A-G

173058280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26776872-A-G

173058307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26776840-A-G

173058564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26776509-A-G

173058653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26776422-A-G

173058675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26776400-T-A

173059020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26775761-T-A

173059151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26775636-T-C

173059182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26775632-T-C

173059337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26775525-G-A

173059337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26775525-G-T

173059596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26775376-T-G

173059652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26775291-T-G

173059668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26775275-T-A

173059929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26774958-A-G

173060129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26774762-C-T

173060513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26774146-G-T

173060695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26773965-C-T

173060717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26773942-G-T

173061045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26773625-T-C

173061266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26773388-A-G

173061523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26773023-C-T

173061637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772907-A-G

173061667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772878-G-A

173061679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772866-A-G

173061732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772815-A-G

173061732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772815-A-T

173061778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772770-G-A

173061781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772767-C-T

173061913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772633-A-G

173061963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772583-C-G

173062013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772533-C-T

http://identifiers.org/hco/3/GRCh38#173062084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26772470-A-C

http://identifiers.org/hco/3/GRCh38#173062212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26772342-A-C

173062315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772244-T-A

173062437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26772118-C-G

173062572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26771978-G-C

173062595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26771954-A-G

http://identifiers.org/hco/3/GRCh38#173062662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26771898-A-C

http://identifiers.org/hco/3/GRCh38#173062696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26771870-A-C

173062729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26771859-A-G

173062764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26771839-C-T

173063485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26771427-G-A

173063514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26771398-C-T

173064516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770971-C-G

173064516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770971-C-T

173064611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770772-G-T

173064780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770623-A-G

173064845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770564-A-G

173064999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770436-A-G

173065170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770275-G-A

173065273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770181-A-G

173065273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770181-A-T

http://identifiers.org/hco/3/GRCh38#173065310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26770154-A-C

173065310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770154-A-G

173076101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26770027-G-T

173076345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26769789-C-T

173076484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26769662-A-G

173076521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26769626-A-G

173076775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26769365-T-C

173076787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26769349-C-T

173076942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26769233-A-G

173077238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26768982-A-T

173077460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26768765-A-G

173077641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26768586-A-G

173077685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26768541-T-C

173077721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26768513-C-T

173077741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26768493-A-G

173078157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26768104-T-C

173078282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26767969-T-G

173078338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26767915-T-G

173079500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26766683-C-G

173079870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26765760-A-T

173080390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26764844-G-A

173080415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26764820-C-T

173080642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26764664-A-G

173080675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26764631-T-C

173080817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26764510-G-C

173080839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26764490-G-A

173080839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26764490-G-C

173080915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26764433-A-G

http://identifiers.org/hco/3/GRCh38#173080973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26764380-C-A

173080989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26764365-T-G

173081270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26763486-C-T

173081453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26763034-A-G

173081595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26762895-T-A

173081640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26762853-A-G

173089019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26760483-T-A

http://identifiers.org/hco/3/GRCh38#173089312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26760195-C-A

http://identifiers.org/hco/3/GRCh38#173089345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26760151-C-A

173089567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26759940-G-C

173089588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26759920-G-A

173089778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26759762-A-G

173090011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26759560-A-G

173090801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26752879-A-G

http://identifiers.org/hco/3/GRCh38#173090876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26752793-A-C

173090876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26752793-A-G

173091938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26749985-A-T

173091958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26749970-G-C

173092048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26749849-C-T

173092217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26749681-C-G

173092244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26749656-G-T

173092264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26749637-C-T

173092550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26749371-G-A

173092633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26749286-C-T

173092956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26748959-A-G

173093091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26748848-G-A

173093091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26748848-G-C

173093091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26748848-G-T

173093514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26748219-G-A

173093580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26748173-A-G

173093674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26748080-G-A

173093806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26747943-A-G

173093843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26747710-G-A

173093849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26747655-A-G

http://identifiers.org/hco/3/GRCh38#173093953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26747552-C-A

173093955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26747550-A-G

173094080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26747455-T-C

173094121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26747415-G-A

173094148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26747387-T-C

173094465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26747083-G-A

173094899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26746757-C-T

173094906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26746753-G-A

173094999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26746670-A-G

173095006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26746656-T-A

173095252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26746458-T-C

173095252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26746458-T-G

http://identifiers.org/hco/3/GRCh38#173095284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26746415-C-A

173095679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26741495-T-C

173095745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26741450-G-A

173095746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26741449-C-T

173095961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26741265-T-G

173096010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26741220-T-C

173096010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26741220-T-G

173096133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26741098-A-T

173096202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26741022-T-G

173096299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26740920-C-G

173096299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26740920-C-T

173096404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26740822-G-A

173096887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26740437-G-T

173096944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26740389-A-G

173099828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26740012-G-A

173099861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26739978-T-C

173099930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26739892-C-G

173100622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26739268-C-T

http://identifiers.org/hco/3/GRCh38#173100645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26739246-C-A

173100646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26739245-A-T

173100766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26739121-G-A

173100950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26738934-A-T

173100966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26738918-T-A

173101135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26738764-G-A

173101168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26738719-T-G

173101259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26738630-T-C

173105625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26738274-A-T

173105741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26738144-T-A

173105802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26738072-T-A

173106083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26737320-C-G

173106839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26736736-G-T

http://identifiers.org/hco/3/GRCh38#173106947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26736631-A-C

