67614672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86256646-T-A

67614967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86256872-T-C

http://identifiers.org/hco/4/GRCh38#67614980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86256884-C-A

67615020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86256923-G-C

67615020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86256923-G-T

67615111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86256982-A-G

67615219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86257029-A-G

67615444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86257127-A-G

67615764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86257335-G-A

67615764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86257335-G-T

67615927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86257507-A-G

67615927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86257507-A-T

67616143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86257692-C-G

67616215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86257899-T-C

67616215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86257899-T-G

67616425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86258138-G-C

http://identifiers.org/hco/4/GRCh38#67616467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86258181-C-A

67616472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86258186-G-T

http://identifiers.org/hco/4/GRCh38#67616681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86258377-A-C

67616681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86258377-A-T

67616683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86258379-T-C

67616687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86258383-G-A

67616687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86258383-G-C

http://identifiers.org/hco/4/GRCh38#67616796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86258490-C-A

67617404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86259044-G-A

67617654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86259259-T-C

67617760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86259346-G-T

67617773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86259359-T-G

67617814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86259394-A-G

67618059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86259641-A-T

http://identifiers.org/hco/4/GRCh38#67618082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86259665-C-A

67618082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86259665-C-T

http://identifiers.org/hco/4/GRCh38#67618260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86259821-A-C

http://identifiers.org/hco/4/GRCh38#67618352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86259902-C-A

67618352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86259902-C-G

67618617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86260154-T-C

http://identifiers.org/hco/4/GRCh38#67618763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86260296-C-A

67618763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86260296-C-G

67618834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86260364-T-C

67618854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3 prime UTR variant
orthologous variants: 86260384-G-T

67618905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 86260432-A-G

67618905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 86260432-A-T

67619039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 86260554-C-T

http://identifiers.org/hco/4/GRCh38#67619204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86260715-C-A

67619204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86260715-C-T

67619217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86260726-C-T

67620208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86262205-T-C

67620874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86262611-T-C

67620912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86262651-C-T

67622745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86265804-T-A

67622745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86265804-T-C

67622814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86265867-T-C

67622818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86265870-G-A

67622818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86265870-G-T

http://identifiers.org/hco/4/GRCh38#67622920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86265972-C-A

67622920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 86265972-C-T

67622962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86266011-C-T

67623053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86266087-C-T

http://identifiers.org/hco/4/GRCh38#67623283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86267334-C-A

67623283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86267334-C-T

67623403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86267546-A-G

67623788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86268047-G-A

67623914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86268180-A-G

67624191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 86268452-A-G

67624307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86268566-T-C

http://identifiers.org/hco/4/GRCh38#67624340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86268597-A-C

67624358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86268615-G-A

67624358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86268615-G-C

67624358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86268615-G-T

http://identifiers.org/hco/4/GRCh38#67624900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86270092-C-A

67624900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86270092-C-T

67624957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 86270133-A-G

67625069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 86270239-G-C

67625143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 86270313-G-A

67625216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86270382-T-C

67625358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86270661-G-A

http://identifiers.org/hco/4/GRCh38#67625381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86270696-C-A

http://identifiers.org/hco/4/GRCh38#67626302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86272117-C-A

67626302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86272117-C-T

http://identifiers.org/hco/4/GRCh38#67626412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86272222-C-A

67626412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: missense variant
orthologous variants: 86272222-C-G

67626620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86272443-T-A

67627567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86273278-G-A

67627844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86273515-T-C

http://identifiers.org/hco/4/GRCh38#67627870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86273556-A-C

67627871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86273557-G-T

67627875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86273567-T-G

http://identifiers.org/hco/4/GRCh38#67627971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86273632-A-C

67628969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86274227-A-T

67629026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86274284-C-G

67629026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86274284-C-T

67629128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 86274385-A-G

67629952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86274928-G-A

67630255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275224-A-G

67630290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275259-A-G

67630382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275449-A-G

67630382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275449-A-T

67630450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275543-T-C

67630451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275544-T-A

67630451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275544-T-C

67630451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275544-T-G

67630457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 86275550-A-G

67630457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, stop_gained
orthologous variants: 86275550-A-T

http://identifiers.org/hco/4/GRCh38#67630555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86275652-A-C

