36714959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 3 prime UTR variant
orthologous variants: 111318146-A-G

http://identifiers.org/hco/3/GRCh38#36714973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111318132-C-A

36715000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 3 prime UTR variant
orthologous variants: 111318106-A-G

36715000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 3 prime UTR variant
orthologous variants: 111318106-A-T

36715031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 3 prime UTR variant
orthologous variants: 111318076-A-G

36715372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111317740-G-A

36715372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111317740-G-C

36715386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111317726-G-A

36715539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111317570-G-A

36715539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111317570-G-C

36715548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111317561-G-A

36715590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111317515-G-A

36715590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111317515-G-T

http://identifiers.org/hco/3/GRCh38#36715630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111317475-C-A

36715630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111317475-C-G

http://identifiers.org/hco/3/GRCh38#36715634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111317471-A-C

36715658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111317441-G-A

36715658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111317441-G-T

36715673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111317431-A-G

36716314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111316010-G-C

36716335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111315984-G-C

http://identifiers.org/hco/3/GRCh38#36716339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111315980-C-A

http://identifiers.org/hco/3/GRCh38#36716344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111315975-C-A

36716397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111315927-G-A

http://identifiers.org/hco/3/GRCh38#36716399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111315925-C-A

http://identifiers.org/hco/3/GRCh38#36716430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111315894-C-A

36716432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111315892-G-A

36718108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111314052-G-C

36718162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111313998-A-T

36718234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313949-G-A

36718234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313949-G-T

36719200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313344-T-G

36719260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313292-T-C

36719360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313198-G-A

36719439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313114-A-G

36719439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313114-A-T

36719494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111313053-C-G

36719686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312864-C-T

36719710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312841-C-T

36719842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312716-T-A

36719974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312574-A-G

36719983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312565-C-G

http://identifiers.org/hco/3/GRCh38#36720864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111312458-C-A

36721003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312355-T-C

36721234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312155-C-G

36721260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111312136-T-C

36721553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111311790-A-G

36721553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111311790-A-T

36721562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 111311781-G-A

36726690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310764-C-T

36726843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111310322-A-T

http://identifiers.org/hco/3/GRCh38#36727995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111309303-A-C

36728150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309231-T-C

36728150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309231-T-G

36728283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111309079-T-C

http://identifiers.org/hco/3/GRCh38#36729214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111308942-A-C

36729269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308914-C-G

http://identifiers.org/hco/3/GRCh38#36729278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111308905-C-A

http://identifiers.org/hco/3/GRCh38#36729299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111308870-A-C

36729378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308806-C-T

36729421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308767-G-T

36729454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308735-T-C

36729590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308390-G-A

36729590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308390-G-T

36729630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308350-G-A

36729630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308350-G-C

36729652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111308188-A-G

36729687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308156-C-T

36729703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111308141-G-A

http://identifiers.org/hco/3/GRCh38#36729751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111308093-C-A

http://identifiers.org/hco/3/GRCh38#36729824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111308023-C-A

36732668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111306511-T-C

36732671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111306503-T-G

36733007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111306212-T-C

36733093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111306121-T-C

36733129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111306095-A-G

36733235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111306013-T-C

36733273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305974-A-G

36733281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305966-G-A

36733521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305766-A-G

36733701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305599-T-C

36733749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305556-C-T

36733815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305488-C-T

36733892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305408-G-A

36733938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305359-T-C

36733939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305358-G-A

36733953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305344-G-C

http://identifiers.org/hco/3/GRCh38#36734204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111305118-C-A

36734269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111305053-C-T

36734343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111304984-A-G

36734343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111304984-A-T

36734399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111304930-G-C

36734465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111304869-T-C

36734536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111304828-T-C

36734703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111304136-C-T

36734717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111304122-C-G

36734833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303982-A-G

36734931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303881-T-C

http://identifiers.org/hco/3/GRCh38#36735017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111303810-C-A

36735049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303766-C-T

36735072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303738-T-C

36735121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303704-G-A

36735129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303696-T-G

36735164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303660-C-T

36735519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303101-A-G

36735520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303100-C-T

36735626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303021-C-T

http://identifiers.org/hco/3/GRCh38#36735629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111303018-C-A

36735629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111303018-C-G

36735732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111302914-C-T

36735857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111302799-A-G

36735891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111302765-G-A

36735969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111302689-A-T

http://identifiers.org/hco/3/GRCh38#36736758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111299245-C-A

36736758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111299245-C-G

36737060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111298952-T-C

http://identifiers.org/hco/3/GRCh38#36737099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111298913-A-C

36737113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111298900-G-A

36737113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111298900-G-T

36737151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111298449-A-G

36737153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111298447-T-C

http://identifiers.org/hco/3/GRCh38#36737176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111298413-C-A

36737176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111298413-C-G

36737221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111298368-G-A

36737302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111298287-T-C

36737302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111298287-T-G

36737512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111298077-G-A

36737512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111298077-G-T

http://identifiers.org/hco/3/GRCh38#36737626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111297963-A-C

36737626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297963-A-G

36737658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: synonymous variant
orthologous variants: 111297931-T-C

http://identifiers.org/hco/3/GRCh38#36737661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111297928-C-A

36737661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: synonymous variant
orthologous variants: 111297928-C-T

36737698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297891-A-G

36737746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297870-A-G

36737885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297731-C-T

36737919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: synonymous variant
orthologous variants: 111297697-C-T

36737953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297663-G-A

36737967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: synonymous variant
orthologous variants: 111297649-A-G

36737967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297649-A-T

36737976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: synonymous variant
orthologous variants: 111297640-G-T

