55113974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3 prime UTR variant
orthologous variants: 113227886-G-A

55113974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3 prime UTR variant
orthologous variants: 113227886-G-T

55114022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3 prime UTR variant
orthologous variants: 113227839-G-A

55114276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: missense variant
orthologous variants: 113227609-T-G

http://identifiers.org/hco/5/GRCh38#55114383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113227519-A-C

55114404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113227500-T-G

55114455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113227452-T-C

55114866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113226995-T-C

55115445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113226459-T-C

55115659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113226274-A-G

55115661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113226272-C-T

55115796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113226140-G-A

55115979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113226014-A-G

55115981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113226012-A-T

55116961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113224366-G-A

55117100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113224238-G-A

55118900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113221727-A-G

55118947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113221665-A-G

55119220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113221417-C-T

55119652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113220707-T-G

55119716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: 113220653-T-C

http://identifiers.org/hco/5/GRCh38#55119748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113220623-C-A

55119876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 113220504-T-C

55119991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113220388-G-A

55119991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113220388-G-T

55120027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113220352-A-G

55120027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113220352-A-T

55120082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113220296-G-A

55120092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113220286-A-G

55120092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113220286-A-T

55120302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113220011-C-T

55120615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219759-T-A

55120615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219759-T-C

55120615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219759-T-G

http://identifiers.org/hco/5/GRCh38#55120618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113219756-A-C

55120618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219756-A-G

http://identifiers.org/hco/5/GRCh38#55120640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113219736-C-A

55120640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219736-C-T

55120647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219729-G-A

55120647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219729-G-T

55120676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219715-A-T

http://identifiers.org/hco/5/GRCh38#55120699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113219689-C-A

55120709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219679-A-T

55121195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219228-G-A

http://identifiers.org/hco/5/GRCh38#55121248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113219176-C-A

55121283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219141-C-T

55121286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219138-G-A

55121286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113219138-G-C

55121664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113218606-T-C

55121862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113218400-G-A

55124813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 113217785-G-A

55124813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 113217785-G-C

http://identifiers.org/hco/5/GRCh38#55125075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113217513-C-A

http://identifiers.org/hco/5/GRCh38#55125147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113217451-C-A

http://identifiers.org/hco/5/GRCh38#55125159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113217435-C-A

55125172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113217422-A-G

55125178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113217416-G-A

55125178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113217416-G-C

http://identifiers.org/hco/5/GRCh38#55125179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113217415-A-C

55125179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113217415-A-G

55125183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113217411-T-A

55125183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113217411-T-C

http://identifiers.org/hco/5/GRCh38#55125212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113217383-A-C

55127113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113216677-T-C

55127145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113216653-T-C

55127184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113216613-T-C

55127229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113216536-T-A

55127229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113216536-T-C

55127339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113216427-C-T

55127356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113216410-A-G

55127399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113216357-C-T

55127440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113216318-T-C

55127452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113216305-T-A

55127452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113216305-T-C

55127719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215903-T-C

55127816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215810-T-C

55127837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215789-T-C

55127855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215771-T-C

55128016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215667-A-G

55128087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215625-C-T

55128194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215518-T-C

http://identifiers.org/hco/5/GRCh38#55128253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113215460-C-A

55128273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215452-A-G

55128292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215436-T-A

55128292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215436-T-C

http://identifiers.org/hco/5/GRCh38#55128302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113215426-C-A

55128302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215426-C-T

http://identifiers.org/hco/5/GRCh38#55128304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113215424-C-A

55128304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215424-C-T

http://identifiers.org/hco/5/GRCh38#55128309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113215419-C-A

55128309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215419-C-T

55128310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215418-T-A

55128339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215392-T-C

55128339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215392-T-G

55128345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215386-A-T

55128357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215377-A-G

55128370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215366-G-T

55128403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215337-A-G

55128422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 113215324-T-C

55128462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113215284-C-T

55128556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113215190-T-C

55128562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113215184-A-G

http://identifiers.org/hco/5/GRCh38#55128668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113215078-A-C

55128690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215056-A-G

55128691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215055-G-A

55128691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215055-G-T

55128710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215036-T-C

55128710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215036-T-G

55128738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215008-G-A

55128738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113215008-G-T

55128907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113214842-T-C

55128951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113214798-T-G

55129016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113214737-A-G

55129046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113214278-T-C

55132269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113209491-T-C

55132439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113209359-T-G

55132842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113209024-A-G

55133255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208652-C-T

55133266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208640-A-G

http://identifiers.org/hco/5/GRCh38#55133293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113208625-C-A

55133293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208625-C-T

55133338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208574-T-C

55133354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208558-A-G

55133360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208552-G-A

55133360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208552-G-T

55133362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208550-A-G

55133362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208550-A-T

55133369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208543-T-C

55133369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208543-T-G

55133371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208541-G-A

55133371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208541-G-T

55133403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208509-A-G

55133403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208509-A-T

55133450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113208462-T-C

55133501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113208414-G-A

55133501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113208414-G-T

http://identifiers.org/hco/5/GRCh38#55133520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113208395-C-A

http://identifiers.org/hco/5/GRCh38#55133532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113208383-C-A

55133532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 113208383-C-T

http://identifiers.org/hco/5/GRCh38#55133553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113208362-C-A

55133553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208362-C-T

55133564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208351-T-C

55133640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208295-A-G

55133885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113208062-T-G

55134269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113207743-C-T

55134294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113207718-G-A

55134297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113207715-C-T

55134349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113207663-C-T

55135418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113205153-G-A

55135583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113204970-T-G

55139343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113201547-G-A

55139374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113201507-G-A

55139432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113201452-A-G

55139492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113201394-G-A

55139535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113201353-T-C

55139580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113201310-T-A

55139761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113201150-A-G

55140082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113201084-A-G

55140173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113201002-T-G

55140206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200969-G-T

55140260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200920-A-G

55140260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200920-A-T

http://identifiers.org/hco/5/GRCh38#55140295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113200885-C-A