67630555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275652-A-G

67630648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275743-T-C

67630648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275743-T-G

67630874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275955-G-T

67630890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86275971-T-C

http://identifiers.org/hco/4/GRCh38#67631920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86276751-A-C

http://identifiers.org/hco/4/GRCh38#67631925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86276756-A-C

67631955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86276786-T-C

http://identifiers.org/hco/4/GRCh38#67632014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86276848-C-A

67632014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86276848-C-G

http://identifiers.org/hco/4/GRCh38#67632039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86276876-A-C

67632047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86276884-A-G

67632049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86276886-G-T

67632100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86276917-T-C

67632192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86276948-C-G

67632192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86276948-C-T

http://identifiers.org/hco/4/GRCh38#67632267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86277009-C-A

67632276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86277018-C-T

67633138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86278384-A-G

67633269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86279001-T-C

67633471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 86279198-C-T

67633507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86279236-T-C

http://identifiers.org/hco/4/GRCh38#67633617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86279343-C-A

67633617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86279343-C-T

67633621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86279347-T-C

67633733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86279665-G-C

67633770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86279786-A-G

67634115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86280178-G-A

67634115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86280178-G-T

67634339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86280391-A-G

67634718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86280718-T-C

67634743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86280745-T-C

67634772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86280773-T-A

67635334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86282715-A-G

67635334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86282715-A-T

67635369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86282744-A-G

67635388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86282764-G-T

67635453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 86282833-A-G

http://identifiers.org/hco/4/GRCh38#67635504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86282884-C-A

67635504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: missense variant
orthologous variants: 86282884-C-G

http://identifiers.org/hco/4/GRCh38#67635653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86283051-C-A

67635655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86283053-G-A

67635655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86283053-G-T

67635670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86283067-G-A

67635670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86283067-G-C

67635670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86283067-G-T

67638719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86283908-G-A

67638924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86284149-A-G

67639073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: missense variant
orthologous variants: 86284298-T-C

67640166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86284703-A-G

67640424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86284929-T-C

67640519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86285047-G-T

67640533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86285061-G-A

67640594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86285141-A-G

67640655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86285275-G-A

http://identifiers.org/hco/4/GRCh38#67641222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86285747-C-A

67641222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: missense variant
orthologous variants: 86285747-C-T

67641655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86286352-A-G

67644269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86287650-T-G

67644400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86287786-C-T

67644405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86287791-C-T

67644665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86288181-T-C

67644665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86288181-T-G

67644997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86288602-T-G

67645026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86288631-T-A

http://identifiers.org/hco/4/GRCh38#67645338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86288877-C-A

67645357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86288895-T-C

67645416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86288947-T-C

67646022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 86289491-A-G

http://identifiers.org/hco/4/GRCh38#67646139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86289594-C-A

67646359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86289902-T-C

67646364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86289907-T-G

http://identifiers.org/hco/4/GRCh38#67646621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86290150-A-C

67646657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86290187-T-C

67646681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86290208-T-C

67646838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86290372-T-A

67646877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86290418-A-G

67646894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86290430-A-G

67646941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86290470-A-G

67648838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86291928-A-T

http://identifiers.org/hco/4/GRCh38#67648973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86292094-A-C

67648973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86292094-A-T

67649080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: synonymous variant
orthologous variants: 86292206-A-T

67649176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: synonymous variant
orthologous variants: 86292302-A-G

67649188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: synonymous variant
orthologous variants: 86292314-C-T

http://identifiers.org/hco/4/GRCh38#67649268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86292394-A-C

http://identifiers.org/hco/4/GRCh38#67649353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86292494-C-A

67649356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86292497-A-T

67661911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86294657-T-C

67661990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86294740-T-C

67661996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86294746-G-A

67661996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86294746-G-T

67662041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 86294786-T-C

67662182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 86294927-T-C

67662259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 86295004-C-T

67662313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: 86295051-G-T

http://identifiers.org/hco/4/GRCh38#67662347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86295068-A-C