173107229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26734473-T-C

173107254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26734449-A-G

173107474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26734235-C-T

173107480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26734229-G-C

173107480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26734229-G-T

173107503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26734208-A-T

173107610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26734105-T-G

173107784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26733936-G-A

173108131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26733576-A-G

173108273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26733430-A-T

173108368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26733352-T-A

http://identifiers.org/hco/3/GRCh38#173108919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26732865-A-C

173109080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26732702-A-G

http://identifiers.org/hco/3/GRCh38#173109117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26732669-C-A

173109313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26732528-G-A

173109592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26732280-G-A

http://identifiers.org/hco/3/GRCh38#173109608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26732270-C-A

http://identifiers.org/hco/3/GRCh38#173110781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#26729716-C-A

173110796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26729702-G-A

173110868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26729622-T-C

173110868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26729622-T-G

173110873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26729617-T-C

173110946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26729537-T-G

173111024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26729486-C-T

173111057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26729468-A-G

173111071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26729462-G-A

173111519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26728141-A-G

173111519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26728141-A-T

173111613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26728071-T-A

173111613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26728071-T-C

173111624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26728060-G-A

173112145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26727091-C-T

173112146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26727090-A-T

173112348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26726519-C-G

173112392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26726475-G-A

173112475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26726381-C-T

173112746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26726121-C-G

173112873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26725999-T-C

173113738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26724878-G-T

173113774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26724842-G-A

173114223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26724701-T-C

173114240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron variant
orthologous variants: 26724684-G-A

173115103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26723882-G-T

173115320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26723649-G-A

173115386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26723573-C-T

173115393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26723561-T-C

173115410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26723544-C-T

173115578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26723371-C-G

173115586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26723363-C-T

173116426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26722751-G-A

173116445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26722732-A-G

173116451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26722726-C-T

173116724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26722454-C-T

173116920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26722282-T-C

173117041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26722169-G-A

173117041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26722169-G-T

173117062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26722148-T-C

173117095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26722118-A-G

173117343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 26721870-A-G

173117343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 26721870-A-T

173117400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 26721813-G-A

173117628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 26721582-G-A

173117628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 26721582-G-T

http://identifiers.org/hco/3/GRCh38#173117668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#26721542-C-A

173117668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 26721542-C-G

173117707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 26721503-A-G

173117756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 26721454-G-A

173117756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 26721454-G-C

173117756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 26721454-G-T

173117822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26721385-T-A

173117853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26721354-T-C

173117889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26721320-A-G

173118338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26720885-T-G

173118466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26720771-C-T

173118694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26720575-G-A

173118856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26720444-G-C

173118972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26720329-C-T

173120326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26719399-C-T

173120520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26719225-A-G

173120564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26719181-T-A

173120564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26719181-T-C

http://identifiers.org/hco/3/GRCh38#173120857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#26718897-C-A

173120957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26718796-T-C

173121178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26718567-G-A

173121178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26718567-G-T

173121359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26718420-G-A

173121376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26718403-T-G

173121838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26716639-G-A

173121838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26716639-G-T

http://identifiers.org/hco/3/GRCh38#173122249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#26716227-C-A

173122314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26716170-G-A

173122799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26715657-T-G

173122863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26715596-T-A

173123161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26715334-A-G

173123250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26715239-A-G

173123314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26715175-C-T

173123591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26714890-A-G

173124000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26714795-A-T

173124118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26714723-C-T

173124186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26714675-T-C

173124478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26714434-G-A

173124501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26714411-A-G

173124634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26713770-G-C

173124842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26713566-G-A

173124937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26713492-T-C

173125233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26713249-C-T

173125357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26713148-C-T

173125680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26712657-A-G

173125719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26712624-C-T

173125969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26712413-A-G

173125969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26712413-A-T

173125999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26712383-A-G

http://identifiers.org/hco/3/GRCh38#173126030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#26712353-C-A

173126030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26712353-C-G

173126030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26712353-C-T

173126175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26712186-C-T

173126355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26712001-G-A

173126415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26711943-T-C

173126461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26711897-A-G

173126488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26711850-G-T

173126490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26711848-T-C

http://identifiers.org/hco/3/GRCh38#173126695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#26711648-A-C

173126695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26711648-A-T

173126776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26711575-T-A

173127073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26710413-T-C

173127473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26709996-T-C

173130599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26708438-G-A

173131072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26708037-G-A

http://identifiers.org/hco/3/GRCh38#173131243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#26707900-C-A

173131243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26707900-C-T

173131784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26707229-T-C

173133105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26701247-A-G

http://identifiers.org/hco/3/GRCh38#173133129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#26701223-A-C

173133260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26701094-A-G

173136966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26697137-C-T

173137031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26696786-C-T

173137054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26696765-C-T

173137169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26696693-C-T

173137706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26696103-G-A

173137706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26696103-G-T

http://identifiers.org/hco/3/GRCh38#173137767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#26696051-C-A

173138016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26695933-A-G

173138028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26695921-T-G

173138729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26695213-G-T

173138882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26695056-G-A

173139129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26694818-G-A

173139162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26694785-A-G

173139582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26694362-C-T

173140247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26693114-A-G

173140510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29935
most severe consequence: intron_variant, undefined
orthologous variants: 26692879-A-G