55140295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200885-C-T

55140297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200883-A-G

55140389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113200787-A-G

55140409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: 113200767-T-C

55140416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200760-A-T

55140438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200738-T-C

http://identifiers.org/hco/5/GRCh38#55140470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113200706-A-C

55140470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200706-A-G

55140480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200698-A-G

http://identifiers.org/hco/5/GRCh38#55140503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113200675-C-A

55140590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200638-G-A

55140656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200582-T-C

http://identifiers.org/hco/5/GRCh38#55140805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113200455-A-C

55140843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200417-C-G

55140987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113200271-C-T

55142123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113198960-C-T

55142129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113198954-G-A

55142393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113198712-A-G

55142465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113198652-T-C

55142863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113198272-T-C

55142883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113198252-G-A

55143116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113198049-T-C

55143120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113198044-A-G

55143358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113196484-T-C

55143582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113196294-A-G

55143614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113196262-T-C

55144558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113194995-A-T

http://identifiers.org/hco/5/GRCh38#55144583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113194968-A-C

55144665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113194896-T-C

55145180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113194151-A-G

55145246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113194123-C-T

55145247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113194122-T-C

55145279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113194090-G-A

http://identifiers.org/hco/5/GRCh38#55145395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113193951-A-C

55145442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113193752-G-A

55145508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113193686-G-A

55146649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113192640-C-T

55146679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 113192610-C-T

55146685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 113192604-G-A

http://identifiers.org/hco/5/GRCh38#55146764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113192525-A-C

55146768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 113192521-G-C

55146797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 113192492-C-G

55146798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 113192491-A-G

55146798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 113192491-A-T

http://identifiers.org/hco/5/GRCh38#55146806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113192483-C-A

55146806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 113192483-C-G

55146806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 113192483-C-T

55146836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 113192453-A-T

55146850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 113192439-C-G

55146889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113192399-T-A

55146900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113192388-A-T

55146916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113192371-T-A

55146918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113192369-C-T

55146923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113192364-A-G

55151357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113192013-G-A

55151522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113191909-A-G

55151617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113191817-C-T

55152083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113191345-G-A

55152196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113191239-C-T

55152198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113191237-C-G

55152272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113191167-A-G

55152432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113191027-G-A

55154575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113188928-G-T

55155865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113187011-C-G

55157003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113186553-G-T

55157377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113186227-T-C

55157459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113186197-A-G

55157608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113185675-A-G

55157712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113185574-A-G

55157819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113185479-G-A

55157884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113185417-T-A

55157907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113185396-A-G

55158743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113184350-A-G

55158838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113184270-T-A

55158899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113184213-G-A

55158920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113184193-G-A

55159545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113183530-A-G

55160022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113183067-T-C

55160184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113182916-T-C

55160450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113182658-T-A

55160676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113182463-A-G

55160891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113182340-A-G

55160936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113182296-G-T

55160972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113182247-G-A

55161050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant, synonymous_variant, undefined
orthologous variants: 113182169-A-G

http://identifiers.org/hco/5/GRCh38#55161325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113181878-C-A

55161325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113181878-C-G

55161325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113181878-C-T

55163904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113180000-G-A

55163904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113180000-G-C

55164241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113179638-G-A

55164377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113179612-T-C

55164397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113179600-A-G

55164543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113179455-G-A

55164543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113179455-G-C

55164543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113179455-G-T

55164666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113179349-T-A

55165140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113179024-A-G

55165232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113178944-C-G

55166179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113178076-A-G

55166183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113178072-G-T

55166187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113178068-G-A

55166187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113178068-G-T

55166231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113178014-A-G

http://identifiers.org/hco/5/GRCh38#55166358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113177896-C-A

55166358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113177896-C-T

55166418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113177843-T-C

http://identifiers.org/hco/5/GRCh38#55166565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113177712-C-A

55166565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113177712-C-T

55169019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113175891-A-G

55169238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113174990-C-T

55169317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113174909-T-C

55169372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113174856-A-T

55169656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113174593-G-T

55169823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113174540-T-A

55169911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113174507-A-G

55169978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113174465-G-A

55170388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113174269-C-T

55170444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113174227-A-G

55170570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113174118-G-A

55170673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113174014-A-T

55171210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113173453-G-C

55172139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113172718-C-G

http://identifiers.org/hco/5/GRCh38#55172350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113172526-C-A

55172358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113172518-T-C

55172372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113172507-G-A

55172372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113172507-G-T

55172419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113172444-G-A

55172419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 113172444-G-T

55172551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113172342-A-G

55172551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113172342-A-T

55172587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant, undefined
orthologous variants: 113172309-C-T

55172698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113172200-T-C

55172701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113172197-T-C

55172777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113172136-G-A

55172777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113172136-G-C

55172777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113172136-G-T

http://identifiers.org/hco/5/GRCh38#55172817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113172098-C-A

55172817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113172098-C-T

55172923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113171988-A-G

55172932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 113171979-A-G

55173025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 113171885-G-A

55173066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 113171864-A-G

55173086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 113171849-G-A

55173086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 113171849-G-T

http://identifiers.org/hco/5/GRCh38#55173101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#113171834-C-A

55173101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 113171834-C-T

http://identifiers.org/hco/5/GRCh38#55173131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#113171805-A-C

55173131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 113171805-A-G

55173142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 113171794-T-C

55173142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24222
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 113171794-T-G