67662852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86295261-T-A

67662852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86295261-T-C

67663021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86295422-G-A

67663021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86295422-G-T

67663043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86295444-G-A

67663043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86295444-G-T

67663117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86295642-A-G

http://identifiers.org/hco/4/GRCh38#67663526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86296290-C-A

67664056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296886-G-A

67664056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86296886-G-T

67664579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86297238-G-A

67664863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86297470-T-G

67664906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86297506-C-T

67664957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86297550-T-C

67665037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86297698-T-G

http://identifiers.org/hco/4/GRCh38#67665138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86297806-C-A

67665138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86297806-C-T

67665149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86297832-T-C

67665150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86297833-G-A

67665150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86297833-G-T

67665371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86298020-T-A

67665371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86298020-T-C

67665371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86298020-T-G

67667786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86299886-C-T

http://identifiers.org/hco/4/GRCh38#67667877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86299969-C-A

67667877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86299969-C-T

67668195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300229-T-C

67668397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300272-G-A

67668436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300310-G-T

67668466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300340-T-C

67670556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86300771-A-T

67670587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86300802-G-C

67670608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300821-A-G

http://identifiers.org/hco/4/GRCh38#67670610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86300823-C-A

67670622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300829-T-G

67670630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300837-T-A

67670630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86300837-T-C

67671020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301202-A-G

67671190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301362-G-T

67671197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86301370-T-C

67673587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86302093-G-T

67674279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86302947-C-T

67674302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86302970-G-A

67674433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86303055-A-G

http://identifiers.org/hco/4/GRCh38#67674471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86303092-A-C

67674530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86303156-G-A

67677577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86307034-G-A

67677577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86307034-G-T

67677953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86307379-C-G

http://identifiers.org/hco/4/GRCh38#67678093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86307545-A-C

67678430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 86308129-T-C

67678588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308290-T-C

67678595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308297-T-C

67678595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308297-T-G

67678598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308300-T-C

67678672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308371-T-C

67678905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86308850-G-A

http://identifiers.org/hco/4/GRCh38#67679048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86308981-C-A

67679454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86309347-C-G

67679459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86309352-C-T

67679664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86310056-T-C

67679664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86310056-T-G

67679832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86310206-T-C

67680014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86310376-T-C

67680643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311141-C-T

67680670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311168-C-T

67681065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311473-T-C

http://identifiers.org/hco/4/GRCh38#67681505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86311874-C-A

67681505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311874-C-T

67681519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86311890-A-G

http://identifiers.org/hco/4/GRCh38#67681619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86311994-C-A

http://identifiers.org/hco/4/GRCh38#67681641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86312016-A-C

67681641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312016-A-G

67681662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312035-A-G

67681816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312193-G-A

67681831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312252-T-A

http://identifiers.org/hco/4/GRCh38#67682079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86312512-C-A

67682079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312512-C-T

67682086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312519-G-C

67682086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312519-G-T

67682264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312700-A-G

67682264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312700-A-T

67682312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312746-G-A

67682312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86312746-G-T

http://identifiers.org/hco/4/GRCh38#67682836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86313249-C-A

67682836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86313249-C-T

67683211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86313635-C-T

67696711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 86318485-G-A

67696711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 86318485-G-T

67699998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86319437-G-A

67700128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86319677-T-C

http://identifiers.org/hco/4/GRCh38#67700175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86319745-A-C

67700771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86320260-G-A

http://identifiers.org/hco/4/GRCh38#67700909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86320371-C-A

67700909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86320371-C-T

67701108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86320586-G-A

67701108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86320586-G-T

http://identifiers.org/hco/4/GRCh38#67701144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86320622-C-A

67701144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86320622-C-G

67701148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86320628-T-A

67701148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86320628-T-C

67701148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 86320628-T-G

67701150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 5 prime UTR variant
orthologous variants: 86320630-G-A

67701150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 5 prime UTR variant
orthologous variants: 86320630-G-C

67701150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25581
most severe consequence: 5 prime UTR variant
orthologous variants: 86320630-G-T