36738017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297599-T-C

36738045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297571-G-T

36738083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297533-T-C

http://identifiers.org/hco/3/GRCh38#36738181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111297435-C-A

36738181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297435-C-T

36738184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297432-A-G

36738271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297345-T-A

36738271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297345-T-C

36738403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111297213-T-C

36738793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 111296835-A-G

36738951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 111296677-G-A

36738951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 111296677-G-T

36738997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 111296631-C-T

36739120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111296509-G-A

36739120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111296509-G-T

36739969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111296047-C-G

36740519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111295592-C-T

http://identifiers.org/hco/3/GRCh38#36740619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111295321-C-A

36740925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111294962-T-C

http://identifiers.org/hco/3/GRCh38#36741051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111294839-A-C

36741245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111294700-C-T

http://identifiers.org/hco/3/GRCh38#36741637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111294353-C-A

36741637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111294353-C-G

36741728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111294265-C-T

http://identifiers.org/hco/3/GRCh38#36742013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111294048-A-C

36742013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111294048-A-G

36742051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111294011-C-T

36742102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111293968-C-T

36742541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111293557-G-A

36742541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111293557-G-T

36745460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111292217-G-A

36745586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111292091-C-T

36745614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111292063-G-A

36745758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111291917-G-A

36745963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111291728-T-C

36746716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111291076-C-T

36748235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111290008-A-G

36748239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111290004-G-C

36748243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111290000-A-G

36748247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111289996-C-T

36748282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111289956-T-A

36748282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111289956-T-C

http://identifiers.org/hco/3/GRCh38#36748291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111289947-C-A

36748335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111289900-G-A

36748660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111289573-T-A

36748660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111289573-T-C

36748702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111289554-C-T

36748882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111289404-T-C

http://identifiers.org/hco/3/GRCh38#36749036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111289266-C-A

36749135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111289176-G-A

36749399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111288973-T-C

36749606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111288154-A-G

36749703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111288082-T-C

36750533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111287183-G-A

36750672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111287041-C-G

36750677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111287036-A-G

36750797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111286928-A-T

36751096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111286654-G-T

36751150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111286612-T-G

36751153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111286609-A-G

36751169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111286593-T-G

36751254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111286529-A-G

36751409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111286391-T-C

36751409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111286391-T-G

36751560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111286283-T-C

36752744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111284499-A-G

http://identifiers.org/hco/3/GRCh38#36752780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111284473-A-C

36753053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111284247-A-T

36753121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111284183-T-A

36753121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111284183-T-G

36753139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111284165-A-T

36754084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111282974-T-C

36754320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111282759-T-A

36754592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111282495-G-A

http://identifiers.org/hco/3/GRCh38#36754715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111282381-A-C

36754771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111282337-T-A

http://identifiers.org/hco/3/GRCh38#36754846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111282267-A-C

36754848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111282265-T-C

36754896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111282225-C-T

36754930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111282191-A-G

http://identifiers.org/hco/3/GRCh38#36755067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111282082-A-C

36755133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111282036-A-G

36755486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111279877-T-A

36755647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111279651-G-C

36755924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111279271-A-G

36755979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111279220-G-A

36756283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111279099-A-G

36756567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111278839-G-T

36756767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111278659-G-A

36756844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111278559-G-A

36756851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111278552-A-G

36757035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111278147-T-C

36757387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111277655-G-A

36757629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111277441-G-C

36757872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111277193-A-G

36757916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111277149-C-T

36758176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111276893-C-T

36758281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111276808-T-C

http://identifiers.org/hco/3/GRCh38#36758837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111275473-C-A

36758837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111275473-C-T

36759086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111275243-C-T

36759279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111275019-C-T

36759308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111274761-G-T

http://identifiers.org/hco/3/GRCh38#36759580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111274529-A-C

36759585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111274523-C-T

36759686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111274427-T-C

36759715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111274401-T-C

36759783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111274335-C-T

36760242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111272792-G-C

36760872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111272510-C-T

http://identifiers.org/hco/3/GRCh38#36761058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111272324-C-A

36761340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111272047-T-C

36761343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111272044-T-C

36761498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111271890-C-T

http://identifiers.org/hco/3/GRCh38#36761510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111271878-C-A

36761510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111271878-C-T

36761578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111271819-A-T

36761634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111271766-A-G

http://identifiers.org/hco/3/GRCh38#36761676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111271730-A-C

36762379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111270014-T-C

36762736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111269659-A-G

36762758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111269637-T-C

36762858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111269577-G-T

36762966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111269467-C-G

36763016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111269420-C-T

36763094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111269342-C-T

36763102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111269331-C-T

36763117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111269316-T-C

36763162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111269290-G-C

36763274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111269186-C-G

36763507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111268959-T-A

36763660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111268837-G-A

36764027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: intron variant
orthologous variants: 111268531-C-T

http://identifiers.org/hco/3/GRCh38#36764217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111268383-C-A

36764217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111268383-C-G

36764217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111268383-C-T

36764229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111268371-G-A

36764229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: missense variant
orthologous variants: 111268371-G-T

36764267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5 prime UTR variant
orthologous variants: 111268344-G-A

36764267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5 prime UTR variant
orthologous variants: 111268344-G-T

36764336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 111268272-G-T

36764352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 111268258-G-A

36764352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 111268258-G-T

36764375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5 prime UTR variant
orthologous variants: 111268234-G-A

36764375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5 prime UTR variant
orthologous variants: 111268234-G-T

http://identifiers.org/hco/3/GRCh38#36764376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#111268233-C-A

36764376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 19005
most severe consequence: 5 prime UTR variant
orthologous variants: 111268233-C-T